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membrane protein folding</title> <meta name="description" content="Search results for: integral membrane protein folding"> <meta name="keywords" content="integral membrane protein folding"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="integral membrane protein folding"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 4153</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: integral membrane protein folding</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4153</span> Structural and Functional Comparison of Untagged and Tagged EmrE Protein</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=S.%20Junaid%20S.%20Qazi">S. Junaid S. Qazi</a>, <a href="https://publications.waset.org/abstracts/search?q=Denice%20C.%20Bay"> Denice C. Bay</a>, <a href="https://publications.waset.org/abstracts/search?q=Raymond%20Chew"> Raymond Chew</a>, <a href="https://publications.waset.org/abstracts/search?q=Raymond%20J.%20Turner"> Raymond J. Turner</a> </p> <p class="card-text"><strong>Abstract:</strong></p> EmrE, a member of the small multidrug resistance protein family in bacteria is considered to be the archetypical member of its family. It confers host resistance to a wide variety of quaternary cation compounds (QCCs) driven by proton motive force. Generally, purification yield is a challenge in all membrane proteins because of the difficulties in their expression, isolation and solubilization. EmrE is extremely hydrophobic which make the purification yield challenging. We have purified EmrE protein using two different approaches: organic solvent membrane extraction and hexahistidine (his6) tagged Ni-affinity chromatographic methods. We have characterized changes present between ligand affinity of untagged and his6-tagged EmrE proteins in similar membrane mimetic environments using biophysical experimental techniques. Purified proteins were solubilized in a buffer containing n-dodecyl-β-D-maltopyranoside (DDM) and the conformations in the proteins were explored in the presence of four QCCs, methyl viologen (MV), ethidium bromide (EB), cetylpyridinium chloride (CTP) and tetraphenyl phosphonium (TPP). SDS-Tricine PAGE and dynamic light scattering (DLS) analysis revealed that the addition of QCCs did not induce higher multimeric forms of either proteins at all QCC:EmrE molar ratios examined under the solubilization conditions applied. QCC binding curves obtained from the Trp fluorescence quenching spectra, gave the values of dissociation constant (Kd) and maximum specific one-site binding (Bmax). Lower Bmax values to QCCs for his6-tagged EmrE shows that the binding sites remained unoccupied. This lower saturation suggests that the his6-tagged versions provide a conformation that prevents saturated binding. Our data demonstrate that tagging an integral membrane protein can significantly influence the protein. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=small%20multidrug%20resistance%20%28SMR%29%20protein" title="small multidrug resistance (SMR) protein">small multidrug resistance (SMR) protein</a>, <a href="https://publications.waset.org/abstracts/search?q=EmrE" title=" EmrE"> EmrE</a>, <a href="https://publications.waset.org/abstracts/search?q=integral%20membrane%20protein%20folding" title=" integral membrane protein folding"> integral membrane protein folding</a>, <a href="https://publications.waset.org/abstracts/search?q=quaternary%20ammonium%20compounds%20%28QAC%29" title=" quaternary ammonium compounds (QAC)"> quaternary ammonium compounds (QAC)</a>, <a href="https://publications.waset.org/abstracts/search?q=quaternary%20cation%20compounds%20%28QCC%29" title=" quaternary cation compounds (QCC)"> quaternary cation compounds (QCC)</a>, <a href="https://publications.waset.org/abstracts/search?q=nickel%20affinity%20chromatography" title=" nickel affinity chromatography"> nickel affinity chromatography</a>, <a href="https://publications.waset.org/abstracts/search?q=hexahistidine%20%28His6%29%20tag" title=" hexahistidine (His6) tag"> hexahistidine (His6) tag</a> </p> <a href="https://publications.waset.org/abstracts/36260/structural-and-functional-comparison-of-untagged-and-tagged-emre-protein" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/36260.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">379</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4152</span> In vitro Protein Folding and Stability Using Thermostable Exoshells </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Siddharth%20Deshpande">Siddharth Deshpande</a>, <a href="https://publications.waset.org/abstracts/search?q=Nihar%20Masurkar"> Nihar Masurkar</a>, <a href="https://publications.waset.org/abstracts/search?q=Vallerinteavide%20Mavelli%20Girish"> Vallerinteavide Mavelli Girish</a>, <a href="https://publications.waset.org/abstracts/search?q=Malan%20Desai"> Malan Desai</a>, <a href="https://publications.waset.org/abstracts/search?q=Chester%20Drum"> Chester Drum</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Folding and stabilization of recombinant proteins remain a consistent challenge for industrial and therapeutic applications. Proteins derived from thermophilic bacteria often have superior expression and stability qualities. To develop a generalizable approach to protein folding and stabilization, we tested the hypothesis that wrapping a thermostable exoshell around a protein substrate would aid folding and impart thermostable qualities to the internalized substrate. To test the effect of internalizing a protein within a thermostable exoshell (tES), we tested in vitro folding and stability using green fluorescent protein (GFPuv), horseradish peroxidase (HRP) and renilla luciferase (rLuc). The 8nm interior volume of a thermostable ferritin assembly was engineered to accommodate foreign proteins and either present a positive, neutral or negative interior charge environment. We further engineered the tES complex to reversibly assemble and disassemble with pH titration. Template proteins were expressed as inclusion bodies and an in vitro folding protocol was developed that forced proteins to fold inside a single tES. Functional yield was improved 100-fold, 100-fold and 150-fold with use of tES for GFPuv, HRP and rLuc respectively and was highly dependent on the internal charge environment of the tES. After folding, functional proteins could be released from the tES folding cavity using size exclusion chromatography at pH 5.8. Internalized proteins were tested for improved stability against thermal, organic, urea and guanidine denaturation. Our results demonstrated that thermostable exoshells can efficiently refold and stabilize inactive aggregates into functional proteins. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=thermostable%20shell" title="thermostable shell">thermostable shell</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20vitro%20folding" title=" in vitro folding"> in vitro folding</a>, <a href="https://publications.waset.org/abstracts/search?q=stability" title=" stability"> stability</a>, <a href="https://publications.waset.org/abstracts/search?q=functional%20yield" title=" functional yield"> functional yield</a> </p> <a href="https://publications.waset.org/abstracts/72637/in-vitro-protein-folding-and-stability-using-thermostable-exoshells" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/72637.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">249</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4151</span> Biophysical Characterization of Archaeal Cyclophilin Like Chaperone Protein</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Vineeta%20Kaushik">Vineeta Kaushik</a>, <a href="https://publications.waset.org/abstracts/search?q=Manisha%20Goel"> Manisha Goel</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chaperones are proteins that help other proteins fold correctly, and are found in all domains of life i.e., prokaryotes, eukaryotes and archaea. Various comparative genomic studies have suggested that the archaeal protein folding machinery appears to be highly similar to that found in eukaryotes. In case of protein folding; slow rotation of peptide prolyl-imide bond is often the rate limiting step. Formation of the prolyl-imide bond during the folding of a protein requires the assistance of other proteins, termed as peptide prolyl cis-trans isomerases (PPIases). Cyclophilins constitute the class of peptide prolyl isomerases with a wide range of biological function like protein folding, signaling and chaperoning. Most of the cyclophilins exhibit PPIase enzymatic activity and play active role in substrate protein folding which classifies them as a category of molecular chaperones. Till date, there is not very much data available in the literature on archaeal cyclophilins. We aim to compare the structural and biochemical features of the cyclophilin protein from within the three domains to elucidate the features affecting their stability and enzyme activity. In the present study, we carry out in-silico analysis of the cyclophilin proteins to predict their conserved residues, sites under positive selection and compare these proteins to their bacterial and eukaryotic counterparts to predict functional divergence. We also aim to clone and express these proteins in heterologous system and study their biophysical characteristics in detail using techniques like CD and fluorescence spectroscopy. Overall we aim to understand the features contributing to the folding, stability and dynamics of the archaeal cyclophilin proteins. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biophysical%20characterization" title="biophysical characterization">biophysical characterization</a>, <a href="https://publications.waset.org/abstracts/search?q=x-ray%20crystallography" title=" x-ray crystallography"> x-ray crystallography</a>, <a href="https://publications.waset.org/abstracts/search?q=chaperone-like%20activity" title=" chaperone-like activity"> chaperone-like activity</a>, <a href="https://publications.waset.org/abstracts/search?q=cyclophilin" title=" cyclophilin"> cyclophilin</a>, <a href="https://publications.waset.org/abstracts/search?q=PPIase%20activity" title=" PPIase activity"> PPIase activity</a> </p> <a href="https://publications.waset.org/abstracts/67459/biophysical-characterization-of-archaeal-cyclophilin-like-chaperone-protein" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/67459.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">213</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4150</span> Human LACE1 Functions Pro-Apoptotic and Interacts with Mitochondrial YME1L Protease</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lukas%20Stiburek">Lukas Stiburek</a>, <a href="https://publications.waset.org/abstracts/search?q=Jana%20Cesnekova"> Jana Cesnekova</a>, <a href="https://publications.waset.org/abstracts/search?q=Josef%20Houstek"> Josef Houstek</a>, <a href="https://publications.waset.org/abstracts/search?q=Jiri%20Zeman"> Jiri Zeman</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Cellular function depends on mitochondrial function and integrity that is therefore maintained by several classes of proteins possessing chaperone and/or proteolytic activities. In this work, we focused on characterization of LACE1 (lactation elevated 1) function in mitochondrial protein homeostasis maintenance. LACE1 is the human homologue of yeast mitochondrial Afg1 ATPase, a member of SEC18-NSF, PAS1, CDC48-VCP, TBP family. Yeast Afg1 was shown to be involved in mitochondrial complex IV biogenesis, and based on its similarity with CDC48 (p97/VCP) it was suggested to facilitate extraction of polytopic membrane proteins. Here we show that LACE1, which is a mitochondrial integral membrane protein, exists as part of three complexes of approx. 140, 400 and 500 kDa and is essential for maintenance of fused mitochondrial reticulum and lamellar cristae morphology. Using affinity purification of LACE1-FLAG expressed in LACE1 knockdown background we show that the protein physically interacts with mitochondrial inner membrane protease YME1L. We further show that human LACE1 exhibits significant pro-apoptotic activity and that the protein is required for normal function of the mitochondrial respiratory chain. Thus, our work establishes LACE1 as a novel factor with the crucial role in mitochondrial homeostasis maintenance. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=LACE1" title="LACE1">LACE1</a>, <a href="https://publications.waset.org/abstracts/search?q=mitochondria" title=" mitochondria"> mitochondria</a>, <a href="https://publications.waset.org/abstracts/search?q=apoptosis" title=" apoptosis"> apoptosis</a>, <a href="https://publications.waset.org/abstracts/search?q=protease" title=" protease"> protease</a> </p> <a href="https://publications.waset.org/abstracts/46195/human-lace1-functions-pro-apoptotic-and-interacts-with-mitochondrial-yme1l-protease" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46195.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">313</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4149</span> Insights of Interaction Studies between HSP-60, HSP-70 Proteins and HSF-1 in Bubalus bubalis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ravinder%20Singh">Ravinder Singh</a>, <a href="https://publications.waset.org/abstracts/search?q=C%20Rajesh"> C Rajesh</a>, <a href="https://publications.waset.org/abstracts/search?q=Saroj%20Badhan"> Saroj Badhan</a>, <a href="https://publications.waset.org/abstracts/search?q=Shailendra%20Mishra"> Shailendra Mishra</a>, <a href="https://publications.waset.org/abstracts/search?q=Ranjit%20Singh%20Kataria"> Ranjit Singh Kataria</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Heat shock protein 60 and 70 are crucial chaperones that guide appropriate folding of denatured proteins under heat stress conditions. HSP60 and HSP70 provide assistance in correct folding of a multitude of denatured proteins. The heat shock factors are the family of some transcription factors which controls the regulation of gene expression of proteins involved in folding of damaged or improper folded proteins during stress conditions. Under normal condition heat shock proteins bind with HSF-1 and act as its repressor as well as aids in maintaining the HSF-1’s nonactive and monomeric confirmation. The experimental protein structure for all these proteins in Bubalus bubalis is not known till date. Therefore computational approach was explored to identify three-dimensional structure analysis of all these proteins. In this study, an extensive in silico analysis has been performed including sequence comparison among species to comparative modeling of Bubalus bubalis HSP60, HSP70 and HSF-1 protein. The stereochemical properties of proteins were assessed by utilizing several scrutiny bioinformatics tools to ensure model accuracy. Further docking approach was used to study interactions between Heat shock proteins and HSF-1. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bubalus%20bubalis" title="Bubalus bubalis">Bubalus bubalis</a>, <a href="https://publications.waset.org/abstracts/search?q=comparative%20modelling" title=" comparative modelling"> comparative modelling</a>, <a href="https://publications.waset.org/abstracts/search?q=docking" title=" docking"> docking</a>, <a href="https://publications.waset.org/abstracts/search?q=heat%20shock%20protein" title=" heat shock protein"> heat shock protein</a> </p> <a href="https://publications.waset.org/abstracts/64431/insights-of-interaction-studies-between-hsp-60-hsp-70-proteins-and-hsf-1-in-bubalus-bubalis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/64431.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">322</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4148</span> Membrane Spanning DNA Origami Nanopores for Protein Translocation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Genevieve%20Pugh">Genevieve Pugh</a>, <a href="https://publications.waset.org/abstracts/search?q=Johnathan%20Burns"> Johnathan Burns</a>, <a href="https://publications.waset.org/abstracts/search?q=Stefan%20Howorka"> Stefan Howorka</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Single-molecule sensing via protein nanopores has achieved a step-change in portable and label-free DNA sequencing. However, protein pores of both natural or engineered origin are not able to produce the tunable diameters needed for effective protein sensing. Here, we describe a generic strategy to build synthetic DNA nanopores that are wide enough to accommodate folded protein. The pores are composed of interlinked DNA duplexes and carry lipid anchors to achieve the required membrane insertion. Our demonstrator pore has a contiguous cross-sectional channel area of 50 nm2 which is 6-times larger than the largest protein pore. Consequently, transport of folded protein across bilayers is possible. The modular design is amenable for different pore dimensions and can be adapted for protein sensing or to create molecular gates in synthetic biology. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biosensing" title="biosensing">biosensing</a>, <a href="https://publications.waset.org/abstracts/search?q=DNA%20nanotechnology" title=" DNA nanotechnology"> DNA nanotechnology</a>, <a href="https://publications.waset.org/abstracts/search?q=DNA%20origami" title=" DNA origami"> DNA origami</a>, <a href="https://publications.waset.org/abstracts/search?q=nanopore%20sensing" title=" nanopore sensing"> nanopore sensing</a> </p> <a href="https://publications.waset.org/abstracts/78556/membrane-spanning-dna-origami-nanopores-for-protein-translocation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/78556.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">323</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4147</span> Alternative Splicing of an Arabidopsis Gene, At2g24600, Encoding Ankyrin-Repeat Protein</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=H.%20Sakamoto">H. Sakamoto</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Kurosawa"> S. Kurosawa</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Suzuki"> M. Suzuki</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Oguri"> S. Oguri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In Arabidopsis, several genes encoding proteins with ankyrin repeats and trans-membrane domains (AtANKTM) have been identified as mediators of biotic and abiotic stress responses. It has been known that the expression of an AtANKTM gene, At2g24600, is induced in response to abiotic stress and that there are four splicing variants derived from this locus. In this study, by RT-PCR and sequencing analysis, an unknown splicing variant of the At2g24600 transcript was identified. Based on differences in the predicted amino acid sequences, the five splicing variants are divided into three groups. The three predicted proteins are highly homologous, yet have different numbers of ankyrin repeats and trans-membrane domains. It is generally considered that ankyrin repeats mediate protein-protein interaction and that the number of trans-membrane domains affects membrane topology of proteins. The protein variants derived from the At2g24600 locus may have different molecular functions each other. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alternative%20splicing" title="alternative splicing">alternative splicing</a>, <a href="https://publications.waset.org/abstracts/search?q=ankyrin%20repeats" title=" ankyrin repeats"> ankyrin repeats</a>, <a href="https://publications.waset.org/abstracts/search?q=trans-membrane%20domains" title=" trans-membrane domains"> trans-membrane domains</a>, <a href="https://publications.waset.org/abstracts/search?q=arabidopsis" title=" arabidopsis"> arabidopsis</a> </p> <a href="https://publications.waset.org/abstracts/6374/alternative-splicing-of-an-arabidopsis-gene-at2g24600-encoding-ankyrin-repeat-protein" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/6374.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">374</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4146</span> Predicting Aggregation Propensity from Low-Temperature Conformational Fluctuations</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamza%20Javar%20Magnier">Hamza Javar Magnier</a>, <a href="https://publications.waset.org/abstracts/search?q=Robin%20Curtis"> Robin Curtis</a> </p> <p class="card-text"><strong>Abstract:</strong></p> There have been rapid advances in the upstream processing of protein therapeutics, which has shifted the bottleneck to downstream purification and formulation. Finding liquid formulations with shelf lives of up to two years is increasingly difficult for some of the newer therapeutics, which have been engineered for activity, but their formulations are often viscous, can phase separate, and have a high propensity for irreversible aggregation1. We explore means to develop improved predictive ability from a better understanding of how protein-protein interactions on formulation conditions (pH, ionic strength, buffer type, presence of excipients) and how these impact upon the initial steps in protein self-association and aggregation. In this work, we study the initial steps in the aggregation pathways using a minimal protein model based on square-well potentials and discontinuous molecular dynamics. The effect of model parameters, including range of interaction, stiffness, chain length, and chain sequence, implies that protein models fold according to various pathways. By reducing the range of interactions, the folding- and collapse- transition come together, and follow a single-step folding pathway from the denatured to the native state2. After parameterizing the model interaction-parameters, we developed an understanding of low-temperature conformational properties and fluctuations, and the correlation to the folding transition of proteins in isolation. The model fluctuations increase with temperature. We observe a low-temperature point, below which large fluctuations are frozen out. This implies that fluctuations at low-temperature can be correlated to the folding transition at the melting temperature. Because proteins “breath” at low temperatures, defining a native-state as a single structure with conserved contacts and a fixed three-dimensional structure is misleading. Rather, we introduce a new definition of a native-state ensemble based on our understanding of the core conservation, which takes into account the native fluctuations at low temperatures. This approach permits the study of a large range of length and time scales needed to link the molecular interactions to the macroscopically observed behaviour. In addition, these models studied are parameterized by fitting to experimentally observed protein-protein interactions characterized in terms of osmotic second virial coefficients. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=protein%20folding" title="protein folding">protein folding</a>, <a href="https://publications.waset.org/abstracts/search?q=native-ensemble" title=" native-ensemble"> native-ensemble</a>, <a href="https://publications.waset.org/abstracts/search?q=conformational%20fluctuation" title=" conformational fluctuation"> conformational fluctuation</a>, <a href="https://publications.waset.org/abstracts/search?q=aggregation" title=" aggregation"> aggregation</a> </p> <a href="https://publications.waset.org/abstracts/18844/predicting-aggregation-propensity-from-low-temperature-conformational-fluctuations" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/18844.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">361</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4145</span> Folding Pathway and Thermodynamic Stability of Monomeric GroEL</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sarita%20Puri">Sarita Puri</a>, <a href="https://publications.waset.org/abstracts/search?q=Tapan%20K.%20Chaudhuri"> Tapan K. Chaudhuri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chaperonin GroEL is a tetradecameric Escherichia coli protein having identical subunits of 57 kDa. The elucidation of thermodynamic parameters related to stability for the native GroEL is not feasible as it undergoes irreversible unfolding because of its large size (800kDa) and multimeric nature. Nevertheless, it is important to determine the thermodynamic stability parameters for the highly stable GroEL protein as it helps in folding and holding of many substrate proteins during many cellular stresses. Properly folded monomers work as building-block for the formation of native tetradecameric GroEL. Spontaneous refolding behavior of monomeric GroEL makes it suitable for protein-denaturant interactions and thermodynamic stability based studies. The urea mediated unfolding is a three state process which means there is the formation of one intermediate state along with native and unfolded states. The heat mediated denaturation is a two-state process. The unfolding process is reversible as observed by the spontaneous refolding of denatured protein in both urea and head mediated refolding processes. Analysis of folding/unfolding data provides a measure of various thermodynamic stability parameters for the monomeric GroEL. The proposed mechanism of unfolding of monomeric GroEL is a three state process which involves formation of one stable intermediate having folded apical domain and unfolded equatorial, intermediate domains. Research in progress is to demonstrate the importance of specific residues in stability and oligomerization of GroEL protein. Several mutant versions of GroEL are under investigation to resolve the above mentioned issue. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=equilibrium%20unfolding" title="equilibrium unfolding">equilibrium unfolding</a>, <a href="https://publications.waset.org/abstracts/search?q=monomeric%20GroEl" title=" monomeric GroEl"> monomeric GroEl</a>, <a href="https://publications.waset.org/abstracts/search?q=spontaneous%20refolding" title=" spontaneous refolding"> spontaneous refolding</a>, <a href="https://publications.waset.org/abstracts/search?q=thermodynamic%20stability" title=" thermodynamic stability"> thermodynamic stability</a> </p> <a href="https://publications.waset.org/abstracts/67151/folding-pathway-and-thermodynamic-stability-of-monomeric-groel" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/67151.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">282</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4144</span> Interaction of Glycolipid S-TGA-1 with Bacteriorhodopsin and Its Functional Role </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Masataka%20Inada">Masataka Inada</a>, <a href="https://publications.waset.org/abstracts/search?q=Masanao%20Kinoshita"> Masanao Kinoshita</a>, <a href="https://publications.waset.org/abstracts/search?q=Nobuaki%20Matsumori"> Nobuaki Matsumori</a> </p> <p class="card-text"><strong>Abstract:</strong></p> It has been demonstrated that lipid molecules in biological membranes are responsible for the functionalization and structuration of membrane proteins. However, it is still unclear how the interaction of lipid molecules with membrane proteins is correlated with the function of the membrane proteins. Here we first developed an evaluation method for the interaction between membrane proteins and lipid molecules via surface plasmon resonance (SPR) analysis. Bacteriorhodopsin (bR), which was obtained by the culture of halobacteria, was used as a membrane protein. We prepared SPR sensor chips covered with self-assembled monolayer containing mercaptocarboxylic acids, and immobilized bR onto them. Then, we evaluated the interactions with various lipids that have different structures. As a result, the halobacterium-specific glycolipid S-TGA-1 was found to have much higher affinity with bRs than other lipids. This is probably due to not only hydrophobic and electrostatic interactions but also hydrogen bonds with sugar moieties in the glycolipid. Next, we analyzed the roles of the lipid in the structuration and functionalization of bR. CD analysis showed that S-TGA-1 could promote trimerization of bR monomers more efficiently than any other lipids. Flash photolysis further indicated that bR trimers formed by S-TGA-1 reproduced the photocyclic activity of bR in purple membrane, halobacterium-membrane. These results suggest that S-TGA-1 promotes trimerization of bR through strong interactions and consequently fulfills the bR’s function efficiently. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=membrane%20protein" title="membrane protein">membrane protein</a>, <a href="https://publications.waset.org/abstracts/search?q=lipid" title=" lipid"> lipid</a>, <a href="https://publications.waset.org/abstracts/search?q=interaction" title=" interaction"> interaction</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteriorhodopsin" title=" bacteriorhodopsin"> bacteriorhodopsin</a>, <a href="https://publications.waset.org/abstracts/search?q=glycolipid" title=" glycolipid"> glycolipid</a> </p> <a href="https://publications.waset.org/abstracts/72463/interaction-of-glycolipid-s-tga-1-with-bacteriorhodopsin-and-its-functional-role" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/72463.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">253</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4143</span> Quantifying the Protein-Protein Interaction between the Ion-Channel-Forming Colicin A and the Tol Proteins by Potassium Efflux in E. coli Cells</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fadilah%20Aleanizy">Fadilah Aleanizy</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Colicins are a family of bacterial toxins that kill Escherichia coli and other closely related species. The mode of action of colicins involves binding to an outer membrane receptor and translocation across the cell envelope, leading to cytotoxicity through specific targets. The mechanism of colicin cytotoxicity includes a non-specific endonuclease activity or depolarization of the cytoplasmic membrane by pore-forming activity. For Group A colicins, translocation requires an interaction between the N-terminal domain of the colicin and a series of membrane- bound and periplasmic proteins known as the Tol system (TolB, TolR, TolA, TolQ, and Pal and the active domain must be translocated through the outer membranes. Protein-protein interactions are intrinsic to virtually every cellular process. The transient protein-protein interactions of the colicin include the interaction with much more complicated assemblies during colicin translocation across the cellular membrane to its target. The potassium release assay detects variation in the K+ content of bacterial cells (K+in). This assays is used to measure the effect of pore-forming colicins such as ColA on an indicator organism by measuring the changes of the K+ concentration in the external medium (K+out ) that are caused by cell killing with a K+ selective electrode. One of the goals of this work is to employ a quantifiable in-vivo method to spot which Tol protein are more implicated in the interaction with colicin A as it is translocated to its target. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=K%2B%20efflux" title="K+ efflux">K+ efflux</a>, <a href="https://publications.waset.org/abstracts/search?q=Colicin%20A" title=" Colicin A"> Colicin A</a>, <a href="https://publications.waset.org/abstracts/search?q=Tol-proteins" title=" Tol-proteins"> Tol-proteins</a>, <a href="https://publications.waset.org/abstracts/search?q=E.%20coli" title=" E. coli"> E. coli</a> </p> <a href="https://publications.waset.org/abstracts/14701/quantifying-the-protein-protein-interaction-between-the-ion-channel-forming-colicin-a-and-the-tol-proteins-by-potassium-efflux-in-e-coli-cells" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/14701.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">409</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4142</span> Region-Specific Secretory Protein, α2M, in Male Reproductive Tract of the Blue Crab And Its Dynamics during Sperm transit towards Female Spermatheca</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Thanyaporn%20Senarai">Thanyaporn Senarai</a>, <a href="https://publications.waset.org/abstracts/search?q=Rapeepun%20Vanichviriyakit"> Rapeepun Vanichviriyakit</a>, <a href="https://publications.waset.org/abstracts/search?q=Shinji%20Miyata"> Shinji Miyata</a>, <a href="https://publications.waset.org/abstracts/search?q=Chihiro%20Sato"> Chihiro Sato</a>, <a href="https://publications.waset.org/abstracts/search?q=Prapee%20Sretarugsa"> Prapee Sretarugsa</a>, <a href="https://publications.waset.org/abstracts/search?q=Wattana%20Weerachatyanukul"> Wattana Weerachatyanukul</a>, <a href="https://publications.waset.org/abstracts/search?q=Ken%20Kitajima"> Ken Kitajima</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, we characterized a region-specific 250 kDa protein that was secreted of MSD fluid, which is believed to play dual functions in forming a spermatophoric wall for sperm physical protection, and in sperm membrane modification as part of sperm maturation process. The partial amino acid sequence and N-terminal sequencing revealed that the MSD-specific 250 kDa protein showed a high similarity with a plasma-rich protein, α-2 macroglobulin (α2M), so termed pp-α2M. This protein was a large glycoprotein contained predominantly mannose and GlcNAc. The expression of pp-α2M mRNA was detected in spermatic duct (SD), androgenic gland (AG) and hematopoietic tissue, while the protein expression was rather specific to the apical cytoplasm of MSD epithelium. The secretory pp-α2M in MSD fluid was acquired onto the MSD sperm membrane and was also found within the matrix of the acrosome. Distally, pp-α2M was removed from spermathecal sperm membrane, while its level kept constant in the sperm AC. Together the results indicate that pp-α2M is a 250 kDa region-specific secretory protein which plays roles in sperm physical protection and also acts as maturation factor in the P. pelagicus sperm. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alpha-2%20macroglobulin" title="alpha-2 macroglobulin">alpha-2 macroglobulin</a>, <a href="https://publications.waset.org/abstracts/search?q=blue%20swimming%20crab" title=" blue swimming crab"> blue swimming crab</a>, <a href="https://publications.waset.org/abstracts/search?q=sperm%20maturation" title=" sperm maturation"> sperm maturation</a>, <a href="https://publications.waset.org/abstracts/search?q=spermatic%20duct" title=" spermatic duct "> spermatic duct </a> </p> <a href="https://publications.waset.org/abstracts/60090/region-specific-secretory-protein-a2m-in-male-reproductive-tract-of-the-blue-crab-and-its-dynamics-during-sperm-transit-towards-female-spermatheca" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/60090.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">329</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4141</span> Development of Numerical Method for Mass Transfer across the Moving Membrane with Selective Permeability: Approximation of the Membrane Shape by Level Set Method for Numerical Integral</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Suguru%20Miyauchi">Suguru Miyauchi</a>, <a href="https://publications.waset.org/abstracts/search?q=Toshiyuki%20Hayase"> Toshiyuki Hayase</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Biological membranes have selective permeability, and the capsules or cells enclosed by the membrane show the deformation by the osmotic flow. This mass transport phenomenon is observed everywhere in a living body. For the understanding of the mass transfer in a body, it is necessary to consider the mass transfer phenomenon across the membrane as well as the deformation of the membrane by a flow. To our knowledge, in the numerical analysis, the method for mass transfer across the moving membrane has not been established due to the difficulty of the treating of the mass flux permeating through the moving membrane with selective permeability. In the existing methods for the mass transfer across the membrane, the approximate delta function is used to communicate the quantities on the interface. The methods can reproduce the permeation of the solute, but cannot reproduce the non-permeation. Moreover, the computational accuracy decreases with decreasing of the permeable coefficient of the membrane. This study aims to develop the numerical method capable of treating three-dimensional problems of mass transfer across the moving flexible membrane. One of the authors developed the numerical method with high accuracy based on the finite element method. This method can capture the discontinuity on the membrane sharply due to the consideration of the jumps in concentration and concentration gradient in the finite element discretization. The formulation of the method takes into account the membrane movement, and both permeable and non-permeable membranes can be treated. However, searching the cross points of the membrane and fluid element boundaries and splitting the fluid element into sub-elements are needed for the numerical integral. Therefore, cumbersome operation is required for a three-dimensional problem. In this paper, we proposed an improved method to avoid the search and split operations, and confirmed its effectiveness. The membrane shape was treated implicitly by introducing the level set function. As the construction of the level set function, the membrane shape in one fluid element was expressed by the shape function of the finite element method. By the numerical experiment, it was found that the shape function with third order appropriately reproduces the membrane shapes. The same level of accuracy compared with the previous method using search and split operations was achieved by using a number of sampling points of the numerical integral. The effectiveness of the method was confirmed by solving several model problems. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=finite%20element%20method" title="finite element method">finite element method</a>, <a href="https://publications.waset.org/abstracts/search?q=level%20set%20method" title=" level set method"> level set method</a>, <a href="https://publications.waset.org/abstracts/search?q=mass%20transfer" title=" mass transfer"> mass transfer</a>, <a href="https://publications.waset.org/abstracts/search?q=membrane%20permeability" title=" membrane permeability"> membrane permeability</a> </p> <a href="https://publications.waset.org/abstracts/57272/development-of-numerical-method-for-mass-transfer-across-the-moving-membrane-with-selective-permeability-approximation-of-the-membrane-shape-by-level-set-method-for-numerical-integral" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/57272.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">250</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4140</span> Computational Prediction of the Effect of S477N Mutation on the RBD Binding Affinity and Structural Characteristic, A Molecular Dynamics Study</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohammad%20Hossein%20Modarressi">Mohammad Hossein Modarressi</a>, <a href="https://publications.waset.org/abstracts/search?q=Mozhgan%20Mondeali"> Mozhgan Mondeali</a>, <a href="https://publications.waset.org/abstracts/search?q=Khabat%20Barkhordari"> Khabat Barkhordari</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20Etemadi"> Ali Etemadi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The COVID-19 pandemic, caused by SARS-CoV-2, has led to significant concerns worldwide due to its catastrophic effects on public health. The SARS-CoV-2 infection is initiated with the binding of the receptor-binding domain (RBD) in its spike protein to the ACE2 receptor in the host cell membrane. Due to the error-prone entity of the viral RNA-dependent polymerase complex, the virus genome, including the coding region for the RBD, acquires new mutations, leading to the appearance of multiple variants. These variants can potentially impact transmission, virulence, antigenicity and evasive immune properties. S477N mutation located in the RBD has been observed in the SARS-CoV-2 omicron (B.1.1. 529) variant. In this study, we investigated the consequences of S477N mutation at the molecular level using computational approaches such as molecular dynamics simulation, protein-protein interaction analysis, immunoinformatics and free energy computation. We showed that displacement of Ser with Asn increases the stability of the spike protein and its affinity to ACE2 and thus increases the transmission potential of the virus. This mutation changes the folding and secondary structure of the spike protein. Also, it reduces antibody neutralization, raising concern about re-infection, vaccine breakthrough and therapeutic values. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=S477N" title="S477N">S477N</a>, <a href="https://publications.waset.org/abstracts/search?q=COVID-19" title=" COVID-19"> COVID-19</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20dynamic" title=" molecular dynamic"> molecular dynamic</a>, <a href="https://publications.waset.org/abstracts/search?q=SARS-COV2%20mutations" title=" SARS-COV2 mutations"> SARS-COV2 mutations</a> </p> <a href="https://publications.waset.org/abstracts/145533/computational-prediction-of-the-effect-of-s477n-mutation-on-the-rbd-binding-affinity-and-structural-characteristic-a-molecular-dynamics-study" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/145533.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">176</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4139</span> Folding of β-Structures via the Polarized Structure-Specific Backbone Charge (PSBC) Model</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yew%20Mun%20Yip">Yew Mun Yip</a>, <a href="https://publications.waset.org/abstracts/search?q=Dawei%20Zhang"> Dawei Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Proteins are the biological machinery that executes specific vital functions in every cell of the human body by folding into their 3D structures. When a protein misfolds from its native structure, the machinery will malfunction and lead to misfolding diseases. Although in vitro experiments are able to conclude that the mutations of the amino acid sequence lead to incorrectly folded protein structures, these experiments are unable to decipher the folding process. Therefore, molecular dynamic (MD) simulations are employed to simulate the folding process so that our improved understanding of the folding process will enable us to contemplate better treatments for misfolding diseases. MD simulations make use of force fields to simulate the folding process of peptides. Secondary structures are formed via the hydrogen bonds formed between the backbone atoms (C, O, N, H). It is important that the hydrogen bond energy computed during the MD simulation is accurate in order to direct the folding process to the native structure. Since the atoms involved in a hydrogen bond possess very dissimilar electronegativities, the more electronegative atom will attract greater electron density from the less electronegative atom towards itself. This is known as the polarization effect. Since the polarization effect changes the electron density of the two atoms in close proximity, the atomic charges of the two atoms should also vary based on the strength of the polarization effect. However, the fixed atomic charge scheme in force fields does not account for the polarization effect. In this study, we introduce the polarized structure-specific backbone charge (PSBC) model. The PSBC model accounts for the polarization effect in MD simulation by updating the atomic charges of the backbone hydrogen bond atoms according to equations derived between the amount of charge transferred to the atom and the length of the hydrogen bond, which are calculated from quantum-mechanical calculations. Compared to other polarizable models, the PSBC model does not require quantum-mechanical calculations of the peptide simulated at every time-step of the simulation and maintains the dynamic update of atomic charges, thereby reducing the computational cost and time while accounting for the polarization effect dynamically at the same time. The PSBC model is applied to two different β-peptides, namely the Beta3s/GS peptide, a de novo designed three-stranded β-sheet whose structure is folded in vitro and studied by NMR, and the trpzip peptides, a double-stranded β-sheet where a correlation is found between the type of amino acids that constitute the β-turn and the β-propensity. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hydrogen%20bond" title="hydrogen bond">hydrogen bond</a>, <a href="https://publications.waset.org/abstracts/search?q=polarization%20effect" title=" polarization effect"> polarization effect</a>, <a href="https://publications.waset.org/abstracts/search?q=protein%20folding" title=" protein folding"> protein folding</a>, <a href="https://publications.waset.org/abstracts/search?q=PSBC" title=" PSBC"> PSBC</a> </p> <a href="https://publications.waset.org/abstracts/45837/folding-of-v-structures-via-the-polarized-structure-specific-backbone-charge-psbc-model" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/45837.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">270</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4138</span> Protein Tertiary Structure Prediction by a Multiobjective Optimization and Neural Network Approach</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Alexandre%20Barbosa%20de%20Almeida">Alexandre Barbosa de Almeida</a>, <a href="https://publications.waset.org/abstracts/search?q=Telma%20Woerle%20de%20Lima%20Soares"> Telma Woerle de Lima Soares</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Protein structure prediction is a challenging task in the bioinformatics field. The biological function of all proteins majorly relies on the shape of their three-dimensional conformational structure, but less than 1% of all known proteins in the world have their structure solved. This work proposes a deep learning model to address this problem, attempting to predict some aspects of the protein conformations. Throughout a process of multiobjective dominance, a recurrent neural network was trained to abstract the particular bias of each individual multiobjective algorithm, generating a heuristic that could be useful to predict some of the relevant aspects of the three-dimensional conformation process formation, known as protein folding. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ab%20initio%20heuristic%20modeling" title="Ab initio heuristic modeling">Ab initio heuristic modeling</a>, <a href="https://publications.waset.org/abstracts/search?q=multiobjective%20optimization" title=" multiobjective optimization"> multiobjective optimization</a>, <a href="https://publications.waset.org/abstracts/search?q=protein%20structure%20prediction" title=" protein structure prediction"> protein structure prediction</a>, <a href="https://publications.waset.org/abstracts/search?q=recurrent%20neural%20network" title=" recurrent neural network"> recurrent neural network</a> </p> <a href="https://publications.waset.org/abstracts/141565/protein-tertiary-structure-prediction-by-a-multiobjective-optimization-and-neural-network-approach" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/141565.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">205</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4137</span> Recovery of Proteins from EDAM Whey Using Membrane Ultrafiltration</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=F.%20Yelles-Allam">F. Yelles-Allam</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20A.%20Nouani"> A. A. Nouani</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In Algeria, whey is discarded without any treatment and this causes not only pollution problem, but also a loss in nutritive components of milk. In this paper, characterization of EDAM whey, which is resulted from pasteurised mixture of cow’s milk and skim milk, and recovery of whey protein by ultrafiltration / diafiltration, was studied. The physical-chemical analysis of whey has emphasized on its pollutant and nutritive characteristics. In fact, its DBO5 and DCO are 49.33, and 127.71 gr of O2/l of whey respectively. It contains: fat (1,90±0,1 gr/l), lactose (47.32±1,57 gr/l), proteins (8.04±0,2 gr/l) and ashes (5,20±0,15 gr/l), calcium (0,48±0,04 gr/l), Na (1.104gr/l), K (1.014 gr/l), Mg (0.118 gr/l) and P (0.482 gr/l). Ultrafiltration was carried out in a polyetersulfone membrane with a cut-off of 10K. Its hydraulic intrinsic resistance and permeability are respectively: 2.041.1012 m-1 and 176,32 l/h.m2 at PTM of 1 bar. The retentate obtained at FC6, contains 16,33g/l of proteins and 70,25 g/l of dry matter. The retention rate of protein is 97, 7% and the decrease in DBO5 and DCO are at 18.875 g /l and 42.818 g/l respectively. Diafiltration performed on protein concentrates allowed the complete removal of lactose and minerals. The ultrafiltration of the whey before the disposal is an alternative for Algéria dairy industry. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=diafiltration" title="diafiltration">diafiltration</a>, <a href="https://publications.waset.org/abstracts/search?q=DBO" title=" DBO"> DBO</a>, <a href="https://publications.waset.org/abstracts/search?q=DCO" title=" DCO"> DCO</a>, <a href="https://publications.waset.org/abstracts/search?q=protein" title=" protein"> protein</a>, <a href="https://publications.waset.org/abstracts/search?q=ultrafiltration" title=" ultrafiltration"> ultrafiltration</a>, <a href="https://publications.waset.org/abstracts/search?q=whey" title=" whey"> whey</a> </p> <a href="https://publications.waset.org/abstracts/46499/recovery-of-proteins-from-edam-whey-using-membrane-ultrafiltration" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46499.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">256</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4136</span> Protein and MDA (Malondialdehyde) Profil of Bull Sperm and Seminal Plasma After Freezing</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sri%20Rahayu">Sri Rahayu</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Dwi%20Susan"> M. Dwi Susan</a>, <a href="https://publications.waset.org/abstracts/search?q=Aris%20Soewondo"> Aris Soewondo</a>, <a href="https://publications.waset.org/abstracts/search?q=W.%20M.%20Agung%20Pramana"> W. M. Agung Pramana</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Semen is an organic fluid (seminal plasma) that contain spermatozoa. Proteins are one of the major seminal plasma components that modulate sperm functionality, influence sperm capacitation and maintaining the stability of the membrane. Semen freezing is a procedure to preserve sperm cells. The process causes decrease in sperm viability due to temperature shock and oxidation stress. Oxidation stress is a disturbance on phosphorylation that increases ROS concentration, and it produces lipid peroxide in spermatozoa membrane resulted in high MDA (malondialdehyde) concentration. The objective of this study was to examine the effect of freezing on protein and MDA profile of bovine sperm cell and seminal plasma after freezing. Protein and MDA of sperm cell and seminal plasma were isolated from 10 sample. Protein profiles was analyzed by SDS PAGE with separating gel 12,5 %. The concentration of MDA was measured by spectrophotometer. The results of the research indicated that freezing of semen cause lost of the seminal plasma proteins with molecular with 20, 10, and 9 kDa. In addition, the result research showed that protein of the sperm (26, 10, 9, 7, and 6 kDa) had been lost. There were difference MDA concentration of seminal plasma and sperm cell were increase after freezing. MDA concentration of seminal plasma before and after freezing were 2.2 and 2.4 nmol, respectively. MDA concentration of sperm cell before and after freezing were 1,5 and 1.8 nmol, respectively. In conclusion, there were differences protein profiles of spermatozoa before and after semen freezing and freezing cause increasing of the MDA concentration. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=MDA" title="MDA">MDA</a>, <a href="https://publications.waset.org/abstracts/search?q=semen%20freezing" title=" semen freezing"> semen freezing</a>, <a href="https://publications.waset.org/abstracts/search?q=SDS%20PAGE" title=" SDS PAGE"> SDS PAGE</a>, <a href="https://publications.waset.org/abstracts/search?q=protein%20profile" title=" protein profile"> protein profile</a> </p> <a href="https://publications.waset.org/abstracts/9455/protein-and-mda-malondialdehyde-profil-of-bull-sperm-and-seminal-plasma-after-freezing" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/9455.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">275</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4135</span> The UbiB Family Member Cqd1 Forms a Membrane Contact Site in Mitochondria</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=S.%20Khosravi">S. Khosravi</a>, <a href="https://publications.waset.org/abstracts/search?q=X.%20Chelius"> X. Chelius</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Unger"> A. Unger</a>, <a href="https://publications.waset.org/abstracts/search?q=D.%20Rieger"> D. Rieger</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20Frickel"> J. Frickel</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Sachsenheimer"> T. Sachsenheimer</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Luechtenborg"> C. Luechtenborg</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20Schieweck"> R. Schieweck</a>, <a href="https://publications.waset.org/abstracts/search?q=B.%20Bruegger"> B. Bruegger</a>, <a href="https://publications.waset.org/abstracts/search?q=B.%20Westermann"> B. Westermann</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Klecker"> T. Klecker</a>, <a href="https://publications.waset.org/abstracts/search?q=W.%20Neupert"> W. Neupert</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20E.%20Harner"> M. E. Harner</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The use of Saccharomyces cerevisiae as a model organism to study eukaryotic cell functions has been used successfully for decades. Like virtually all eukaryotic cells, they contain mitochondria as essential organelles performing various functions, including participation in lipid metabolism. They are separated from the cytosol by a double membrane system consisting of the mitochondrial inner membrane (MIM) and the mitochondrial outer membrane (MOM). This physical separation of the mitochondria requires an exchange of metabolites, proteins, and lipids. Proteinaceous contact sites are thought to be important for this communication. Recently, it was found that Cqd1, in cooperation with Cqd2, controls the distribution of Coenzyme Q within the cell. In this study, a contact site is described, formed by the MOM protein complex Por1-Om14 and the UbiB protein kinase-like MIM protein Cqd1. The present results suggest the additional involvement of Cqd1 in the homeostasis of phospholipids. Moreover, we show that overexpression of the UbiB family proteins also causes tethering of the mitochondria to the endoplasmatic reticulum. Due to the conservation of the subunits of this contact site to higher eukaryotes, its identification in S. cerevisiae might provide promising avenues for further research in other organisms. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=contact%20sites" title="contact sites">contact sites</a>, <a href="https://publications.waset.org/abstracts/search?q=mitochondrial%20architecture" title=" mitochondrial architecture"> mitochondrial architecture</a>, <a href="https://publications.waset.org/abstracts/search?q=mitochondrial%20proteins" title=" mitochondrial proteins"> mitochondrial proteins</a>, <a href="https://publications.waset.org/abstracts/search?q=yeast%20mitochondria" title=" yeast mitochondria"> yeast mitochondria</a> </p> <a href="https://publications.waset.org/abstracts/163034/the-ubib-family-member-cqd1-forms-a-membrane-contact-site-in-mitochondria" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/163034.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">106</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4134</span> AFM Probe Sensor Designed for Cellular Membrane Components</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sarmiza%20Stanca">Sarmiza Stanca</a>, <a href="https://publications.waset.org/abstracts/search?q=Wolfgang%20Fritzsche"> Wolfgang Fritzsche</a>, <a href="https://publications.waset.org/abstracts/search?q=Christoph%20%20Krafft"> Christoph Krafft</a>, <a href="https://publications.waset.org/abstracts/search?q=J%C3%BCrgen%20Popp"> Jürgen Popp</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Independent of the cell type a thin layer of a few nanometers thickness surrounds the cell interior as the cellular membrane. The transport of ions and molecules through the membrane is achieved in a very precise way by pores. Understanding the process of opening and closing the pores due to an electrochemical gradient across the membrane requires knowledge of the pore constitutive proteins. Recent reports prove the access to the molecular level of the cellular membrane by atomic force microscopy (AFM). This technique also permits an electrochemical study in the immediate vicinity of the tip. Specific molecules can be electrochemically localized in the natural cellular membrane. Our work aims to recognize the protein domains of the pores using an AFM probe as a miniaturized amperometric sensor, and to follow the protein behavior while changing the applied potential. The intensity of the current produced between the surface and the AFM probe is amplified and detected simultaneously with the surface imaging. The AFM probe plays the role of the working electrode and the substrate, a conductive glass on which the cells are grown, represent the counter electrode. For a better control of the electric potential on the probe, a third electrode Ag/AgCl wire is mounted in the circuit as a reference electrode. The working potential is applied between the electrodes with a programmable source and the current intensity in the circuit is recorded with a multimeter. The applied potential considers the overpotential at the electrode surface and the potential drop due to the current flow through the system. The reported method permits a high resolved electrochemical study of the protein domains on the living cell membrane. The amperometric map identifies areas of different current intensities on the pore depending on the applied potential. The reproducibility of this method is limited by the tip shape, the uncontrollable capacitance, which occurs at the apex and a potential local charge separation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=AFM" title="AFM">AFM</a>, <a href="https://publications.waset.org/abstracts/search?q=sensor" title=" sensor"> sensor</a>, <a href="https://publications.waset.org/abstracts/search?q=membrane" title=" membrane"> membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=pores" title=" pores"> pores</a>, <a href="https://publications.waset.org/abstracts/search?q=proteins" title=" proteins"> proteins</a> </p> <a href="https://publications.waset.org/abstracts/29017/afm-probe-sensor-designed-for-cellular-membrane-components" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/29017.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">307</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4133</span> Towards the Inhibition Mechanism of Lysozyme Fibrillation by Hydrogen Sulfide</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Indra%20Gonzalez%20Ojeda">Indra Gonzalez Ojeda</a>, <a href="https://publications.waset.org/abstracts/search?q=Tatiana%20Quinones"> Tatiana Quinones</a>, <a href="https://publications.waset.org/abstracts/search?q=Manuel%20Rosario"> Manuel Rosario</a>, <a href="https://publications.waset.org/abstracts/search?q=Igor%20Lednev"> Igor Lednev</a>, <a href="https://publications.waset.org/abstracts/search?q=Juan%20Lopez%20Garriga"> Juan Lopez Garriga</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Amyloid fibrils are stable aggregates of misfolded protein associated with many neurodegenerative disorders. It has been shown that hydrogen sulfide (H2S), inhibits the fibrillation of lysozyme through the formation of trisulfide (S-S-S) bonds. However, the overall mechanism remains elusive. Here, the concentration dependence of H2S effect was investigated using Atomic force microscopy (AFM), non-resonance Raman spectroscopy, Deep-UV Raman spectroscopy and circular dichroism (CD). It was found that small spherical aggregates with trisulfide bonds and a unique secondary structure were formed instead of amyloid fibrils when adding concentrations of 25 mM and 50 mM of H2S. This could indicate that H2S might serve as a protecting agent for the protein. However, further characterization of these aggregates and their trisulfide bonds is needed to fully unravel the function H2S has on protein fibrillation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=amyloid%20fibrils" title="amyloid fibrils">amyloid fibrils</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrogen%20sulfide" title=" hydrogen sulfide"> hydrogen sulfide</a>, <a href="https://publications.waset.org/abstracts/search?q=protein%20folding" title=" protein folding"> protein folding</a>, <a href="https://publications.waset.org/abstracts/search?q=raman%20spectroscopy" title=" raman spectroscopy"> raman spectroscopy</a> </p> <a href="https://publications.waset.org/abstracts/86031/towards-the-inhibition-mechanism-of-lysozyme-fibrillation-by-hydrogen-sulfide" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/86031.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">216</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4132</span> Kinetics of Cu(II) Transport through Bulk Liquid Membrane with Different Membrane Materials</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Siu%20Hua%20Chang">Siu Hua Chang</a>, <a href="https://publications.waset.org/abstracts/search?q=Ayub%20Md%20Som"> Ayub Md Som</a>, <a href="https://publications.waset.org/abstracts/search?q=Jagannathan%20Krishnan"> Jagannathan Krishnan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The kinetics of Cu(II) transport through a bulk liquid membrane with different membrane materials was investigated in this work. Three types of membrane materials were used: Fresh cooking oil, waste cooking oil, and kerosene each of which was mixed with di-2-ethylhexylphosphoric acid (carrier) and tributylphosphate (modifier). Kinetic models derived from the kinetic laws of two consecutive irreversible first-order reactions were used to study the facilitated transport of Cu(II) across the source, membrane, and receiving phases of bulk liquid membrane. It was found that the transport kinetics of Cu(II) across the source phase was not affected by different types of membrane materials but decreased considerably when the membrane materials changed from kerosene, waste cooking oil to fresh cooking oil. The rate constants of Cu(II) removal and recovery processes through the bulk liquid membrane were also determined. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=transport%20kinetics" title="transport kinetics">transport kinetics</a>, <a href="https://publications.waset.org/abstracts/search?q=Cu%28II%29" title=" Cu(II)"> Cu(II)</a>, <a href="https://publications.waset.org/abstracts/search?q=bulk%20liquid%20membrane" title=" bulk liquid membrane"> bulk liquid membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=waste%20cooking%20oil" title=" waste cooking oil "> waste cooking oil </a> </p> <a href="https://publications.waset.org/abstracts/2082/kinetics-of-cuii-transport-through-bulk-liquid-membrane-with-different-membrane-materials" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/2082.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">426</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4131</span> CAP-Glycine Protein Governs Growth, Differentiation, and the Pathogenicity of Global Meningoencephalitis Fungi</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kyung-Tae%20Lee">Kyung-Tae Lee</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20Li%20Wang"> Li Li Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Kwang-Woo%20Jung"> Kwang-Woo Jung</a>, <a href="https://publications.waset.org/abstracts/search?q=Yong-Sun%20Bahn"> Yong-Sun Bahn</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Microtubules are involved in mechanical support, cytoplasmic organization as well as in a number of cellular processes by interacting with diverse microtubule-associated proteins (MAPs), such as plus-end tracking proteins, motor proteins, and tubulin-folding cofactors. A common feature of these proteins is the presence of a cytoskeleton-associated protein-glycine-rich (CAP-Gly) domain, which is evolutionarily conserved and generally considered to bind to α-tubulin to regulate functions of microtubules. However, there has been a dearth of research on CAP-Gly proteins in fungal pathogens, including Cryptococcus neoformans, which causes fatal meningoencephalitis globally. In this study, we identified five CAP-Gly proteins encoding genes in C. neoformans. Among these, Cgp1, encoded by CNAG_06352, has a unique domain structure that has not been reported before in other eukaryotes. Supporting the role of Cpg1 in microtubule-related functions, we demonstrate that deletion or overexpression of CGP1 alters cellular susceptibility to thiabendazole, a microtubule destabilizer, and Cgp1 is co-localized with cytoplasmic microtubules. Related to the cellular functions of microtubules, Cgp1 also governs maintenance of membrane stability and genotoxic stress responses. Furthermore, we demonstrate that Cgp1 uniquely regulates sexual differentiation of C. neoformans with distinct roles in the early and late stage of mating. Our domain analysis reveals that the CAP-Gly domain plays major roles in all the functions of Cgp1. Finally, the cgp1Δ mutant is attenuated in virulence. In conclusion, this novel CAP-Gly protein, Cgp1, has pleotropic roles in regulating growth, stress responses, differentiation and pathogenicity of C. neoformans. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=human%20fungal%20pathogen" title="human fungal pathogen">human fungal pathogen</a>, <a href="https://publications.waset.org/abstracts/search?q=CAP-Glycine%20protein" title=" CAP-Glycine protein"> CAP-Glycine protein</a>, <a href="https://publications.waset.org/abstracts/search?q=microtubule" title=" microtubule"> microtubule</a>, <a href="https://publications.waset.org/abstracts/search?q=meningoencephalitis" title=" meningoencephalitis"> meningoencephalitis</a> </p> <a href="https://publications.waset.org/abstracts/63213/cap-glycine-protein-governs-growth-differentiation-and-the-pathogenicity-of-global-meningoencephalitis-fungi" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/63213.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">315</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4130</span> Study of a Developed Model Describing a Vacuum Membrane Distillation Unit Coupled to Solar Energy </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fatma%20Khaled">Fatma Khaled</a>, <a href="https://publications.waset.org/abstracts/search?q=Khaoula%20Hidouri"> Khaoula Hidouri</a>, <a href="https://publications.waset.org/abstracts/search?q=Bechir%20Chaouachi"> Bechir Chaouachi </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Desalination using solar energy coupled with membrane techniques such as vacuum membrane distillation (VMD) is considered as an interesting alternative for the production of pure water. During this work, a developed model of a polytetrafluoroethylene (PTFE) hollow fiber membrane module of a VMD unit of seawater was carried out. This simulation leads to establishing a comparison between the effects of two different equations of the vaporization latent heat on the membrane surface temperature and on the unit productivity. Besides, in order to study the effect of putting membrane modules in series on the outlet fluid temperature and on the productivity of the process, a simulation was executed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=vacuum%20membrane%20distillation" title="vacuum membrane distillation">vacuum membrane distillation</a>, <a href="https://publications.waset.org/abstracts/search?q=membrane%20module" title=" membrane module"> membrane module</a>, <a href="https://publications.waset.org/abstracts/search?q=membrane%20temperature" title=" membrane temperature"> membrane temperature</a>, <a href="https://publications.waset.org/abstracts/search?q=productivity" title=" productivity"> productivity</a> </p> <a href="https://publications.waset.org/abstracts/107225/study-of-a-developed-model-describing-a-vacuum-membrane-distillation-unit-coupled-to-solar-energy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/107225.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">191</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4129</span> On Fourier Type Integral Transform for a Class of Generalized Quotients</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20S.%20Issa">A. S. Issa</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20K.%20Q.%20AL-Omari"> S. K. Q. AL-Omari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this paper, we investigate certain spaces of generalized functions for the Fourier and Fourier type integral transforms. We discuss convolution theorems and establish certain spaces of distributions for the considered integrals. The new Fourier type integral is well-defined, linear, one-to-one and continuous with respect to certain types of convergences. Many properties and an inverse problem are also discussed in some details. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Boehmian" title="Boehmian">Boehmian</a>, <a href="https://publications.waset.org/abstracts/search?q=Fourier%20integral" title=" Fourier integral"> Fourier integral</a>, <a href="https://publications.waset.org/abstracts/search?q=Fourier%20type%20integral" title=" Fourier type integral"> Fourier type integral</a>, <a href="https://publications.waset.org/abstracts/search?q=generalized%20quotient" title=" generalized quotient"> generalized quotient</a> </p> <a href="https://publications.waset.org/abstracts/45947/on-fourier-type-integral-transform-for-a-class-of-generalized-quotients" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/45947.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">365</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4128</span> Basic Evaluation for Polyetherimide Membrane Using Spectroscopy Techniques </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hanan%20Alenezi">Hanan Alenezi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Membrane performance depends on the kind of solvent used in preparation. A membrane made by Polyetherimide (PEI) was evaluated for gas separation using X-Ray Diffraction (XRD), Scanning electron microscope (SEM), and Energy Dispersive X-Ray Spectroscopy (EDS). The purity and the thickness are detected to evaluate the membrane in order to optimize PEI membrane preparation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Energy%20Dispersive%20X-Ray%20Spectroscopy%20%28EDS%29" title="Energy Dispersive X-Ray Spectroscopy (EDS)">Energy Dispersive X-Ray Spectroscopy (EDS)</a>, <a href="https://publications.waset.org/abstracts/search?q=Membrane" title=" Membrane"> Membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=Polyetherimide%20PEI" title=" Polyetherimide PEI"> Polyetherimide PEI</a>, <a href="https://publications.waset.org/abstracts/search?q=Scanning%20electron%20microscope%20%28SEM%29" title=" Scanning electron microscope (SEM)"> Scanning electron microscope (SEM)</a>, <a href="https://publications.waset.org/abstracts/search?q=Solvent" title=" Solvent"> Solvent</a>, <a href="https://publications.waset.org/abstracts/search?q=X-Ray%20Diffraction%20%28XRD%29" title=" X-Ray Diffraction (XRD)"> X-Ray Diffraction (XRD)</a> </p> <a href="https://publications.waset.org/abstracts/120499/basic-evaluation-for-polyetherimide-membrane-using-spectroscopy-techniques" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/120499.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">183</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4127</span> Cellular Degradation Activity is Activated by Ambient Temperature Reduction in an Annual Fish (Nothobranchius rachovii)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Cheng-Yen%20Lu">Cheng-Yen Lu</a>, <a href="https://publications.waset.org/abstracts/search?q=Chin-Yuan%20Hsu"> Chin-Yuan Hsu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ambient temperature reduction (ATR) can extend the lifespan of an annual fish (Nothobranchius rachovii), but the underlying mechanism is unknown. In this study, the expression, concentration, and activity of cellular-degraded molecules were evaluated in the muscle of N. rachovii reared under high (30 °C), moderate (25 °C), and low (20 °C) ambient temperatures by biochemical techniques. The results showed that (i) the activity of the 20S proteasome, the expression of microtubule-associated protein 1 light chain 3-II (LC3-II), the expression of lysosome-associated membrane protein type 2a (Lamp 2a), and lysosome activity increased with ATR; (ii) the expression of the 70 kD heat shock cognate protein (Hsc 70) decreased with ATR; (iii) the expression of the 20S proteasome, the expression of lysosome-associated membrane protein type 1 (Lamp 1), the expression of molecular target of rapamycin (mTOR), the expression of phosphorylated mTOR (p-mTOR), and the p-mTOR/mTOR ratio did not change with ATR. These findings indicated that ATR activated the activity of proteasome, macroautophagy, and chaperone-mediated autophagy. Taken together these data reveal that ATR likely activates cellular degradation activity to extend the lifespan of N. rachovii. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ambient%20temperature%20reduction" title="ambient temperature reduction">ambient temperature reduction</a>, <a href="https://publications.waset.org/abstracts/search?q=autophagy" title=" autophagy"> autophagy</a>, <a href="https://publications.waset.org/abstracts/search?q=degradation%20activity" title=" degradation activity"> degradation activity</a>, <a href="https://publications.waset.org/abstracts/search?q=lifespan" title=" lifespan"> lifespan</a>, <a href="https://publications.waset.org/abstracts/search?q=proteasome" title=" proteasome"> proteasome</a> </p> <a href="https://publications.waset.org/abstracts/23211/cellular-degradation-activity-is-activated-by-ambient-temperature-reduction-in-an-annual-fish-nothobranchius-rachovii" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/23211.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">459</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4126</span> Improved 3D Structure Prediction of Beta-Barrel Membrane Proteins by Using Evolutionary Coupling Constraints, Reduced State Space and an Empirical Potential Function</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wei%20Tian">Wei Tian</a>, <a href="https://publications.waset.org/abstracts/search?q=Jie%20Liang"> Jie Liang</a>, <a href="https://publications.waset.org/abstracts/search?q=Hammad%20Naveed"> Hammad Naveed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Beta-barrel membrane proteins are found in the outer membrane of gram-negative bacteria, mitochondria, and chloroplasts. They carry out diverse biological functions, including pore formation, membrane anchoring, enzyme activity, and bacterial virulence. In addition, beta-barrel membrane proteins increasingly serve as scaffolds for bacterial surface display and nanopore-based DNA sequencing. Due to difficulties in experimental structure determination, they are sparsely represented in the protein structure databank and computational methods can help to understand their biophysical principles. We have developed a novel computational method to predict the 3D structure of beta-barrel membrane proteins using evolutionary coupling (EC) constraints and a reduced state space. Combined with an empirical potential function, we can successfully predict strand register at > 80% accuracy for a set of 49 non-homologous proteins with known structures. This is a significant improvement from previous results using EC alone (44%) and using empirical potential function alone (73%). Our method is general and can be applied to genome-wide structural prediction. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=beta-barrel%20membrane%20proteins" title="beta-barrel membrane proteins">beta-barrel membrane proteins</a>, <a href="https://publications.waset.org/abstracts/search?q=structure%20prediction" title=" structure prediction"> structure prediction</a>, <a href="https://publications.waset.org/abstracts/search?q=evolutionary%20constraints" title=" evolutionary constraints"> evolutionary constraints</a>, <a href="https://publications.waset.org/abstracts/search?q=reduced%20state%20space" title=" reduced state space"> reduced state space</a> </p> <a href="https://publications.waset.org/abstracts/40565/improved-3d-structure-prediction-of-beta-barrel-membrane-proteins-by-using-evolutionary-coupling-constraints-reduced-state-space-and-an-empirical-potential-function" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/40565.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">618</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4125</span> Water Purification By Novel Nanocomposite Membrane</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=E.%20S.%20Johal">E. S. Johal</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20S.%20Saini"> M. S. Saini</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20K.%20Jha"> M. K. Jha</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Currently, 1.1 billion people are at risk due to lack of clean water and about 35 % of people in the developed world die from water related problem. To alleviate these problems water purification technology requires new approaches for effective management and conservation of water resources. Electrospun nanofibres membrane has a potential for water purification due to its high large surface area and good mechanical strength. In the present study PAMAM dendrimers composite nynlon-6 nanofibres membrane was prepared by crosslinking method using Glutaraldehyde. Further, the efficacy of the modified membrane can be renewed by mere exposure of the saturated membrane with the solution having acidic pH. The modified membrane can be used as an effective tool for water purification. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dendrimer" title="dendrimer">dendrimer</a>, <a href="https://publications.waset.org/abstracts/search?q=nanofibers" title=" nanofibers"> nanofibers</a>, <a href="https://publications.waset.org/abstracts/search?q=nanocomposite%20membrane" title=" nanocomposite membrane"> nanocomposite membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=water%20purification" title=" water purification"> water purification</a> </p> <a href="https://publications.waset.org/abstracts/9638/water-purification-by-novel-nanocomposite-membrane" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/9638.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">356</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4124</span> Optical and Double Folding Model Analysis for Alpha Particles Elastically Scattered from 9Be and 11B Nuclei at Different Energies</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ahmed%20H.%20Amer">Ahmed H. Amer</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Amar"> A. Amar</a>, <a href="https://publications.waset.org/abstracts/search?q=Sh.%20Hamada"> Sh. Hamada</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20I.%20Bondouk"> I. I. Bondouk</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20A.%20El-Hussiny"> F. A. El-Hussiny</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Elastic scattering of α-particles from 9Be and 11B nuclei at different alpha energies have been analyzed. Optical model parameters (OMPs) of α-particles elastic scattering by these nuclei at different energies have been obtained. In the present calculations, the real part of the optical potential are derived by folding of nucleon-nucleon (NN) interaction into nuclear matter density distribution of the projectile and target nuclei using computer code FRESCO. A density-dependent version of the M3Y interaction (CDM3Y6), which is based on the G-matrix elements of the Paris NN potential, has been used. Volumetric integrals of the real and imaginary potential depth (JR, JW) have been calculated and found to be energy dependent. Good agreement between the experimental data and the theoretical predictions in the whole angular range. In double folding (DF) calculations, the obtained normalization coeﬃcient Nr is in the range 0.70–1.32. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=elastic%20scattering" title="elastic scattering">elastic scattering</a>, <a href="https://publications.waset.org/abstracts/search?q=optical%20model" title=" optical model"> optical model</a>, <a href="https://publications.waset.org/abstracts/search?q=double%20folding%20model" title=" double folding model"> double folding model</a>, <a href="https://publications.waset.org/abstracts/search?q=density%20distribution" title=" density distribution"> density distribution</a> </p> <a href="https://publications.waset.org/abstracts/45164/optical-and-double-folding-model-analysis-for-alpha-particles-elastically-scattered-from-9be-and-11b-nuclei-at-different-energies" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/45164.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">290</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=integral%20membrane%20protein%20folding&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=integral%20membrane%20protein%20folding&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=integral%20membrane%20protein%20folding&page=4">4</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=integral%20membrane%20protein%20folding&page=5">5</a></li> <li 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