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CreMap™ MHC-Peptide Binding Assay Service - Creative Biolabs

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It contains three major steps: the detection of MHC-peptide binding assays, followed by rate assays and cell assays to validate the high MHC-affinity peptides. Peptides used for this assay can be provided by clients or synthesized by our peptide library platform. </p> <p class="show-center"> <img loading="lazy" src="static/img/CreMap-MHC-Peptide-Binding-Assay.png" width="420" height="320" alt="CreMap™ MHC-Peptide Binding Assay" />Fig 1. The workflow of MHC-Peptide Binding Assay. </p> <p> <strong>Binding assay:</strong> The binding of each peptide with MHC molecules aims to measure the capability of candidate peptides to stabilize the structure of MHC-peptide complex, which is reflected by the distinct signal. Only when the peptides could bind to MHC and stabilize the conformation will the signal be released. Each candidate peptide achieves a score relative to the positive control peptide (known T cell epitope). And based on corresponding analysis of signal percentage, the lead selections will be chosen for the next step study. </p> <p> <strong>Rate assay:</strong> This assay is followed by the MHC-peptide binding assay and targets for quantitative determination of the binding abilities of the selected peptides. Peptides that are presented with enough length have the greater chance to be recognized by T cells. The on-or/and off-rates for the selected peptides are measured at different time points. Comprehensive analysis and achieve a score for the individual peptide. The higher score represents a better T cell epitope candidate. </p> <p> <strong>Validation assay:</strong> The strategies above will cut down the number of candidate epitopes for further research. Then cell assays could be committed to detecting whether these selected peptides have the property to evoke relevant T cell responses. Detection of the T cell responses induced by immunogenic peptides keeps two major approaches: determine the proliferation of T cells or the cytokine-secreting by T cells in the presence of potentially immunogenic peptides. T cell proliferation assays are performed by combining with the MHC multimers (tetramers, Pentamers, dextramers) techniques which are detected by flow cytometer. The cytokine secreting of T cells is committed with the ultrasensitive ELISPOT technique to accurately reflect the antigen-specific T cell responses. </p> <h2 class="h2_tit page_tab_margin" id="tab2"> Key Features </h2> <ul class="ullist"> <li> Rapid and comprehensive T cell epitope mapping technique service for customers with short turnaround time </li> <li> Cost effective to perform a series of complete analysis for customers </li> <li> An optimal choice for immunogenicity analysis of new therapeutic drugs and a new vaccine development </li> </ul> <br /> <p> <strong>Creative Biolabs</strong> has years of experience in offering our customer epitope mapping techniques and we are happy to provide the advanced technical support to help our clients find the T cell epitope. If you are interested in our service, please <a class="inquiry-button">contact us</a> for more information and a detailed quote. </p> <p> Other optional <a href="/CreMap-T-Cell-Epitope-Discovery-Service.html">CreMap™ T cell epitope discovery</a> services: </p> <ul class="ullist"> <li> <a href="/cremap-antigen-processing-assay.html">CreMap™ Antigen Processing Assay</a> </li> </ul> <h2 class="h2_tit page_tab_margin" id="tab3"> Published Data </h2> <ul class="ullist"> <li> <strong>Analysis of CD8+ T-cell Response through MHC-Peptide Binding Assay in Both Cis and Trans Configurations</strong> </li> </ul> <p class="show-center"> <img loading="lazy" src="static/img/1-2-8-3-2-1-mhc-peptide-binding-assay-2.jpg" width="460" height="275" alt="" />Fig. 2 CD8-pMHC binding in cis negatively regulates CD8 coreceptor function.<sup>1,2</sup> </p> <p> The article reveals significant insights into the regulation of CD8+ T-cell responses through the interaction of CD8 with MHC-peptide complexes in both cis and trans configurations, highlighting the role of differential binding in modulating T-cell activation. This is mediated by distinct structural interactions and posttranslational modifications, such as a disulfide bond and O-linked glycosylation, which influence the orientation and binding affinity of CD8. The MHC-peptide binding assay is pivotal, demonstrating the alternate binding orientation of CD8 in cis, showing that this interaction can inhibit T-cell activation. This discovery adds complexity to our understanding of T-cell receptor signaling and opens up new possibilities for therapeutic interventions in immune regulation, with potential applications in enhancing immune responses against pathogens or tumors, or in preventing autoimmune responses. </p> <div class="reference"> <strong>References</strong> <ol class="ollist decimal"> <li> Liu, Yang, et al. "CD8 Binding of MHC-Peptide Complexes in cis or trans Regulates CD8+ T-cell Responses." <em>Journal of molecular biology</em> 431.24 (2019): 4941-4958. </li> <li> under Open Access license <a href="https://creativecommons.org/licenses/by/4.0/">CC BY 4.0</a>, without modification. </li> </ol> </div> <script type="text/javascript"> window.addEventListener('load',function(){ faqlist(4); }); </script> <h2 class="h2_tit page_tab_margin" id="tab4"> FAQ </h2> <ol class="ollist faqlist"> <li> <span class="sFAQTit">What is an MHC-peptide binding assay?</span> <p> The MHC-peptide binding assay is used to determine the affinity and specificity with which peptides bind to Major Histocompatibility Complex (MHC) molecules. This assay is crucial for understanding T-cell recognition and response, which are central to the immune system's ability to recognize and react to pathogens. </p> </li> <li> <span class="sFAQTit">Why is the MHC-peptide binding assay important in immunological research?</span> <p> MHC-peptide binding assays can help identify which peptide fragments of proteins will be presented on the cell surface by MHC molecules, a process essential for T-cell immune response. This is critical for developing vaccines, cancer immunotherapies, and studying autoimmune diseases. </p> </li> <li> <span class="sFAQTit">How does an MHC-peptide binding assay work?</span> <p> The assay typically involves incubating synthetic peptides with purified MHC molecules and measuring the stability of the MHC-peptide complex. Stability is often assessed through techniques like fluorescence polarization, competitive inhibition assays, or surface plasmon resonance, indicating the binding strength and duration. </p> </li> <li> <span class="sFAQTit">What types of MHC molecules are used in these assays?</span> <p> Both Class I and Class II MHC molecules can be used in binding assays. Class I molecules generally present peptides to CD8+ T cells, while Class II molecules present to CD4+ T cells. The choice of MHC class depends on the specific immune response being studied. </p> </li> <li> <span class="sFAQTit">Can MHC-peptide binding assays predict immune responses?</span> <p> These assays can predict immune responses by identifying peptide epitopes that bind effectively to MHC molecules, suggesting their potential to trigger T-cell activation. However, actual immune response effectiveness can depend on other factors like antigen processing and T-cell receptor variability. </p> </li> <li> <span class="sFAQTit">What role do MHC-peptide binding assays play in vaccine development?</span> <p> In vaccine development, MHC-peptide binding assays are used to identify peptide sequences that bind strongly to MHC molecules, making them good candidates for vaccine antigens. These peptides can elicit a robust immune response, crucial for effective vaccination. </p> </li> <li> <span class="sFAQTit">How are the results of MHC-peptide binding assays interpreted?</span> <p> Results are typically interpreted by comparing the binding affinities of different peptides to MHC molecules. Higher binding affinity indicates a stronger and potentially more effective interaction with T cells, suggesting a greater likelihood of immune activation. </p> </li> </ol> <h2 class="h2_tit page_tab_margin" id="tab5"> Resources </h2> <p> Use the resources in our library to help you understand your options and make critical decisions for your study. </p> <div class="tab_nav"> <span class="tab_choosebg">Videos</span><span>Articles</span> </div> <!---------Videos---------> <div class="tab_cont" style="display:block;"> <div class="row pagerow_pt"> <div class="col-md-4"> <div class="pagerow_pt_unit"> <img loading="lazy" src="../static/img/immunogenicity-overview-of-therapeutic-biologics.jpg" alt="" /> </div> <a href="https://youtu.be/J430752_dTo" target="_blank">Immunogenicity overview of therapeutic biologics</a> </div> </div> </div> <!---------Articles---------> <div class="tab_cont"> <div class="row pagerow_pt"> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-immune-monitoring-for-immunogenicity-assessment-1.jpg" alt="" /> </div> <a href="/immune-monitoring-for-immunogenicity-assessment.html">Immune Monitoring for Immunogenicity Assessment</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-current-immunogenicity-evaluation-systems-a-deep-dive-by-creative-biolabs-1.jpg" alt="" /> </div> <a href="/current-immunogenicity-evaluation-systems.html">Current Immunogenicity Evaluation Systems: A Deep Dive by Creative Biolabs</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-1-in-silico-immunogenicity-assessment-the-leading-edge-approach-to-drug-development-1.jpg" alt="" /> </div> <a href="/in-silico-immunogenicity-assessment-the-leading-edge-approach-to-drug-development.html"><i>In Silico</i> Immunogenicity Assessment: The Leading-edge Approach to Drug Development</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-4-how-to-evaluate-the-immunogenicity-of-therapeutic-protein-drugs-in-vivo-1.jpg" alt="" /> </div> <a href="/how-to-evaluate-the-immunogenicity-of-therapeutic-protein-drugs-in-vivo.html">How to Evaluate the Immunogenicity of Therapeutic Protein Drugs <i>In Vivo</i></a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-5-the-origin-and-detection-methods-of-anti-drug-antibodies-1.jpg" alt="" /> </div> <a href="/the-origin-and-detection-methods-of-anti-drug-antibodies.html">The Origin and Detection Methods of Anti-Drug Antibodies</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-1-8-immunogenic-risk-assessment-of-therapeutic-proteins-1.jpg" alt="" /> </div> <a href="/immunogenic-risk-assessment-of-therapeutic-proteins.html">Immunogenic Risk Assessment of Therapeutic Proteins</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/anti-drug-antibody-introduction-1.jpg" alt="" /> </div> <a href="/anti-drug-antibody-introduction.html">Anti-Drug Antibody Introduction</a> </div> </div> </div> <script> window.addEventListener('load',function(){ // $(function () { $(".tab_nav span").click(function(){ var eqindex=$(this).index(); $(this).addClass("tab_choosebg"); $(this).siblings("span").removeClass("tab_choosebg"); $(".tab_cont").hide().eq(eqindex).show(); }) // }) }); </script><br> <p class="pronote"><i class="fa fa-exclamation-triangle"></i>All listed services and products are For Research Use Only. 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