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A peptide library is constructed by synthesizing the oligopeptide sequences from overlapping and non-overlapping segments of a target protein. And the ability to bind the corresponding antibody of interest is tested. This method is especially suited to profiling epitopes of a defined protein for candidate antibodies in a high-throughput way. It is quick, cost-effective and will be an excellent option for the case of small amounts of your precious samples. </p> <h2 class="h2_tit page_tab_margin" id="tab1"> Background </h2> <p> A peptide/protein microarray, also commonly known as peptide/protein chip, goes by displaying the target peptides on a solid surface (often a glass or plastic chip). This platform delivers a full compatibility of the chips based on overlapping peptide libraries (or non-overlapping peptide libraries) of your target protein or your target proteins by utilizing a flexible peptide synthesis technology. There is a variety of peptide libraries for a target protein and the construction of a peptide library could be obtained by different approaches. The overlapping peptide library is the most commonly used and other libraries are also available at Creative Biolabs, including truncation library, alanine scan library, random library, positional scan library and scrambled library. Basically, the microarrays epitope mapping analysis involves the following major steps, which are the synthesis of a peptide library, then binding analysis, followed by bioinformatics-based data analysis, and constructing initial results. In addition, our unique technology ensures greater reproducibility of this assay, and reduces background signal and improves assay performance in sensitivity, dynamic range, and variance. </p> <p class="ServiceShowPic"> <img src="static/img/CreMap-Epitope-Mapping-by-Peptide-microarray-service-1.png" width="500" height="211" loading="lazy" alt="Principle of microarray technology." /> Fig.1 Principle of microarray technology. </p> <h2 class="h2_tit page_tab_margin" id="tab2"> CreMap™ Peptide/Protein Microarray Service </h2> <p> Compared with ELISA or other ligand binding assays, our CreMap™ peptide/protein microarray platform features a competitive price and high-throughput assays. It can detect thousands of interactions in a single run and enables higher sensitivity with lower cost and allows customized plate chips by providing different forms and shapes (e.g. direct assays, sandwich assays, bridging assays). Furthermore, your established assay protocols can be easily transferred to our service platform by supplying microliter amounts sample of your protein/antibodies/sera. </p> <h2 class="h2_tit page_tab_margin" id="tab3"> Applications of CreMap™ Peptide/Protein Microarray Service </h2> <ul class="ullist"> <li> Mapping epitopes present on monoclonal antibodies, bacteria, viruses, parasites, tumor markers and enzymes. </li> <li> Screening the best monoclonal antibody (mAb) from a panel by characterizing the binding strength or target specificity. </li> <li> Designing vaccines. </li> </ul> <h2 class="h2_tit page_tab_margin" id="tab4"> Ordering Process of Our CreMap™ Peptide/Protein Microarray Service </h2> <ul class="ullist"> <li> Creative Biolabs’ doctoral consultants will communicate with clients in time to understand the project properly. </li> <li> Creative Biolabs’ doctoral consultants will provide you with a reasonable and economical solution. </li> <li> The professional team of Creative Biolabs will accept and store the samples or synthetic information you provide. </li> <li> The professional team of Creative Biolabs will perform all of the experimental steps according to the previously provided program. </li> <li> A complete analysis report and experimental data will be delivered after this assay. </li> </ul> <br /> <p class="ServiceShowPic"> <img src="static/img/CreMap-Epitope-Mapping-by-Peptide-microarray-service-2.png" width="560" height="73" loading="lazy" alt="CreMap™ Epitope Mapping by Peptide Microarray" /> </p> <p> Based on our CreMap™ technical platform, Creative Biolabs is dedicated to providing high-class epitope mapping service by using peptide microarray. If you are now trying to figure out epitopes on an antigen, or if you are interested in our platform, please <a class="inquiry-button">contact us</a>. A formal feedback will be sent back as soon as possible </p> <p> Other optional <a href="/CreMap-B-Cell-Epitope-Mapping-Service.html">CreMap™ B cell epitope mapping services</a>: </p> <ul class="ullist"> <li> <a href="/cremap-epitope-mapping-by-limited-proteolysis-coupled-with-mass-spectrometry.html">CreMap™ Epitope Mapping by Limited Proteolysis coupled with Mass Spectrometry</a> </li> <li> <a href="/cremap-epitope-mapping-service-by-hydrogen-deuterium-exchange.html">CreMap™ Epitope Mapping by Hydrogen/Deuterium Exchange</a> </li> <li> <a href="/cremap-epitope-mapping-by-nuclear-magnetic-resonance-analysis.html">CreMap™ Epitope Mapping by Nuclear Magnetic Resonance (NMR) Analysis</a> </li> <li> <a href="/cremap-epitope-mapping-by-surface-plasmon-resonance.html">CreMap™ Epitope Mapping by Surface Plasmon Resonance</a> </li> <li> <a href="/cremap-epitope-mapping-service-by-x-ray-crystallography.html">CreMap™ Epitope Mapping by X-ray Crystallography</a> </li> <li> <a href="/CreMap-Alanine-Scanning-Mutagenesis-Mapping-Service.html">CreMap™ Epitope Mapping by Alanine Scanning Mutagenesis</a> </li> <li> <a href="/epitope-mapping-on-a-microfluidic-peptide-microarray.html">CreMap™ Epitope Mapping by Microfluidic Peptide Microarray</a> </li> <li> <a href="/cremap-epitope-mapping-by-surface-display-technique.html">CreMap™ Epitope Mapping by Surface Display Technique</a> </li> <li> <a href="/linear-b-cell-epitopes.html">Linear B-Cell Epitopes</a> </li> <li> <a href="/conformational-b-cell-epitopes.html">Conformational B-Cell Epitopes</a> </li> </ul> <h2 class="h2_tit page_tab_margin" id="tab5"> Published Data </h2> <ul class="ullist"> <li> <strong>ASFV Epitope Mapping by Peptides Microarrays</strong> </li> </ul> <p class="show-center"> <img loading="lazy" src="static/img/1-2-8-3-1-1-epitope-mapping-by-peptide-microarray-2.jpg" width="550" height="164" alt="" />Fig. 2 Fluorescent image of peptide array chips after reaction with A) ASF positive pig serum sample (S31), and B) ASF negative pig serum sample. (Cloé Desmet, 2024) </p> <p> The article addresses the critical need for an effective vaccine against African swine fever virus (ASFV) by applying high-density peptide microarrays for epitope mapping. This method enabled the identification of protective antigens that are recognized by antibodies from infected animals, which is pivotal for vaccine development. Results indicated specific ASFV proteins like p54 that are already targets for vaccine development, and new epitopes were identified that could potentially improve vaccine designs. This epitope mapping by peptide microarrays provided a detailed and high-throughput analysis of antibody interactions at the amino acid level, which is crucial for tailoring vaccines that elicit strong protective immune responses in pigs against various ASFV strains. </p> <div class="reference"> <strong>Reference</strong> <ol class="ollist decimal"> <li> Desmet, Cloé, et al. "ASFV epitope mapping by high density peptides microarrays." <em>Virus Research</em> 339 (2024): 199287. </li> </ol> </div> <script type="text/javascript"> window.addEventListener('load',function(){ faqlist(4); }); </script> <h2 class="h2_tit page_tab_margin" id="tab6"> FAQ </h2> <ol class="ollist faqlist"> <li> <span class="sFAQTit">What is epitope mapping by peptide/protein microarrays?</span> <p> Epitope mapping by peptide/protein microarrays involves the use of microarray technology to identify the specific parts of antigens recognized by antibodies. This technique allows for the simultaneous screening of thousands of peptides or proteins, helping to pinpoint which sequences within a protein are involved in immune recognition. </p> </li> <li> <span class="sFAQTit">How do peptide/protein microarrays work for epitope mapping?</span> <p> In peptide/protein microarrays, synthetic peptides or proteins are printed in a dense array on a solid surface. These arrays are then exposed to sera or antibodies, and interactions are detected using labeled secondary antibodies that fluoresce under specific conditions. The fluorescence intensity at each spot indicates the strength of antibody binding, identifying potential epitopes. </p> </li> <li> <span class="sFAQTit">What are the advantages of using microarrays for epitope mapping?</span> <p> Microarrays allow for high-throughput screening, meaning many peptides can be tested simultaneously, which accelerates the discovery process. This method is also highly sensitive and can detect even weak interactions between antibodies and antigens. It requires only small amounts of antibodies and antigens, making it resource-efficient. </p> </li> <li> <span class="sFAQTit">Can peptide/protein microarrays differentiate between conformational and linear epitopes?</span> <p> While peptide microarrays are excellent for identifying linear epitopes, they are less effective for conformational epitopes, which depend on the three-dimensional folding of proteins. Protein microarrays that preserve the native structure of proteins are more suitable for identifying conformational epitopes. </p> </li> <li> <span class="sFAQTit">What types of research can benefit from epitope mapping using microarrays?</span> <p> Epitope mapping by microarrays is invaluable in vaccine development, diagnostic research, allergy research, and autoimmunity studies. It helps in identifying which parts of a pathogen or allergen elicit an immune response, guiding the development of targeted therapies and vaccines. </p> </li> <li> <span class="sFAQTit">How are peptide/protein microarrays designed?</span> <p> Peptide/protein microarrays are designed based on the sequence of the target protein. Peptides—usually 15 to 20 amino acids long—are synthesized to cover the entire length of the protein, often with overlapping sequences to ensure complete coverage. These peptides are then chemically bonded to a solid surface, like glass or plastic. </p> </li> <li> <span class="sFAQTit">Are there specific sample preparations required for microarray epitope mapping?</span> <p> Sample preparation for microarray epitope mapping typically involves purifying antibodies or sera to remove components that might cause non-specific binding. Samples may also need to be diluted to optimal concentrations to balance sensitivity and specificity. </p> </li> </ol> <h2 class="h2_tit page_tab_margin" id="tab7"> 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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