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Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change
Protein-peptide interactions are involved in many fundamental cellular functions and constitute promising drug targets. Here, we provide a detailed protocol for the cost-effective preparation of a cellulose-based solid support for synthesis of nanoscale to micromolar-scale peptide libraries. Their s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219886/ https://www.ncbi.nlm.nih.gov/pubmed/34189471 http://dx.doi.org/10.1016/j.xpro.2021.100605 |
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author | Schulte, Clemens Khayenko, Vladimir Gupta, Amit Jean Maric, Hans Michael |
author_facet | Schulte, Clemens Khayenko, Vladimir Gupta, Amit Jean Maric, Hans Michael |
author_sort | Schulte, Clemens |
collection | PubMed |
description | Protein-peptide interactions are involved in many fundamental cellular functions and constitute promising drug targets. Here, we provide a detailed protocol for the cost-effective preparation of a cellulose-based solid support for synthesis of nanoscale to micromolar-scale peptide libraries. Their subsequent use for high-throughput protein interaction screening as well as affinity determination in solution provides binding data for thousands of unique peptides with a turnover of 1 to 2 weeks, thereby facilitating in vitro assessment and development of high-affinity binders. For complete details on the use and execution of this protocol, please refer to Schulte et al., (2020) |
format | Online Article Text |
id | pubmed-8219886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82198862021-06-28 Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change Schulte, Clemens Khayenko, Vladimir Gupta, Amit Jean Maric, Hans Michael STAR Protoc Protocol Protein-peptide interactions are involved in many fundamental cellular functions and constitute promising drug targets. Here, we provide a detailed protocol for the cost-effective preparation of a cellulose-based solid support for synthesis of nanoscale to micromolar-scale peptide libraries. Their subsequent use for high-throughput protein interaction screening as well as affinity determination in solution provides binding data for thousands of unique peptides with a turnover of 1 to 2 weeks, thereby facilitating in vitro assessment and development of high-affinity binders. For complete details on the use and execution of this protocol, please refer to Schulte et al., (2020) Elsevier 2021-06-15 /pmc/articles/PMC8219886/ /pubmed/34189471 http://dx.doi.org/10.1016/j.xpro.2021.100605 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Schulte, Clemens Khayenko, Vladimir Gupta, Amit Jean Maric, Hans Michael Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title | Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title_full | Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title_fullStr | Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title_full_unstemmed | Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title_short | Low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
title_sort | low-cost synthesis of peptide libraries and their use for binding studies via temperature-related intensity change |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219886/ https://www.ncbi.nlm.nih.gov/pubmed/34189471 http://dx.doi.org/10.1016/j.xpro.2021.100605 |
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