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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...

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Detalles Bibliográficos
Autores principales: Schulte, Clemens, Khayenko, Vladimir, Gupta, Amit Jean, Maric, Hans Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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)
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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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