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Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding
Yeast display can serve as a powerful tool to assess the binding of peptides to the major histocompatibility complex (pMHC) and pMHC-T-cell receptor binding. However, this approach is often limited by the need to optimize MHC proteins for yeast surface expression, which can be laborious and may not...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971316/ https://www.ncbi.nlm.nih.gov/pubmed/36649909 http://dx.doi.org/10.1016/j.jbc.2023.102913 |
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author | Huisman, Brooke D. Balivada, Pallavi A. Birnbaum, Michael E. |
author_facet | Huisman, Brooke D. Balivada, Pallavi A. Birnbaum, Michael E. |
author_sort | Huisman, Brooke D. |
collection | PubMed |
description | Yeast display can serve as a powerful tool to assess the binding of peptides to the major histocompatibility complex (pMHC) and pMHC-T-cell receptor binding. However, this approach is often limited by the need to optimize MHC proteins for yeast surface expression, which can be laborious and may not yield productive results. Here we present a second-generation yeast display platform for class II MHC molecules (MHC-II), which decouples MHC-II expression from yeast-expressed peptides, referred to as “peptide display.” Peptide display obviates the need for yeast-specific MHC optimizations and increases the scale of MHC-II alleles available for use in yeast display screens. Because MHC identity is separated from the peptide library, a further benefit of this platform is the ability to assess a single library of peptides against any MHC-II. We demonstrate the utility of the peptide display platform across MHC-II proteins, screening HLA-DR, HLA-DP, and HLA-DQ alleles. We further explore parameters of selections, including reagent dependencies, MHC avidity, and use of competitor peptides. In summary, this approach presents an advance in the throughput and accessibility of screening peptide-MHC-II binding. |
format | Online Article Text |
id | pubmed-9971316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99713162023-03-01 Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding Huisman, Brooke D. Balivada, Pallavi A. Birnbaum, Michael E. J Biol Chem Methods and Resources Yeast display can serve as a powerful tool to assess the binding of peptides to the major histocompatibility complex (pMHC) and pMHC-T-cell receptor binding. However, this approach is often limited by the need to optimize MHC proteins for yeast surface expression, which can be laborious and may not yield productive results. Here we present a second-generation yeast display platform for class II MHC molecules (MHC-II), which decouples MHC-II expression from yeast-expressed peptides, referred to as “peptide display.” Peptide display obviates the need for yeast-specific MHC optimizations and increases the scale of MHC-II alleles available for use in yeast display screens. Because MHC identity is separated from the peptide library, a further benefit of this platform is the ability to assess a single library of peptides against any MHC-II. We demonstrate the utility of the peptide display platform across MHC-II proteins, screening HLA-DR, HLA-DP, and HLA-DQ alleles. We further explore parameters of selections, including reagent dependencies, MHC avidity, and use of competitor peptides. In summary, this approach presents an advance in the throughput and accessibility of screening peptide-MHC-II binding. American Society for Biochemistry and Molecular Biology 2023-01-14 /pmc/articles/PMC9971316/ /pubmed/36649909 http://dx.doi.org/10.1016/j.jbc.2023.102913 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Methods and Resources Huisman, Brooke D. Balivada, Pallavi A. Birnbaum, Michael E. Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title | Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title_full | Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title_fullStr | Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title_full_unstemmed | Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title_short | Yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-MHC-II binding |
title_sort | yeast display platform with expression of linear peptide epitopes for high-throughput assessment of peptide-mhc-ii binding |
topic | Methods and Resources |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971316/ https://www.ncbi.nlm.nih.gov/pubmed/36649909 http://dx.doi.org/10.1016/j.jbc.2023.102913 |
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