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Production of high-complexity frameshift neoantigen peptide microarrays
Parallel measurement of large numbers of antigen–antibody interactions are increasingly enabled by peptide microarray technologies. Our group has developed an in situ synthesized peptide microarray of >400 000 frameshift neoantigens using mask-based photolithographic peptide synthesis, to profile...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056171/ https://www.ncbi.nlm.nih.gov/pubmed/35518269 http://dx.doi.org/10.1039/d0ra05267a |
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author | Shen, Luhui Zhao, Zhan-Gong Lainson, John C. Brown, Justin R. Sykes, Kathryn F. Johnston, Stephen Albert Diehnelt, Chris W. |
author_facet | Shen, Luhui Zhao, Zhan-Gong Lainson, John C. Brown, Justin R. Sykes, Kathryn F. Johnston, Stephen Albert Diehnelt, Chris W. |
author_sort | Shen, Luhui |
collection | PubMed |
description | Parallel measurement of large numbers of antigen–antibody interactions are increasingly enabled by peptide microarray technologies. Our group has developed an in situ synthesized peptide microarray of >400 000 frameshift neoantigens using mask-based photolithographic peptide synthesis, to profile patient specific neoantigen reactive antibodies in a single assay. The system produces 208 replicate mircoarrays per wafer and is capable of producing multiple wafers per synthetic lot to routinely synthesize over 300 million peptides simultaneously. In this report, we demonstrate the feasibility of the system for detecting peripheral-blood antibody binding to frameshift neoantigens across multiple synthetic lots. |
format | Online Article Text |
id | pubmed-9056171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90561712022-05-04 Production of high-complexity frameshift neoantigen peptide microarrays Shen, Luhui Zhao, Zhan-Gong Lainson, John C. Brown, Justin R. Sykes, Kathryn F. Johnston, Stephen Albert Diehnelt, Chris W. RSC Adv Chemistry Parallel measurement of large numbers of antigen–antibody interactions are increasingly enabled by peptide microarray technologies. Our group has developed an in situ synthesized peptide microarray of >400 000 frameshift neoantigens using mask-based photolithographic peptide synthesis, to profile patient specific neoantigen reactive antibodies in a single assay. The system produces 208 replicate mircoarrays per wafer and is capable of producing multiple wafers per synthetic lot to routinely synthesize over 300 million peptides simultaneously. In this report, we demonstrate the feasibility of the system for detecting peripheral-blood antibody binding to frameshift neoantigens across multiple synthetic lots. The Royal Society of Chemistry 2020-08-11 /pmc/articles/PMC9056171/ /pubmed/35518269 http://dx.doi.org/10.1039/d0ra05267a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Shen, Luhui Zhao, Zhan-Gong Lainson, John C. Brown, Justin R. Sykes, Kathryn F. Johnston, Stephen Albert Diehnelt, Chris W. Production of high-complexity frameshift neoantigen peptide microarrays |
title | Production of high-complexity frameshift neoantigen peptide microarrays |
title_full | Production of high-complexity frameshift neoantigen peptide microarrays |
title_fullStr | Production of high-complexity frameshift neoantigen peptide microarrays |
title_full_unstemmed | Production of high-complexity frameshift neoantigen peptide microarrays |
title_short | Production of high-complexity frameshift neoantigen peptide microarrays |
title_sort | production of high-complexity frameshift neoantigen peptide microarrays |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056171/ https://www.ncbi.nlm.nih.gov/pubmed/35518269 http://dx.doi.org/10.1039/d0ra05267a |
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