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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...

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Detalles Bibliográficos
Autores principales: Shen, Luhui, Zhao, Zhan-Gong, Lainson, John C., Brown, Justin R., Sykes, Kathryn F., Johnston, Stephen Albert, Diehnelt, Chris W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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