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Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing

High-throughput antibody repertoire analysis via next-generation sequencing is a key method in understanding humoral immunity. Errors introduced during library preparation and sequencing can be corrected with molecular amplification fingerprinting using unique molecular identifiers. Here, we provide...

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Autores principales: Werner, Anja, Schäfer, Simon, Gleußner, Nina, Nimmerjahn, Falk, Winkler, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010798/
https://www.ncbi.nlm.nih.gov/pubmed/35434659
http://dx.doi.org/10.1016/j.xpro.2022.101277
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author Werner, Anja
Schäfer, Simon
Gleußner, Nina
Nimmerjahn, Falk
Winkler, Thomas H.
author_facet Werner, Anja
Schäfer, Simon
Gleußner, Nina
Nimmerjahn, Falk
Winkler, Thomas H.
author_sort Werner, Anja
collection PubMed
description High-throughput antibody repertoire analysis via next-generation sequencing is a key method in understanding humoral immunity. Errors introduced during library preparation and sequencing can be corrected with molecular amplification fingerprinting using unique molecular identifiers. Here, we provide a step-by-step protocol for laboratory and bioinformatic workflows to perform sequencing in murine cells with isotype-specific primers, obtaining total and isotype-specific B cell receptor repertoires. This enables the examination of isotype-dependent immune responses and improves the understanding of underlying mechanisms in humoral immunity. For complete details on the use and execution of this protocol, please refer to Khan et al. (2016).
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spelling pubmed-90107982022-04-16 Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing Werner, Anja Schäfer, Simon Gleußner, Nina Nimmerjahn, Falk Winkler, Thomas H. STAR Protoc Protocol High-throughput antibody repertoire analysis via next-generation sequencing is a key method in understanding humoral immunity. Errors introduced during library preparation and sequencing can be corrected with molecular amplification fingerprinting using unique molecular identifiers. Here, we provide a step-by-step protocol for laboratory and bioinformatic workflows to perform sequencing in murine cells with isotype-specific primers, obtaining total and isotype-specific B cell receptor repertoires. This enables the examination of isotype-dependent immune responses and improves the understanding of underlying mechanisms in humoral immunity. For complete details on the use and execution of this protocol, please refer to Khan et al. (2016). Elsevier 2022-04-09 /pmc/articles/PMC9010798/ /pubmed/35434659 http://dx.doi.org/10.1016/j.xpro.2022.101277 Text en © 2022 The Author(s) 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 Protocol
Werner, Anja
Schäfer, Simon
Gleußner, Nina
Nimmerjahn, Falk
Winkler, Thomas H.
Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title_full Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title_fullStr Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title_full_unstemmed Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title_short Determining immunoglobulin-specific B cell receptor repertoire of murine splenocytes by next-generation sequencing
title_sort determining immunoglobulin-specific b cell receptor repertoire of murine splenocytes by next-generation sequencing
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010798/
https://www.ncbi.nlm.nih.gov/pubmed/35434659
http://dx.doi.org/10.1016/j.xpro.2022.101277
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