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Beyond bulk single-chain sequencing: Getting at the whole receptor

Recent advancements in paired B-cell receptor sequencing technologies have accelerated the development of simpler, high-throughput pipelines for generating native antibody heavy and light chain pairs used to elucidate novel antibodies and provide insights into antibody response against pathogenic ta...

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Detalles Bibliográficos
Autores principales: Curtis, Nicholas C., Lee, Jiwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568503/
https://www.ncbi.nlm.nih.gov/pubmed/33102951
http://dx.doi.org/10.1016/j.coisb.2020.10.008
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author Curtis, Nicholas C.
Lee, Jiwon
author_facet Curtis, Nicholas C.
Lee, Jiwon
author_sort Curtis, Nicholas C.
collection PubMed
description Recent advancements in paired B-cell receptor sequencing technologies have accelerated the development of simpler, high-throughput pipelines for generating native antibody heavy and light chain pairs used to elucidate novel antibodies and provide insights into antibody response against pathogenic targets. These technologies involve single-cell isolation, using either single wells or emulsified droplets to maintain physical separation of individual cells, followed by sequencing. The development of novel single wells and emulsion-based workflows addresses key challenges by improving throughput of single-cell analyses, reducing method complexity, and integrating functional assays into existing workflows. Enabled by paired B-cell receptor sequencing, functional characterization of pathogen-specific antibodies reveals immunological insights beyond bulk sequencing.
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spelling pubmed-75685032020-10-19 Beyond bulk single-chain sequencing: Getting at the whole receptor Curtis, Nicholas C. Lee, Jiwon Curr Opin Syst Biol Article Recent advancements in paired B-cell receptor sequencing technologies have accelerated the development of simpler, high-throughput pipelines for generating native antibody heavy and light chain pairs used to elucidate novel antibodies and provide insights into antibody response against pathogenic targets. These technologies involve single-cell isolation, using either single wells or emulsified droplets to maintain physical separation of individual cells, followed by sequencing. The development of novel single wells and emulsion-based workflows addresses key challenges by improving throughput of single-cell analyses, reducing method complexity, and integrating functional assays into existing workflows. Enabled by paired B-cell receptor sequencing, functional characterization of pathogen-specific antibodies reveals immunological insights beyond bulk sequencing. Elsevier Ltd. 2020-12 2020-10-17 /pmc/articles/PMC7568503/ /pubmed/33102951 http://dx.doi.org/10.1016/j.coisb.2020.10.008 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Curtis, Nicholas C.
Lee, Jiwon
Beyond bulk single-chain sequencing: Getting at the whole receptor
title Beyond bulk single-chain sequencing: Getting at the whole receptor
title_full Beyond bulk single-chain sequencing: Getting at the whole receptor
title_fullStr Beyond bulk single-chain sequencing: Getting at the whole receptor
title_full_unstemmed Beyond bulk single-chain sequencing: Getting at the whole receptor
title_short Beyond bulk single-chain sequencing: Getting at the whole receptor
title_sort beyond bulk single-chain sequencing: getting at the whole receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568503/
https://www.ncbi.nlm.nih.gov/pubmed/33102951
http://dx.doi.org/10.1016/j.coisb.2020.10.008
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