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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2020
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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. |
format | Online Article Text |
id | pubmed-7568503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT curtisnicholasc beyondbulksinglechainsequencinggettingatthewholereceptor AT leejiwon beyondbulksinglechainsequencinggettingatthewholereceptor |