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A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies
Studying the antibody response to infection or vaccination is essential for developing more effective vaccines and therapeutics. Advances in high-throughput antibody sequencing technologies and immunoinformatic tools now allow the fast and comprehensive analysis of antibody repertoires at high resol...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302312/ https://www.ncbi.nlm.nih.gov/pubmed/37376488 http://dx.doi.org/10.3390/vaccines11061099 |
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author | Ramirez Valdez, Kristel Nzau, Benjamin Dorey-Robinson, Daniel Jarman, Michael Nyagwange, James Schwartz, John C. Freimanis, Graham Steyn, Angela W. Warimwe, George M. Morrison, Liam J. Mwangi, William Charleston, Bryan Bonnet-Di Placido, Marie Hammond, John A. |
author_facet | Ramirez Valdez, Kristel Nzau, Benjamin Dorey-Robinson, Daniel Jarman, Michael Nyagwange, James Schwartz, John C. Freimanis, Graham Steyn, Angela W. Warimwe, George M. Morrison, Liam J. Mwangi, William Charleston, Bryan Bonnet-Di Placido, Marie Hammond, John A. |
author_sort | Ramirez Valdez, Kristel |
collection | PubMed |
description | Studying the antibody response to infection or vaccination is essential for developing more effective vaccines and therapeutics. Advances in high-throughput antibody sequencing technologies and immunoinformatic tools now allow the fast and comprehensive analysis of antibody repertoires at high resolution in any species. Here, we detail a flexible and customizable suite of methods from flow cytometry, single cell sorting, heavy and light chain amplification to antibody sequencing in cattle. These methods were used successfully, including adaptation to the 10x Genomics platform, to isolate native heavy–light chain pairs. When combined with the Ig-Sequence Multi-Species Annotation Tool, this suite represents a powerful toolkit for studying the cattle antibody response with high resolution and precision. Using three workflows, we processed 84, 96, and 8313 cattle B cells from which we sequenced 24, 31, and 4756 antibody heavy–light chain pairs, respectively. Each method has strengths and limitations in terms of the throughput, timeline, specialist equipment, and cost that are each discussed. Moreover, the principles outlined here can be applied to study antibody responses in other mammalian species. |
format | Online Article Text |
id | pubmed-10302312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103023122023-06-29 A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies Ramirez Valdez, Kristel Nzau, Benjamin Dorey-Robinson, Daniel Jarman, Michael Nyagwange, James Schwartz, John C. Freimanis, Graham Steyn, Angela W. Warimwe, George M. Morrison, Liam J. Mwangi, William Charleston, Bryan Bonnet-Di Placido, Marie Hammond, John A. Vaccines (Basel) Article Studying the antibody response to infection or vaccination is essential for developing more effective vaccines and therapeutics. Advances in high-throughput antibody sequencing technologies and immunoinformatic tools now allow the fast and comprehensive analysis of antibody repertoires at high resolution in any species. Here, we detail a flexible and customizable suite of methods from flow cytometry, single cell sorting, heavy and light chain amplification to antibody sequencing in cattle. These methods were used successfully, including adaptation to the 10x Genomics platform, to isolate native heavy–light chain pairs. When combined with the Ig-Sequence Multi-Species Annotation Tool, this suite represents a powerful toolkit for studying the cattle antibody response with high resolution and precision. Using three workflows, we processed 84, 96, and 8313 cattle B cells from which we sequenced 24, 31, and 4756 antibody heavy–light chain pairs, respectively. Each method has strengths and limitations in terms of the throughput, timeline, specialist equipment, and cost that are each discussed. Moreover, the principles outlined here can be applied to study antibody responses in other mammalian species. MDPI 2023-06-14 /pmc/articles/PMC10302312/ /pubmed/37376488 http://dx.doi.org/10.3390/vaccines11061099 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ramirez Valdez, Kristel Nzau, Benjamin Dorey-Robinson, Daniel Jarman, Michael Nyagwange, James Schwartz, John C. Freimanis, Graham Steyn, Angela W. Warimwe, George M. Morrison, Liam J. Mwangi, William Charleston, Bryan Bonnet-Di Placido, Marie Hammond, John A. A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title | A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title_full | A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title_fullStr | A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title_full_unstemmed | A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title_short | A Customizable Suite of Methods to Sequence and Annotate Cattle Antibodies |
title_sort | customizable suite of methods to sequence and annotate cattle antibodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302312/ https://www.ncbi.nlm.nih.gov/pubmed/37376488 http://dx.doi.org/10.3390/vaccines11061099 |
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