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High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry
Toward the goal of increasing the throughput of high-resolution mass characterization of intact antibodies, we developed a RapidFire–mass spectrometry (MS) assay using electrospray ionization. We achieved unprecedented screening throughput as fast as 15 s/sample, which is an order of magnitude impro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211930/ https://www.ncbi.nlm.nih.gov/pubmed/32327606 http://dx.doi.org/10.1073/pnas.1917383117 |
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author | Sawyer, William S. Srikumar, Neha Carver, Joseph Chu, Phillip Y. Shen, Amy Xu, Ankai Williams, Ambrose J. Spiess, Christoph Wu, Cong Liu, Yichin Tran, John C. |
author_facet | Sawyer, William S. Srikumar, Neha Carver, Joseph Chu, Phillip Y. Shen, Amy Xu, Ankai Williams, Ambrose J. Spiess, Christoph Wu, Cong Liu, Yichin Tran, John C. |
author_sort | Sawyer, William S. |
collection | PubMed |
description | Toward the goal of increasing the throughput of high-resolution mass characterization of intact antibodies, we developed a RapidFire–mass spectrometry (MS) assay using electrospray ionization. We achieved unprecedented screening throughput as fast as 15 s/sample, which is an order of magnitude improvement over conventional liquid chromatography (LC)-MS approaches. The screening enabled intact mass determination as accurate as 7 ppm with baseline resolution at the glycoform level for intact antibodies. We utilized this assay to characterize and perform relative quantitation of antibody species from 248 samples of 62 different cell line clones at four time points in 2 h using RapidFire–time-of-flight MS screening. The screening enabled selection of clones with the highest purity of bispecific antibody production and the results significantly correlated with conventional LC-MS results. In addition, analyzing antibodies from a complex plasma sample using affinity-RapidFire-MS was also demonstrated and qualified. In summary, the platform affords high-throughput analyses of antibodies, including bispecific antibodies and potential mispaired side products, in cell culture media, or other complex matrices. |
format | Online Article Text |
id | pubmed-7211930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-72119302020-05-15 High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry Sawyer, William S. Srikumar, Neha Carver, Joseph Chu, Phillip Y. Shen, Amy Xu, Ankai Williams, Ambrose J. Spiess, Christoph Wu, Cong Liu, Yichin Tran, John C. Proc Natl Acad Sci U S A Biological Sciences Toward the goal of increasing the throughput of high-resolution mass characterization of intact antibodies, we developed a RapidFire–mass spectrometry (MS) assay using electrospray ionization. We achieved unprecedented screening throughput as fast as 15 s/sample, which is an order of magnitude improvement over conventional liquid chromatography (LC)-MS approaches. The screening enabled intact mass determination as accurate as 7 ppm with baseline resolution at the glycoform level for intact antibodies. We utilized this assay to characterize and perform relative quantitation of antibody species from 248 samples of 62 different cell line clones at four time points in 2 h using RapidFire–time-of-flight MS screening. The screening enabled selection of clones with the highest purity of bispecific antibody production and the results significantly correlated with conventional LC-MS results. In addition, analyzing antibodies from a complex plasma sample using affinity-RapidFire-MS was also demonstrated and qualified. In summary, the platform affords high-throughput analyses of antibodies, including bispecific antibodies and potential mispaired side products, in cell culture media, or other complex matrices. National Academy of Sciences 2020-05-05 2020-04-23 /pmc/articles/PMC7211930/ /pubmed/32327606 http://dx.doi.org/10.1073/pnas.1917383117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Sawyer, William S. Srikumar, Neha Carver, Joseph Chu, Phillip Y. Shen, Amy Xu, Ankai Williams, Ambrose J. Spiess, Christoph Wu, Cong Liu, Yichin Tran, John C. High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title | High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title_full | High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title_fullStr | High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title_full_unstemmed | High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title_short | High-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
title_sort | high-throughput antibody screening from complex matrices using intact protein electrospray mass spectrometry |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211930/ https://www.ncbi.nlm.nih.gov/pubmed/32327606 http://dx.doi.org/10.1073/pnas.1917383117 |
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