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High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research

The Neuroscience Monoclonal Antibody Sequencing Initiative (NeuroMabSeq) is a concerted effort to determine and make publicly available hybridoma-derived sequences of monoclonal antibodies (mAbs) valuable to neuroscience research. Over 30 years of research and development efforts including those at...

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Autores principales: Mitchell, Keith G., Gong, Belvin, Hunter, Samuel S., Burkart-Waco, Diana, Gavira-O’Neill, Clara E., Templeton, Kayla M., Goethel, Madeline E., Bzymek, Malgorzata, MacNiven, Leah M., Murray, Karl D., Settles, Matthew L., Froenicke, Lutz, Trimmer, James S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533561/
https://www.ncbi.nlm.nih.gov/pubmed/37758930
http://dx.doi.org/10.1038/s41598-023-43233-4
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author Mitchell, Keith G.
Gong, Belvin
Hunter, Samuel S.
Burkart-Waco, Diana
Gavira-O’Neill, Clara E.
Templeton, Kayla M.
Goethel, Madeline E.
Bzymek, Malgorzata
MacNiven, Leah M.
Murray, Karl D.
Settles, Matthew L.
Froenicke, Lutz
Trimmer, James S.
author_facet Mitchell, Keith G.
Gong, Belvin
Hunter, Samuel S.
Burkart-Waco, Diana
Gavira-O’Neill, Clara E.
Templeton, Kayla M.
Goethel, Madeline E.
Bzymek, Malgorzata
MacNiven, Leah M.
Murray, Karl D.
Settles, Matthew L.
Froenicke, Lutz
Trimmer, James S.
author_sort Mitchell, Keith G.
collection PubMed
description The Neuroscience Monoclonal Antibody Sequencing Initiative (NeuroMabSeq) is a concerted effort to determine and make publicly available hybridoma-derived sequences of monoclonal antibodies (mAbs) valuable to neuroscience research. Over 30 years of research and development efforts including those at the UC Davis/NIH NeuroMab Facility have resulted in the generation of a large collection of mouse mAbs validated for neuroscience research. To enhance dissemination and increase the utility of this valuable resource, we applied a high-throughput DNA sequencing approach to determine immunoglobulin heavy and light chain variable domain sequences from source hybridoma cells. The resultant set of sequences was made publicly available as a searchable DNA sequence database (neuromabseq.ucdavis.edu) for sharing, analysis and use in downstream applications. We enhanced the utility, transparency, and reproducibility of the existing mAb collection by using these sequences to develop recombinant mAbs. This enabled their subsequent engineering into alternate forms with distinct utility, including alternate modes of detection in multiplexed labeling, and as miniaturized single chain variable fragments or scFvs. The NeuroMabSeq website and database and the corresponding recombinant antibody collection together serve as a public DNA sequence repository of mouse mAb heavy and light chain variable domain sequences and as an open resource for enhancing dissemination and utility of this valuable collection of validated mAbs.
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spelling pubmed-105335612023-09-29 High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research Mitchell, Keith G. Gong, Belvin Hunter, Samuel S. Burkart-Waco, Diana Gavira-O’Neill, Clara E. Templeton, Kayla M. Goethel, Madeline E. Bzymek, Malgorzata MacNiven, Leah M. Murray, Karl D. Settles, Matthew L. Froenicke, Lutz Trimmer, James S. Sci Rep Article The Neuroscience Monoclonal Antibody Sequencing Initiative (NeuroMabSeq) is a concerted effort to determine and make publicly available hybridoma-derived sequences of monoclonal antibodies (mAbs) valuable to neuroscience research. Over 30 years of research and development efforts including those at the UC Davis/NIH NeuroMab Facility have resulted in the generation of a large collection of mouse mAbs validated for neuroscience research. To enhance dissemination and increase the utility of this valuable resource, we applied a high-throughput DNA sequencing approach to determine immunoglobulin heavy and light chain variable domain sequences from source hybridoma cells. The resultant set of sequences was made publicly available as a searchable DNA sequence database (neuromabseq.ucdavis.edu) for sharing, analysis and use in downstream applications. We enhanced the utility, transparency, and reproducibility of the existing mAb collection by using these sequences to develop recombinant mAbs. This enabled their subsequent engineering into alternate forms with distinct utility, including alternate modes of detection in multiplexed labeling, and as miniaturized single chain variable fragments or scFvs. The NeuroMabSeq website and database and the corresponding recombinant antibody collection together serve as a public DNA sequence repository of mouse mAb heavy and light chain variable domain sequences and as an open resource for enhancing dissemination and utility of this valuable collection of validated mAbs. Nature Publishing Group UK 2023-09-27 /pmc/articles/PMC10533561/ /pubmed/37758930 http://dx.doi.org/10.1038/s41598-023-43233-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mitchell, Keith G.
Gong, Belvin
Hunter, Samuel S.
Burkart-Waco, Diana
Gavira-O’Neill, Clara E.
Templeton, Kayla M.
Goethel, Madeline E.
Bzymek, Malgorzata
MacNiven, Leah M.
Murray, Karl D.
Settles, Matthew L.
Froenicke, Lutz
Trimmer, James S.
High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title_full High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title_fullStr High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title_full_unstemmed High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title_short High-volume hybridoma sequencing on the NeuroMabSeq platform enables efficient generation of recombinant monoclonal antibodies and scFvs for neuroscience research
title_sort high-volume hybridoma sequencing on the neuromabseq platform enables efficient generation of recombinant monoclonal antibodies and scfvs for neuroscience research
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533561/
https://www.ncbi.nlm.nih.gov/pubmed/37758930
http://dx.doi.org/10.1038/s41598-023-43233-4
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