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NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating 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: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327083/
https://www.ncbi.nlm.nih.gov/pubmed/37425915
http://dx.doi.org/10.1101/2023.06.28.546392
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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 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-103270832023-07-08 NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating 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. bioRxiv 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 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. Cold Spring Harbor Laboratory 2023-06-30 /pmc/articles/PMC10327083/ /pubmed/37425915 http://dx.doi.org/10.1101/2023.06.28.546392 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
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.
NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title_full NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title_fullStr NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title_full_unstemmed NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title_short NeuroMabSeq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scFvs for neuroscience research
title_sort neuromabseq: high volume acquisition, processing, and curation of hybridoma sequences and their use in generating recombinant monoclonal antibodies and scfvs for neuroscience research
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327083/
https://www.ncbi.nlm.nih.gov/pubmed/37425915
http://dx.doi.org/10.1101/2023.06.28.546392
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