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Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M
Mouse monoclonal antibody M4M was recently designed to block human TRPM4 channel. The polypeptide for generating M4M is composed of peptide A1 between the transmembrane segment 5 (S5) and the pore, and a second peptide A2 between the pore and the transmembrane segment 6 (S6). Using peptide microarra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666640/ https://www.ncbi.nlm.nih.gov/pubmed/36380063 http://dx.doi.org/10.1038/s41598-022-22077-4 |
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author | Wei, Shunhui Behn, Julian Poore, Charlene Priscilla Low, See Wee Nilius, Bernd Fan, Hao Liao, Ping |
author_facet | Wei, Shunhui Behn, Julian Poore, Charlene Priscilla Low, See Wee Nilius, Bernd Fan, Hao Liao, Ping |
author_sort | Wei, Shunhui |
collection | PubMed |
description | Mouse monoclonal antibody M4M was recently designed to block human TRPM4 channel. The polypeptide for generating M4M is composed of peptide A1 between the transmembrane segment 5 (S5) and the pore, and a second peptide A2 between the pore and the transmembrane segment 6 (S6). Using peptide microarray, a 4-amino acid sequence EPGF within the A2 was identified to be the binding epitope for M4M. Substitution of EPGF with other amino acids greatly reduced binding affinity. Structural analysis of human TRPM4 structure indicates that EPGF is located externally to the channel pore. A1 is close to the EPGF binding epitope in space, albeit separated by a 37-amino acid peptide. Electrophysiological study reveals that M4M could block human TRPM4, but with no effect on rodent TRPM4 which shares a different amino acid sequence ERGS for the binding motif. Our results demonstrate that M4M is a specific inhibitor for human TRPM4. |
format | Online Article Text |
id | pubmed-9666640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96666402022-11-17 Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M Wei, Shunhui Behn, Julian Poore, Charlene Priscilla Low, See Wee Nilius, Bernd Fan, Hao Liao, Ping Sci Rep Article Mouse monoclonal antibody M4M was recently designed to block human TRPM4 channel. The polypeptide for generating M4M is composed of peptide A1 between the transmembrane segment 5 (S5) and the pore, and a second peptide A2 between the pore and the transmembrane segment 6 (S6). Using peptide microarray, a 4-amino acid sequence EPGF within the A2 was identified to be the binding epitope for M4M. Substitution of EPGF with other amino acids greatly reduced binding affinity. Structural analysis of human TRPM4 structure indicates that EPGF is located externally to the channel pore. A1 is close to the EPGF binding epitope in space, albeit separated by a 37-amino acid peptide. Electrophysiological study reveals that M4M could block human TRPM4, but with no effect on rodent TRPM4 which shares a different amino acid sequence ERGS for the binding motif. Our results demonstrate that M4M is a specific inhibitor for human TRPM4. Nature Publishing Group UK 2022-11-15 /pmc/articles/PMC9666640/ /pubmed/36380063 http://dx.doi.org/10.1038/s41598-022-22077-4 Text en © The Author(s) 2022 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 Wei, Shunhui Behn, Julian Poore, Charlene Priscilla Low, See Wee Nilius, Bernd Fan, Hao Liao, Ping Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title | Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title_full | Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title_fullStr | Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title_full_unstemmed | Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title_short | Binding epitope for recognition of human TRPM4 channel by monoclonal antibody M4M |
title_sort | binding epitope for recognition of human trpm4 channel by monoclonal antibody m4m |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666640/ https://www.ncbi.nlm.nih.gov/pubmed/36380063 http://dx.doi.org/10.1038/s41598-022-22077-4 |
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