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Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein
Nanodisc technology has dramatically advanced the analysis of molecular interactions for membrane proteins. A nanodisc is designed as a vehicle for membrane proteins that provide a native-like phospholipid environment and better thermostability in a detergent-free buffer. This enables the determinat...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356912/ https://www.ncbi.nlm.nih.gov/pubmed/37468499 http://dx.doi.org/10.1038/s41598-023-38547-2 |
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author | Nakagawa, Fuhito Kikkawa, Marin Chen, Sisi Miyashita, Yasuomi Hamaguchi-Suzuki, Norie Shibuya, Minami Yamashita, Soichi Nagase, Lisa Yasuda, Satoshi Shiroishi, Mitsunori Senda, Toshiya Ito, Keisuke Murata, Takeshi Ogasawara, Satoshi |
author_facet | Nakagawa, Fuhito Kikkawa, Marin Chen, Sisi Miyashita, Yasuomi Hamaguchi-Suzuki, Norie Shibuya, Minami Yamashita, Soichi Nagase, Lisa Yasuda, Satoshi Shiroishi, Mitsunori Senda, Toshiya Ito, Keisuke Murata, Takeshi Ogasawara, Satoshi |
author_sort | Nakagawa, Fuhito |
collection | PubMed |
description | Nanodisc technology has dramatically advanced the analysis of molecular interactions for membrane proteins. A nanodisc is designed as a vehicle for membrane proteins that provide a native-like phospholipid environment and better thermostability in a detergent-free buffer. This enables the determination of the thermodynamic and kinetic parameters of small molecule binding by surface plasmon resonance. In this study, we generated a nanodisc specific anti-MSP (membrane scaffold protein) monoclonal antibody biND5 for molecular interaction analysis of nanodiscs. The antibody, biND5 bound to various types of nanodiscs with sub-nanomolar to nanomolar affinity. Epitope mapping analysis revealed specific recognition of 8 amino acid residues in the exposed helix-4 structure of MSP. Further, we performed kinetics binding analysis between adenosine A(2a) receptor reconstituted nanodiscs and small molecule antagonist ZM241385 using biND5 immobilized sensor chips. These results show that biND5 facilitates the molecular interaction kinetics analysis of membrane proteins substituted in nanodiscs. |
format | Online Article Text |
id | pubmed-10356912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103569122023-07-21 Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein Nakagawa, Fuhito Kikkawa, Marin Chen, Sisi Miyashita, Yasuomi Hamaguchi-Suzuki, Norie Shibuya, Minami Yamashita, Soichi Nagase, Lisa Yasuda, Satoshi Shiroishi, Mitsunori Senda, Toshiya Ito, Keisuke Murata, Takeshi Ogasawara, Satoshi Sci Rep Article Nanodisc technology has dramatically advanced the analysis of molecular interactions for membrane proteins. A nanodisc is designed as a vehicle for membrane proteins that provide a native-like phospholipid environment and better thermostability in a detergent-free buffer. This enables the determination of the thermodynamic and kinetic parameters of small molecule binding by surface plasmon resonance. In this study, we generated a nanodisc specific anti-MSP (membrane scaffold protein) monoclonal antibody biND5 for molecular interaction analysis of nanodiscs. The antibody, biND5 bound to various types of nanodiscs with sub-nanomolar to nanomolar affinity. Epitope mapping analysis revealed specific recognition of 8 amino acid residues in the exposed helix-4 structure of MSP. Further, we performed kinetics binding analysis between adenosine A(2a) receptor reconstituted nanodiscs and small molecule antagonist ZM241385 using biND5 immobilized sensor chips. These results show that biND5 facilitates the molecular interaction kinetics analysis of membrane proteins substituted in nanodiscs. Nature Publishing Group UK 2023-07-19 /pmc/articles/PMC10356912/ /pubmed/37468499 http://dx.doi.org/10.1038/s41598-023-38547-2 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 Nakagawa, Fuhito Kikkawa, Marin Chen, Sisi Miyashita, Yasuomi Hamaguchi-Suzuki, Norie Shibuya, Minami Yamashita, Soichi Nagase, Lisa Yasuda, Satoshi Shiroishi, Mitsunori Senda, Toshiya Ito, Keisuke Murata, Takeshi Ogasawara, Satoshi Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title | Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title_full | Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title_fullStr | Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title_full_unstemmed | Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title_short | Anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
title_sort | anti-nanodisc antibodies specifically capture nanodiscs and facilitate molecular interaction kinetics studies for membrane protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356912/ https://www.ncbi.nlm.nih.gov/pubmed/37468499 http://dx.doi.org/10.1038/s41598-023-38547-2 |
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