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pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications
Accurate 3D structures of membrane proteins are essential for comprehending their mechanisms of action and designing specific ligands to modulate their activities. However, these structures are still uncommon due to the involvement of detergents in the sample preparation. Recently, membrane-active p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321531/ https://www.ncbi.nlm.nih.gov/pubmed/37416719 http://dx.doi.org/10.1039/d3sc01890c |
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author | Trinh, Thi Kim Hoang Cabezas, Andres Jorge Joshi, Soumil Catalano, Claudio Siddique, Abu Bakkar Qiu, Weihua Deshmukh, Sanket des Georges, Amedee Guo, Youzhong |
author_facet | Trinh, Thi Kim Hoang Cabezas, Andres Jorge Joshi, Soumil Catalano, Claudio Siddique, Abu Bakkar Qiu, Weihua Deshmukh, Sanket des Georges, Amedee Guo, Youzhong |
author_sort | Trinh, Thi Kim Hoang |
collection | PubMed |
description | Accurate 3D structures of membrane proteins are essential for comprehending their mechanisms of action and designing specific ligands to modulate their activities. However, these structures are still uncommon due to the involvement of detergents in the sample preparation. Recently, membrane-active polymers have emerged as an alternative to detergents, but their incompatibility with low pH and divalent cations has hindered their efficacy. Herein, we describe the design, synthesis, characterization, and application of a new class of pH-tunable membrane-active polymers, NCMNP2a-x. The results demonstrated that NCMNP2a-x could be used for high-resolution single-particle cryo-EM structural analysis of AcrB in various pH conditions and can effectively solubilize BcTSPO with the function preserved. Molecular dynamic simulation is consistent with experimental data that shed great insights into the working mechanism of this class of polymers. These results demonstrated that NCMNP2a-x might have broad applications in membrane protein research. |
format | Online Article Text |
id | pubmed-10321531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-103215312023-07-06 pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications Trinh, Thi Kim Hoang Cabezas, Andres Jorge Joshi, Soumil Catalano, Claudio Siddique, Abu Bakkar Qiu, Weihua Deshmukh, Sanket des Georges, Amedee Guo, Youzhong Chem Sci Chemistry Accurate 3D structures of membrane proteins are essential for comprehending their mechanisms of action and designing specific ligands to modulate their activities. However, these structures are still uncommon due to the involvement of detergents in the sample preparation. Recently, membrane-active polymers have emerged as an alternative to detergents, but their incompatibility with low pH and divalent cations has hindered their efficacy. Herein, we describe the design, synthesis, characterization, and application of a new class of pH-tunable membrane-active polymers, NCMNP2a-x. The results demonstrated that NCMNP2a-x could be used for high-resolution single-particle cryo-EM structural analysis of AcrB in various pH conditions and can effectively solubilize BcTSPO with the function preserved. Molecular dynamic simulation is consistent with experimental data that shed great insights into the working mechanism of this class of polymers. These results demonstrated that NCMNP2a-x might have broad applications in membrane protein research. The Royal Society of Chemistry 2023-06-09 /pmc/articles/PMC10321531/ /pubmed/37416719 http://dx.doi.org/10.1039/d3sc01890c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Trinh, Thi Kim Hoang Cabezas, Andres Jorge Joshi, Soumil Catalano, Claudio Siddique, Abu Bakkar Qiu, Weihua Deshmukh, Sanket des Georges, Amedee Guo, Youzhong pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title | pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title_full | pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title_fullStr | pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title_full_unstemmed | pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title_short | pH-tunable membrane-active polymers, NCMNP2a-x, and their potential membrane protein applications |
title_sort | ph-tunable membrane-active polymers, ncmnp2a-x, and their potential membrane protein applications |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321531/ https://www.ncbi.nlm.nih.gov/pubmed/37416719 http://dx.doi.org/10.1039/d3sc01890c |
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