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Polyamine detergents tailored for native mass spectrometry studies of membrane proteins
Native mass spectrometry (MS) is a powerful technique for interrogating membrane protein complexes and their interactions with other molecules. A key aspect of the technique is the ability to preserve native-like structures and noncovalent interactions, which can be challenging depending on the choi...
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/PMC10502129/ https://www.ncbi.nlm.nih.gov/pubmed/37709761 http://dx.doi.org/10.1038/s41467-023-41429-w |
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author | Zhu, Yun Peng, Bo-Ji Kumar, Smriti Stover, Lauren Chang, Jing-Yuan Lyu, Jixing Zhang, Tianqi Schrecke, Samantha Azizov, Djavdat Russell, David H. Fang, Lei Laganowsky, Arthur |
author_facet | Zhu, Yun Peng, Bo-Ji Kumar, Smriti Stover, Lauren Chang, Jing-Yuan Lyu, Jixing Zhang, Tianqi Schrecke, Samantha Azizov, Djavdat Russell, David H. Fang, Lei Laganowsky, Arthur |
author_sort | Zhu, Yun |
collection | PubMed |
description | Native mass spectrometry (MS) is a powerful technique for interrogating membrane protein complexes and their interactions with other molecules. A key aspect of the technique is the ability to preserve native-like structures and noncovalent interactions, which can be challenging depending on the choice of detergent. Different strategies have been employed to reduce charge on protein complexes to minimize activation and preserve non-covalent interactions. Here, we report the synthesis of a class of polyamine detergents tailored for native MS studies of membrane proteins. These detergents, a series of spermine covalently attached to various alkyl tails, are exceptional charge-reducing molecules, exhibiting a ten-fold enhanced potency over spermine. Addition of polyamine detergents to proteins solubilized in maltoside detergents results in improved, charge-reduced native mass spectra and reduced dissociation of subunits. Polyamine detergents open new opportunities to investigate membrane proteins in different detergent environments that have thwarted previous native MS studies. |
format | Online Article Text |
id | pubmed-10502129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105021292023-09-16 Polyamine detergents tailored for native mass spectrometry studies of membrane proteins Zhu, Yun Peng, Bo-Ji Kumar, Smriti Stover, Lauren Chang, Jing-Yuan Lyu, Jixing Zhang, Tianqi Schrecke, Samantha Azizov, Djavdat Russell, David H. Fang, Lei Laganowsky, Arthur Nat Commun Article Native mass spectrometry (MS) is a powerful technique for interrogating membrane protein complexes and their interactions with other molecules. A key aspect of the technique is the ability to preserve native-like structures and noncovalent interactions, which can be challenging depending on the choice of detergent. Different strategies have been employed to reduce charge on protein complexes to minimize activation and preserve non-covalent interactions. Here, we report the synthesis of a class of polyamine detergents tailored for native MS studies of membrane proteins. These detergents, a series of spermine covalently attached to various alkyl tails, are exceptional charge-reducing molecules, exhibiting a ten-fold enhanced potency over spermine. Addition of polyamine detergents to proteins solubilized in maltoside detergents results in improved, charge-reduced native mass spectra and reduced dissociation of subunits. Polyamine detergents open new opportunities to investigate membrane proteins in different detergent environments that have thwarted previous native MS studies. Nature Publishing Group UK 2023-09-14 /pmc/articles/PMC10502129/ /pubmed/37709761 http://dx.doi.org/10.1038/s41467-023-41429-w 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhu, Yun Peng, Bo-Ji Kumar, Smriti Stover, Lauren Chang, Jing-Yuan Lyu, Jixing Zhang, Tianqi Schrecke, Samantha Azizov, Djavdat Russell, David H. Fang, Lei Laganowsky, Arthur Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title | Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title_full | Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title_fullStr | Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title_full_unstemmed | Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title_short | Polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
title_sort | polyamine detergents tailored for native mass spectrometry studies of membrane proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502129/ https://www.ncbi.nlm.nih.gov/pubmed/37709761 http://dx.doi.org/10.1038/s41467-023-41429-w |
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