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Tandem malonate-based glucosides (TMGs) for membrane protein structural studies
High-resolution membrane protein structures are essential for understanding the molecular basis of diverse biological events and important in drug development. Detergents are usually used to extract these bio-macromolecules from the membranes and maintain them in a soluble and stable state in aqueou...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479785/ https://www.ncbi.nlm.nih.gov/pubmed/28638082 http://dx.doi.org/10.1038/s41598-017-03809-3 |
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author | Hussain, Hazrat Mortensen, Jonas S. Du, Yang Santillan, Claudia Ribeiro, Orquidea Go, Juyeon Hariharan, Parameswaran Loland, Claus J. Guan, Lan Kobilka, Brian K. Byrne, Bernadette Chae, Pil Seok |
author_facet | Hussain, Hazrat Mortensen, Jonas S. Du, Yang Santillan, Claudia Ribeiro, Orquidea Go, Juyeon Hariharan, Parameswaran Loland, Claus J. Guan, Lan Kobilka, Brian K. Byrne, Bernadette Chae, Pil Seok |
author_sort | Hussain, Hazrat |
collection | PubMed |
description | High-resolution membrane protein structures are essential for understanding the molecular basis of diverse biological events and important in drug development. Detergents are usually used to extract these bio-macromolecules from the membranes and maintain them in a soluble and stable state in aqueous solutions for downstream characterization. However, many eukaryotic membrane proteins solubilized in conventional detergents tend to undergo structural degradation, necessitating the development of new amphiphilic agents with enhanced properties. In this study, we designed and synthesized a novel class of glucoside amphiphiles, designated tandem malonate-based glucosides (TMGs). A few TMG agents proved effective at both stabilizing a range of membrane proteins and extracting proteins from the membrane environment. These favourable characteristics, along with synthetic convenience, indicate that these agents have potential in membrane protein research. |
format | Online Article Text |
id | pubmed-5479785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54797852017-06-23 Tandem malonate-based glucosides (TMGs) for membrane protein structural studies Hussain, Hazrat Mortensen, Jonas S. Du, Yang Santillan, Claudia Ribeiro, Orquidea Go, Juyeon Hariharan, Parameswaran Loland, Claus J. Guan, Lan Kobilka, Brian K. Byrne, Bernadette Chae, Pil Seok Sci Rep Article High-resolution membrane protein structures are essential for understanding the molecular basis of diverse biological events and important in drug development. Detergents are usually used to extract these bio-macromolecules from the membranes and maintain them in a soluble and stable state in aqueous solutions for downstream characterization. However, many eukaryotic membrane proteins solubilized in conventional detergents tend to undergo structural degradation, necessitating the development of new amphiphilic agents with enhanced properties. In this study, we designed and synthesized a novel class of glucoside amphiphiles, designated tandem malonate-based glucosides (TMGs). A few TMG agents proved effective at both stabilizing a range of membrane proteins and extracting proteins from the membrane environment. These favourable characteristics, along with synthetic convenience, indicate that these agents have potential in membrane protein research. Nature Publishing Group UK 2017-06-21 /pmc/articles/PMC5479785/ /pubmed/28638082 http://dx.doi.org/10.1038/s41598-017-03809-3 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Hussain, Hazrat Mortensen, Jonas S. Du, Yang Santillan, Claudia Ribeiro, Orquidea Go, Juyeon Hariharan, Parameswaran Loland, Claus J. Guan, Lan Kobilka, Brian K. Byrne, Bernadette Chae, Pil Seok Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title | Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title_full | Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title_fullStr | Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title_full_unstemmed | Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title_short | Tandem malonate-based glucosides (TMGs) for membrane protein structural studies |
title_sort | tandem malonate-based glucosides (tmgs) for membrane protein structural studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479785/ https://www.ncbi.nlm.nih.gov/pubmed/28638082 http://dx.doi.org/10.1038/s41598-017-03809-3 |
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