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Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors

Detergents enable the purification of membrane proteins and are indispensable reagents in structural biology. Even though a large variety of detergents have been developed in the last century, the challenge remains to identify guidelines that allow fine-tuning of detergents for individual applicatio...

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Autores principales: Urner, Leonhard H., Liko, Idlir, Yen, Hsin-Yung, Hoi, Kin-Kuan, Bolla, Jani Reddy, Gault, Joseph, Almeida, Fernando Gonçalves, Schweder, Marc-Philip, Shutin, Denis, Ehrmann, Svenja, Haag, Rainer, Robinson, Carol V., Pagel, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987200/
https://www.ncbi.nlm.nih.gov/pubmed/31992701
http://dx.doi.org/10.1038/s41467-020-14424-8
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author Urner, Leonhard H.
Liko, Idlir
Yen, Hsin-Yung
Hoi, Kin-Kuan
Bolla, Jani Reddy
Gault, Joseph
Almeida, Fernando Gonçalves
Schweder, Marc-Philip
Shutin, Denis
Ehrmann, Svenja
Haag, Rainer
Robinson, Carol V.
Pagel, Kevin
author_facet Urner, Leonhard H.
Liko, Idlir
Yen, Hsin-Yung
Hoi, Kin-Kuan
Bolla, Jani Reddy
Gault, Joseph
Almeida, Fernando Gonçalves
Schweder, Marc-Philip
Shutin, Denis
Ehrmann, Svenja
Haag, Rainer
Robinson, Carol V.
Pagel, Kevin
author_sort Urner, Leonhard H.
collection PubMed
description Detergents enable the purification of membrane proteins and are indispensable reagents in structural biology. Even though a large variety of detergents have been developed in the last century, the challenge remains to identify guidelines that allow fine-tuning of detergents for individual applications in membrane protein research. Addressing this challenge, here we introduce the family of oligoglycerol detergents (OGDs). Native mass spectrometry (MS) reveals that the modular OGD architecture offers the ability to control protein purification and to preserve interactions with native membrane lipids during purification. In addition to a broad range of bacterial membrane proteins, OGDs also enable the purification and analysis of a functional G-protein coupled receptor (GPCR). Moreover, given the modular design of these detergents, we anticipate fine-tuning of their properties for specific applications in structural biology. Seen from a broader perspective, this represents a significant advance for the investigation of membrane proteins and their interactions with lipids.
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spelling pubmed-69872002020-01-30 Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors Urner, Leonhard H. Liko, Idlir Yen, Hsin-Yung Hoi, Kin-Kuan Bolla, Jani Reddy Gault, Joseph Almeida, Fernando Gonçalves Schweder, Marc-Philip Shutin, Denis Ehrmann, Svenja Haag, Rainer Robinson, Carol V. Pagel, Kevin Nat Commun Article Detergents enable the purification of membrane proteins and are indispensable reagents in structural biology. Even though a large variety of detergents have been developed in the last century, the challenge remains to identify guidelines that allow fine-tuning of detergents for individual applications in membrane protein research. Addressing this challenge, here we introduce the family of oligoglycerol detergents (OGDs). Native mass spectrometry (MS) reveals that the modular OGD architecture offers the ability to control protein purification and to preserve interactions with native membrane lipids during purification. In addition to a broad range of bacterial membrane proteins, OGDs also enable the purification and analysis of a functional G-protein coupled receptor (GPCR). Moreover, given the modular design of these detergents, we anticipate fine-tuning of their properties for specific applications in structural biology. Seen from a broader perspective, this represents a significant advance for the investigation of membrane proteins and their interactions with lipids. Nature Publishing Group UK 2020-01-28 /pmc/articles/PMC6987200/ /pubmed/31992701 http://dx.doi.org/10.1038/s41467-020-14424-8 Text en © The Author(s) 2020 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
Urner, Leonhard H.
Liko, Idlir
Yen, Hsin-Yung
Hoi, Kin-Kuan
Bolla, Jani Reddy
Gault, Joseph
Almeida, Fernando Gonçalves
Schweder, Marc-Philip
Shutin, Denis
Ehrmann, Svenja
Haag, Rainer
Robinson, Carol V.
Pagel, Kevin
Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title_full Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title_fullStr Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title_full_unstemmed Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title_short Modular detergents tailor the purification and structural analysis of membrane proteins including G-protein coupled receptors
title_sort modular detergents tailor the purification and structural analysis of membrane proteins including g-protein coupled receptors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987200/
https://www.ncbi.nlm.nih.gov/pubmed/31992701
http://dx.doi.org/10.1038/s41467-020-14424-8
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