Loading…

Folding and stabilizing membrane proteins in amphipol A8-35

•Amphipathic polymers (amphipols) are relevant tools for membrane protein studies.•Folding membrane proteins overexpressed in inclusion bodies using amphipols.•Replacing detergents by amphipols increases the stability of membrane proteins. Membrane proteins (MPs) are important pharmacological target...

Full description

Saved in:
Bibliographic Details
Published in:Methods (San Diego, Calif.) Calif.), 2018-09, Vol.147, p.95-105
Main Authors: Le Bon, Christel, Marconnet, Anaïs, Masscheleyn, Sandrine, Popot, Jean-Luc, Zoonens, Manuela
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533
cites cdi_FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533
container_end_page 105
container_issue
container_start_page 95
container_title Methods (San Diego, Calif.)
container_volume 147
creator Le Bon, Christel
Marconnet, Anaïs
Masscheleyn, Sandrine
Popot, Jean-Luc
Zoonens, Manuela
description •Amphipathic polymers (amphipols) are relevant tools for membrane protein studies.•Folding membrane proteins overexpressed in inclusion bodies using amphipols.•Replacing detergents by amphipols increases the stability of membrane proteins. Membrane proteins (MPs) are important pharmacological targets because of their involvement in many essential cellular processes whose dysfunction can lead to a large variety of diseases. A detailed knowledge of the structure of MPs and the molecular mechanisms of their activity is essential to the design of new therapeutic agents. However, studying MPs in vitro is challenging, because it generally implies their overexpression under a functional form, followed by their extraction from membranes and purification. Targeting an overexpressed MP to a membrane is often toxic and expression yields tend to be limited. One alternative is the formation of inclusion bodies (IBs) in the cytosol of the cell, from which MPs need then to be folded to their native conformation before structural and functional analysis can be contemplated. Folding MPs targeted to IBs is a difficult task. Specially designed amphipathic polymers called ‘amphipols’ (APols), which have been initially developed with the view of improving the stability of MPs in aqueous solutions compared to detergents, can be used to fold both α-helical and β-barrel MPs. APols represent an interesting novel amphipathic medium, in which high folding yields can be achieved. In this review, the properties of APol A8-35 and of the complexes they form with MPs are summarized. An overview of the most important studies reported so far using A8-35 to fold MPs is presented. Finally, from a practical point of view, a detailed description of the folding and trapping methods is given.
doi_str_mv 10.1016/j.ymeth.2018.04.012
format article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_02363736v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1046202317304668</els_id><sourcerecordid>2028957357</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533</originalsourceid><addsrcrecordid>eNp9kFtLwzAUgIMobk5_gSB91IfWXJpLER_GcE4Y-KLPIU1PXUYvs-kG89ebuumjEEhO-M7tQ-ia4IRgIu7Xyb6GfpVQTFSC0wQTeoLGBGc8zgjDp8M7FTHFlI3QhfdrjAMi1Tka0UxIxZUco4d5WxWu-YhMU0S-N7mr3NcQ11DnnWkg2nRtD67xkWsiU29WbtNW0VTFjF-is9JUHq6O9wS9z5_eZot4-fr8MpsuY8sy1seytKB4WghqDNCUshREzrgSuLAiNWFUyamx1jCwkvJSKQtCcq5KS5TgjE3Q3aHuylR607nadHvdGqcX06Ue_sKGgkkmdiSwtwc2jP25Bd_r2nkLVRVWabdeBxsq45KFM0HsgNqu9b6D8q82wXowrNf6x7AeDGuc6qAvZN0cG2zzGoq_nF-lAXg8ABCU7Bx02lsHjYXCdWB7XbTu3wbfi1-LEQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2028957357</pqid></control><display><type>article</type><title>Folding and stabilizing membrane proteins in amphipol A8-35</title><source>ScienceDirect Freedom Collection</source><creator>Le Bon, Christel ; Marconnet, Anaïs ; Masscheleyn, Sandrine ; Popot, Jean-Luc ; Zoonens, Manuela</creator><creatorcontrib>Le Bon, Christel ; Marconnet, Anaïs ; Masscheleyn, Sandrine ; Popot, Jean-Luc ; Zoonens, Manuela</creatorcontrib><description>•Amphipathic polymers (amphipols) are relevant tools for membrane protein studies.•Folding membrane proteins overexpressed in inclusion bodies using amphipols.•Replacing detergents by amphipols increases the stability of membrane proteins. Membrane proteins (MPs) are important pharmacological targets because of their involvement in many essential cellular processes whose dysfunction can lead to a large variety of diseases. A detailed knowledge of the structure of MPs and the molecular mechanisms of their activity is essential to the design of new therapeutic agents. However, studying MPs in vitro is challenging, because it generally implies their overexpression under a functional form, followed by their extraction from membranes and purification. Targeting an overexpressed MP to a membrane is often toxic and expression yields tend to be limited. One alternative is the formation of inclusion bodies (IBs) in the cytosol of the cell, from which MPs need then to be folded to their native conformation before structural and functional analysis can be contemplated. Folding MPs targeted to IBs is a difficult task. Specially designed amphipathic polymers called ‘amphipols’ (APols), which have been initially developed with the view of improving the stability of MPs in aqueous solutions compared to detergents, can be used to fold both α-helical and β-barrel MPs. APols represent an interesting novel amphipathic medium, in which high folding yields can be achieved. In this review, the properties of APol A8-35 and of the complexes they form with MPs are summarized. An overview of the most important studies reported so far using A8-35 to fold MPs is presented. Finally, from a practical point of view, a detailed description of the folding and trapping methods is given.</description><identifier>ISSN: 1046-2023</identifier><identifier>EISSN: 1095-9130</identifier><identifier>DOI: 10.1016/j.ymeth.2018.04.012</identifier><identifier>PMID: 29678587</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biochemistry, Molecular Biology ; Inclusion bodies ; Life Sciences ; Membrane Proteins - chemistry ; Native conformation ; Overexpression ; Polymers - chemistry ; Propylamines - chemistry ; Protein Conformation, alpha-Helical ; Protein Denaturation ; Protein Folding ; Protein Stability ; Refolding ; Stability ; Surfactants</subject><ispartof>Methods (San Diego, Calif.), 2018-09, Vol.147, p.95-105</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533</citedby><cites>FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533</cites><orcidid>0000-0002-2922-7554 ; 0000-0003-2648-7868</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29678587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02363736$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Le Bon, Christel</creatorcontrib><creatorcontrib>Marconnet, Anaïs</creatorcontrib><creatorcontrib>Masscheleyn, Sandrine</creatorcontrib><creatorcontrib>Popot, Jean-Luc</creatorcontrib><creatorcontrib>Zoonens, Manuela</creatorcontrib><title>Folding and stabilizing membrane proteins in amphipol A8-35</title><title>Methods (San Diego, Calif.)</title><addtitle>Methods</addtitle><description>•Amphipathic polymers (amphipols) are relevant tools for membrane protein studies.•Folding membrane proteins overexpressed in inclusion bodies using amphipols.•Replacing detergents by amphipols increases the stability of membrane proteins. Membrane proteins (MPs) are important pharmacological targets because of their involvement in many essential cellular processes whose dysfunction can lead to a large variety of diseases. A detailed knowledge of the structure of MPs and the molecular mechanisms of their activity is essential to the design of new therapeutic agents. However, studying MPs in vitro is challenging, because it generally implies their overexpression under a functional form, followed by their extraction from membranes and purification. Targeting an overexpressed MP to a membrane is often toxic and expression yields tend to be limited. One alternative is the formation of inclusion bodies (IBs) in the cytosol of the cell, from which MPs need then to be folded to their native conformation before structural and functional analysis can be contemplated. Folding MPs targeted to IBs is a difficult task. Specially designed amphipathic polymers called ‘amphipols’ (APols), which have been initially developed with the view of improving the stability of MPs in aqueous solutions compared to detergents, can be used to fold both α-helical and β-barrel MPs. APols represent an interesting novel amphipathic medium, in which high folding yields can be achieved. In this review, the properties of APol A8-35 and of the complexes they form with MPs are summarized. An overview of the most important studies reported so far using A8-35 to fold MPs is presented. Finally, from a practical point of view, a detailed description of the folding and trapping methods is given.</description><subject>Biochemistry, Molecular Biology</subject><subject>Inclusion bodies</subject><subject>Life Sciences</subject><subject>Membrane Proteins - chemistry</subject><subject>Native conformation</subject><subject>Overexpression</subject><subject>Polymers - chemistry</subject><subject>Propylamines - chemistry</subject><subject>Protein Conformation, alpha-Helical</subject><subject>Protein Denaturation</subject><subject>Protein Folding</subject><subject>Protein Stability</subject><subject>Refolding</subject><subject>Stability</subject><subject>Surfactants</subject><issn>1046-2023</issn><issn>1095-9130</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kFtLwzAUgIMobk5_gSB91IfWXJpLER_GcE4Y-KLPIU1PXUYvs-kG89ebuumjEEhO-M7tQ-ia4IRgIu7Xyb6GfpVQTFSC0wQTeoLGBGc8zgjDp8M7FTHFlI3QhfdrjAMi1Tka0UxIxZUco4d5WxWu-YhMU0S-N7mr3NcQ11DnnWkg2nRtD67xkWsiU29WbtNW0VTFjF-is9JUHq6O9wS9z5_eZot4-fr8MpsuY8sy1seytKB4WghqDNCUshREzrgSuLAiNWFUyamx1jCwkvJSKQtCcq5KS5TgjE3Q3aHuylR607nadHvdGqcX06Ue_sKGgkkmdiSwtwc2jP25Bd_r2nkLVRVWabdeBxsq45KFM0HsgNqu9b6D8q82wXowrNf6x7AeDGuc6qAvZN0cG2zzGoq_nF-lAXg8ABCU7Bx02lsHjYXCdWB7XbTu3wbfi1-LEQ</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Le Bon, Christel</creator><creator>Marconnet, Anaïs</creator><creator>Masscheleyn, Sandrine</creator><creator>Popot, Jean-Luc</creator><creator>Zoonens, Manuela</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-2922-7554</orcidid><orcidid>https://orcid.org/0000-0003-2648-7868</orcidid></search><sort><creationdate>20180901</creationdate><title>Folding and stabilizing membrane proteins in amphipol A8-35</title><author>Le Bon, Christel ; Marconnet, Anaïs ; Masscheleyn, Sandrine ; Popot, Jean-Luc ; Zoonens, Manuela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biochemistry, Molecular Biology</topic><topic>Inclusion bodies</topic><topic>Life Sciences</topic><topic>Membrane Proteins - chemistry</topic><topic>Native conformation</topic><topic>Overexpression</topic><topic>Polymers - chemistry</topic><topic>Propylamines - chemistry</topic><topic>Protein Conformation, alpha-Helical</topic><topic>Protein Denaturation</topic><topic>Protein Folding</topic><topic>Protein Stability</topic><topic>Refolding</topic><topic>Stability</topic><topic>Surfactants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le Bon, Christel</creatorcontrib><creatorcontrib>Marconnet, Anaïs</creatorcontrib><creatorcontrib>Masscheleyn, Sandrine</creatorcontrib><creatorcontrib>Popot, Jean-Luc</creatorcontrib><creatorcontrib>Zoonens, Manuela</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Methods (San Diego, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le Bon, Christel</au><au>Marconnet, Anaïs</au><au>Masscheleyn, Sandrine</au><au>Popot, Jean-Luc</au><au>Zoonens, Manuela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Folding and stabilizing membrane proteins in amphipol A8-35</atitle><jtitle>Methods (San Diego, Calif.)</jtitle><addtitle>Methods</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>147</volume><spage>95</spage><epage>105</epage><pages>95-105</pages><issn>1046-2023</issn><eissn>1095-9130</eissn><abstract>•Amphipathic polymers (amphipols) are relevant tools for membrane protein studies.•Folding membrane proteins overexpressed in inclusion bodies using amphipols.•Replacing detergents by amphipols increases the stability of membrane proteins. Membrane proteins (MPs) are important pharmacological targets because of their involvement in many essential cellular processes whose dysfunction can lead to a large variety of diseases. A detailed knowledge of the structure of MPs and the molecular mechanisms of their activity is essential to the design of new therapeutic agents. However, studying MPs in vitro is challenging, because it generally implies their overexpression under a functional form, followed by their extraction from membranes and purification. Targeting an overexpressed MP to a membrane is often toxic and expression yields tend to be limited. One alternative is the formation of inclusion bodies (IBs) in the cytosol of the cell, from which MPs need then to be folded to their native conformation before structural and functional analysis can be contemplated. Folding MPs targeted to IBs is a difficult task. Specially designed amphipathic polymers called ‘amphipols’ (APols), which have been initially developed with the view of improving the stability of MPs in aqueous solutions compared to detergents, can be used to fold both α-helical and β-barrel MPs. APols represent an interesting novel amphipathic medium, in which high folding yields can be achieved. In this review, the properties of APol A8-35 and of the complexes they form with MPs are summarized. An overview of the most important studies reported so far using A8-35 to fold MPs is presented. Finally, from a practical point of view, a detailed description of the folding and trapping methods is given.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29678587</pmid><doi>10.1016/j.ymeth.2018.04.012</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2922-7554</orcidid><orcidid>https://orcid.org/0000-0003-2648-7868</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1046-2023
ispartof Methods (San Diego, Calif.), 2018-09, Vol.147, p.95-105
issn 1046-2023
1095-9130
language eng
recordid cdi_hal_primary_oai_HAL_hal_02363736v1
source ScienceDirect Freedom Collection
subjects Biochemistry, Molecular Biology
Inclusion bodies
Life Sciences
Membrane Proteins - chemistry
Native conformation
Overexpression
Polymers - chemistry
Propylamines - chemistry
Protein Conformation, alpha-Helical
Protein Denaturation
Protein Folding
Protein Stability
Refolding
Stability
Surfactants
title Folding and stabilizing membrane proteins in amphipol A8-35
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T10%3A59%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Folding%20and%20stabilizing%20membrane%20proteins%20in%20amphipol%20A8-35&rft.jtitle=Methods%20(San%20Diego,%20Calif.)&rft.au=Le%20Bon,%20Christel&rft.date=2018-09-01&rft.volume=147&rft.spage=95&rft.epage=105&rft.pages=95-105&rft.issn=1046-2023&rft.eissn=1095-9130&rft_id=info:doi/10.1016/j.ymeth.2018.04.012&rft_dat=%3Cproquest_hal_p%3E2028957357%3C/proquest_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c393t-7fce854d62aae24234e6b35860dc64a130752acca3ec725f88ce67558fc186533%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2028957357&rft_id=info:pmid/29678587&rfr_iscdi=true