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Cycloalkane-modified amphiphilic polymers provide direct extraction of membrane proteins for CryoEM analysis
被引:0
|作者:
Anna J. Higgins
Alex J. Flynn
Anaïs Marconnet
Laura J. Musgrove
Vincent L. G. Postis
Jonathan D. Lippiat
Chun-wa Chung
Tom Ceska
Manuela Zoonens
Frank Sobott
Stephen P. Muench
机构:
[1] School of Biomedical Sciences,
[2] Faculty of Biological Sciences & Astbury Centre for Structural and Molecular Biology,undefined
[3] University of Leeds,undefined
[4] Université de Paris,undefined
[5] Laboratoire de Biologie Physico-Chimique des Protéines Membranaires,undefined
[6] CNRS,undefined
[7] UMR 7099,undefined
[8] Institut de Biologie Physico-Chimique,undefined
[9] Fondation Edmond de Rothschild pour le dévelopement de la recherche scientifique,undefined
[10] Wellcome Centre for Anti-Infectives Research,undefined
[11] Drug Discovery Unit,undefined
[12] Division of Biological Chemistry and Drug Discovery,undefined
[13] University of Dundee,undefined
[14] GlaxoSmithKline,undefined
[15] Gunnels Wood Road,undefined
[16] UCB Pharma,undefined
[17] School of Molecular and Cellular Biology,undefined
[18] Faculty of Biological Sciences & Astbury Centre for Structural and Molecular Biology,undefined
[19] University of Leeds,undefined
来源:
Communications Biology
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摘要:
Membrane proteins are essential for cellular growth, signalling and homeostasis, making up a large proportion of therapeutic targets. However, the necessity for a solubilising agent to extract them from the membrane creates challenges in their structural and functional study. Although amphipols have been very effective for single-particle electron cryo-microscopy (cryoEM) and mass spectrometry, they rely on initial detergent extraction before exchange into the amphipol environment. Therefore, circumventing this pre-requirement would be a big advantage. Here we use an alternative type of amphipol: a cycloalkane-modified amphiphile polymer (CyclAPol) to extract Escherichia coli AcrB directly from the membrane and demonstrate that the protein can be isolated in a one-step purification with the resultant cryoEM structure achieving 3.2 Å resolution. Together this work shows that cycloalkane amphipols provide a powerful approach for the study of membrane proteins, allowing native extraction and high-resolution structure determination by cryoEM.
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