中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A Chemical Strategy for Amphiphile Replacement in Membrane Protein Research

文献类型:期刊论文

作者Xue, Dongxian2,3,4,6; Wang, Jingjing2,4,5,6; Song, Xiyong4,7; Wang, Wei1; Hu, Tao2,3,4,6; Ye, Lintao2; Liu, Yang2; Zhou, Qingtong2; Zhou, Fang2,3,4,6; Jiang, Zhong-Xing1
刊名LANGMUIR
出版日期2019-03-26
卷号35期号:12页码:4319-4327
ISSN号0743-7463
DOI10.1021/acs.langmuir.8b04072
通讯作者Liu, Zhi-Jie(liuzhj@shanghaitech.edu.cn) ; Tao, Houchao(taohch@shanghaitech.edu.cn)
英文摘要Membrane mimics are indispensable tools in the structural and functional understanding of membrane proteins (MPs). Given stringent requirements of integral MP manipulations, amphiphile replacement is often required in sample preparation for various biophysical purposes. Current protocols generally rely on physical methodologies and rarely reach complete replacement. In comparison, we report herein a chemical alternative that facilitates the exhaustive exchange of membrane-mimicking systems for MP reconstitution. This method, named sacrifice-replacement strategy, was enabled by a class of chemically cleavable detergents (CCDs), derived from the disulfide incorporation in the traditional detergent n-dodecyl-beta-D-maltopyranoside. The representative CCD behaved well in both solubilizing the diverse alpha-helical human G protein coupled receptors and refolding of the beta-barrel bacterial outer membrane protein X, and more importantly, it could also be readily degraded under mild conditions. By this means, the A(2A) adenosine receptor was successfully reconstituted into a series of commercial detergents for stabilization screening and nanodiscs for electron microscopy analysis. Featured by the simplicity and compatibility, this CCD-mediated strategy would later find more applications when being integrated in other biophysics studies.
WOS关键词PHOSPHOLIPID-BILAYER NANODISCS ; DETERGENTS ; QUANTIFICATION ; MECHANISMS ; DIGESTION ; COMPLEX ; OMPX
资助项目Shanghai Municipal Government ; ShanghaiTech University ; NSFC[21672147] ; National Key R&D Program of China[2018YFA0507000]
WOS研究方向Chemistry ; Materials Science
语种英语
WOS记录号WOS:000462944900014
出版者AMER CHEMICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/290007]  
专题中国科学院上海药物研究所
通讯作者Liu, Zhi-Jie; Tao, Houchao
作者单位1.Wuhan Univ, Sch Pharmaceut Sci, Hubei Prov Engn & Technol Res Ctr Fluorinated Pha, Wuhan 430071, Hubei, Peoples R China
2.ShanghaiTech Univ, iHuman Inst, Ren Bldg,393 Middle Huaxia Rd, Shanghai 201210, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Mat Med, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China
4.Univ Chinese Acad Sci, 19A,Yuquan Rd, Beijing 100049, Peoples R China
5.Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Shanghai 200031, Peoples R China
6.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
7.Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing 100101, Peoples R China
推荐引用方式
GB/T 7714
Xue, Dongxian,Wang, Jingjing,Song, Xiyong,et al. A Chemical Strategy for Amphiphile Replacement in Membrane Protein Research[J]. LANGMUIR,2019,35(12):4319-4327.
APA Xue, Dongxian.,Wang, Jingjing.,Song, Xiyong.,Wang, Wei.,Hu, Tao.,...&Tao, Houchao.(2019).A Chemical Strategy for Amphiphile Replacement in Membrane Protein Research.LANGMUIR,35(12),4319-4327.
MLA Xue, Dongxian,et al."A Chemical Strategy for Amphiphile Replacement in Membrane Protein Research".LANGMUIR 35.12(2019):4319-4327.

入库方式: OAI收割

来源:上海药物研究所

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