Single-particle cryo-EM studies of transmembrane proteins in SMA copolymer nanodiscs

被引:31
|
作者
Sun, Chang [1 ,2 ]
Gennis, Robert B. [1 ]
机构
[1] Univ Illinois, Dept Biochem, 600 S Mathews St, Urbana, IL 61801 USA
[2] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97239 USA
关键词
Styrene-maleic acid copolymer; SMA; Nanodisc; Membrane protein; Cryo-EM; Alternative complex III; Multidrug transporter AcrB; Lipid-protein interaction; Triacylated cysteine; MALEIC ACID COPOLYMER; ALTERNATIVE COMPLEX III; MEMBRANE-PROTEINS; FUNCTIONAL RECONSTITUTION; FREE PURIFICATION; INTACT;
D O I
10.1016/j.chemphyslip.2019.03.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Styrene-maleic acid (SMA) copolymers can extract membrane proteins from native membranes along with lipids as nanodiscs. Preparation with SMA is fast, cost-effective, and captures the native protein-lipid interactions. On the other hand, cryo-EM has become increasingly successful and efficient for structural determinations of membrane proteins, with biochemical sample preparation often the bottleneck. Three recent cryo-EM studies on the efflux transporter AcrB and the alternative complex III: cyt c oxidase supercomplex have demonstrated the potential of SMA nanodisc samples to yield high-resolution structure information of membrane proteins.
引用
收藏
页码:114 / 119
页数:6
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