Influences of Membrane Mimetic Environments on Membrane Protein Structures

被引:213
作者
Zhou, Huan-Xiang [1 ,2 ]
Cross, Timothy A. [1 ,3 ,4 ]
机构
[1] Florida State Univ, Inst Mol Biophys, Tallahassee, FL 32310 USA
[2] Florida State Univ, Dept Phys, Tallahassee, FL 32310 USA
[3] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32310 USA
[4] Florida State Univ, Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 42 | 2013年 / 42卷
关键词
structure determination; membrane biophysical properties; structural perturbations; bilayer and detergent environments; native structures; structural enhancement; M2 PROTON CHANNEL; CRYSTAL-STRUCTURE; LIPID-BILAYER; PHOSPHOLAMBAN PENTAMER; MOLECULAR-MECHANISM; DETERGENT MICELLES; COAT PROTEIN; TRANSMEMBRANE; TRANSPORTER; STATE;
D O I
10.1146/annurev-biophys-083012-130326
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The number of membrane protein structures in the Protein Data Bank is becoming significant and growing. Here, the transmembrane domain structures of the helical membrane proteins are evaluated to assess the influences of the membrane mimetic environments. Toward this goal, many of the biophysical properties of membranes are discussed and contrasted with those of the membrane mimetics commonly used for structure determination. Although the mimetic environments can perturb the protein structures to an extent that potentially gives rise to misinterpretation of functional mechanisms, there are also many structures that have a native-like appearance. From this assessment, an initial set of guidelines is proposed for distinguishing native-like from nonnative-like membrane protein structures. With experimental techniques for validation and computational methods for refinement and quality assessment and enhancement, there are good prospects for achieving native-like structures for these very important proteins.
引用
收藏
页码:361 / 392
页数:32
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