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螺旋和β桶状膜蛋白与去污剂相关的溶液构象。

Detergent-associated solution conformations of helical and beta-barrel membrane proteins.

作者信息

Mo Yiming, Lee Byung-Kwon, Ankner John F, Becker Jeffrey M, Heller William T

机构信息

Center for Structural Molecular Biology, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.

出版信息

J Phys Chem B. 2008 Oct 23;112(42):13349-54. doi: 10.1021/jp801266r. Epub 2008 Sep 25.

Abstract

Membrane proteins present major challenges for structural biology. In particular, the production of suitable crystals for high-resolution structural determination continues to be a significant roadblock for developing an atomic-level understanding of these vital cellular systems. The use of detergents for extracting membrane proteins from the native membrane for either crystallization or reconstitution into model lipid membranes for further study is assumed to leave the protein with the proper fold with a belt of detergent encompassing the membrane-spanning segments of the structure. Small-angle X-ray scattering was used to probe the detergent-associated solution conformations of three membrane proteins, namely bacteriorhodopsin (BR), the Ste2p G-protein coupled receptor from Saccharomyces cerevisiae, and the Escherichia coli porin OmpF. The results demonstrate that, contrary to the traditional model of a detergent-associated membrane protein, the helical proteins BR and Ste2p are not in the expected, compact conformation and associated with detergent micelles, while the beta-barrel OmpF is indeed embedded in a disk-like micelle in a properly folded state. The comparison provided by the BR and Ste2p, both members of the 7TM family of helical membrane proteins, further suggests that the interhelical interactions between the transmembrane helices of the two proteins differ, such that BR, like other rhodopsins, can properly refold to crystallize, while Ste2p continues to prove resistant to crystallization from an initially detergent-associated state.

摘要

膜蛋白给结构生物学带来了重大挑战。特别是,为高分辨率结构测定制备合适的晶体仍然是深入了解这些重要细胞系统原子水平结构的重大障碍。使用去污剂从天然膜中提取膜蛋白用于结晶或重构成模型脂质膜进行进一步研究时,假定蛋白质具有正确的折叠结构,其跨膜片段周围环绕着一层去污剂。小角X射线散射被用于探测三种膜蛋白(即细菌视紫红质(BR)、酿酒酵母的Ste2p G蛋白偶联受体和大肠杆菌孔蛋白OmpF)与去污剂相关的溶液构象。结果表明,与传统的去污剂相关膜蛋白模型相反,螺旋蛋白BR和Ste2p并非处于预期的紧密构象且与去污剂胶束相关,而β桶状的OmpF确实以正确折叠的状态嵌入盘状胶束中。BR和Ste2p都是螺旋膜蛋白7TM家族的成员,它们之间的比较进一步表明,这两种蛋白跨膜螺旋之间的螺旋间相互作用存在差异,因此BR像其他视紫红质一样,可以正确重折叠以进行结晶,而Ste2p从最初与去污剂相关的状态开始就一直难以结晶。

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1
High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor.
Science. 2007 Nov 23;318(5854):1258-65. doi: 10.1126/science.1150577. Epub 2007 Oct 25.
2
GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function.
Science. 2007 Nov 23;318(5854):1266-73. doi: 10.1126/science.1150609. Epub 2007 Oct 25.
3
Crystal structure of the human beta2 adrenergic G-protein-coupled receptor.
Nature. 2007 Nov 15;450(7168):383-7. doi: 10.1038/nature06325. Epub 2007 Oct 21.
4
Size and shape of detergent micelles determined by small-angle X-ray scattering.
J Phys Chem B. 2007 Nov 1;111(43):12427-38. doi: 10.1021/jp073016l. Epub 2007 Oct 9.
5
Investigation of the conformational states of Wzz and the Wzz.O-antigen complex under near-physiological conditions.
Biochemistry. 2007 Oct 23;46(42):11744-52. doi: 10.1021/bi701181r. Epub 2007 Sep 27.
6
Affinity purification and characterization of a G-protein coupled receptor, Saccharomyces cerevisiae Ste2p.
Protein Expr Purif. 2007 Nov;56(1):62-71. doi: 10.1016/j.pep.2007.06.002. Epub 2007 Jun 20.
7
Small-angle X-ray scattering study of photosystem I-detergent complexes: implications for membrane protein crystallization.
J Phys Chem B. 2007 Apr 26;111(16):4211-9. doi: 10.1021/jp067463x. Epub 2007 Mar 29.
8
Self-assembled colloidal crystals from ZrO2 nanoparticles.
J Phys Chem B. 2006 Oct 5;110(39):19456-60. doi: 10.1021/jp062471z.

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