NMR structure of Mistic, a membrane-integrating protein for membrane protein expression

被引:205
作者
Roosild, TP [1 ]
Greenwald, J [1 ]
Vega, M [1 ]
Castronovo, S [1 ]
Riek, R [1 ]
Choe, S [1 ]
机构
[1] Salk Inst Biol Studies, Struct Biol Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1126/science.1106392
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although structure determination of soluble proteins has become routine, our understanding of membrane proteins has been limited by experimental bottlenecks in obtaining both sufficient yields of protein and ordered crystals. Mistic is an unusual Bacillus subtilis integral membrane protein that folds autonomously into the membrane, bypassing the cellular translocon machinery. Using paramagnetic probes, we determined by nuclear magnetic resonance (NMR) spectroscopy that the protein forms a helical bundle with a surprisingly polar lipid-facing surface. Additional experiments suggest that Mistic can be used for high-level production of other membrane proteins in their native conformations, including many eukaryotic proteins that have previously been intractable to bacterial. expression.
引用
收藏
页码:1317 / 1321
页数:5
相关论文
共 25 条
[1]   Structure of outer membrane protein A transmembrane domain by NMR spectroscopy [J].
Arora, A ;
Abildgaard, F ;
Bushweller, JH ;
Tamm, LK .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (04) :334-338
[2]   Crystal structure of Escherichia coli MscS, a voltage-modulated and mechanosensitive channel [J].
Bass, RB ;
Strop, P ;
Barclay, M ;
Rees, DC .
SCIENCE, 2002, 298 (5598) :1582-1587
[3]   Utilization of site-directed spin labeling and high-resolution heteronuclear nuclear magnetic resonance for global fold determination of large proteins with limited nuclear overhauser effect data [J].
Battiste, JL ;
Wagner, G .
BIOCHEMISTRY, 2000, 39 (18) :5355-5365
[4]   THE CRYSTAL-STRUCTURE OF DIPHTHERIA-TOXIN [J].
CHOE, S ;
BENNETT, MJ ;
FUJII, G ;
CURMI, PMG ;
KANTARDJIEFF, KA ;
COLLIER, RJ ;
EISENBERG, D .
NATURE, 1992, 357 (6375) :216-222
[5]  
Clore GM, 1997, NAT STRUCT BIOL, V4, P849
[6]   NMR structure of the integral membrane protein OmpX [J].
Fernández, C ;
Hilty, C ;
Wider, G ;
Güntert, P ;
Wüthrich, K .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 336 (05) :1211-1221
[7]  
Guntert Peter, 2004, Methods Mol Biol, V278, P353
[8]   Membrane protein-lipid interactions in mixed micelles studied by NMR spectroscopy with the use of paramagnetic reagents [J].
Hilty, C ;
Wider, G ;
Fernández, C ;
Wüthrich, K .
CHEMBIOCHEM, 2004, 5 (04) :467-473
[9]   Solution structure and dynamics of the outer membrane enzyme PagP by NMR [J].
Hwang, PM ;
Choy, WY ;
Lo, EI ;
Chen, L ;
Forman-Kay, JD ;
Raetz, CRH ;
Privé, GG ;
Bishop, RE ;
Kay, LE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) :13560-13565
[10]   X-ray structure of a voltage-dependent K+ channel [J].
Jiang, YX ;
Lee, A ;
Chen, JY ;
Ruta, V ;
Cadene, M ;
Chait, BT ;
MacKinnon, R .
NATURE, 2003, 423 (6935) :33-41