G-protein-coupled receptor structures were not built in a day

被引:22
作者
Blois, Tracy M. [1 ]
Bowie, James U. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, UCLA DOE Inst Genom & Prote, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
membrane protein; crystallization; expression; bicells; lipid cubic phase; X-RAY-STRUCTURE; CRYSTALLIZING MEMBRANE-PROTEINS; 2.3 ANGSTROM RESOLUTION; LIPIDIC CUBIC PHASES; CELL-FREE PRODUCTION; ESCHERICHIA-COLI; LACTOSE PERMEASE; FUSION PROTEINS; EXPRESSION; CHANNEL;
D O I
10.1002/pro.165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Among the most exciting recent developments in structural biology is the structure determination of G-protein-coupled receptors (GPCRs), which comprise the largest class of membrane proteins in mammalian cells and have enormous importance for disease and drug development. The GPCR structures are perhaps the most visible examples of a nascent revolution in membrane protein structure determination. Like other major milestones in science, however, such as the sequencing of the human genome, these achievements were built on a hidden foundation of technological developments. Here, we describe some of the methods that are fueling the membrane protein structure revolution and have enabled the determination of the current GPCR structures, along with new techniques that may lead to future structures.
引用
收藏
页码:1335 / 1342
页数:8
相关论文
共 69 条
[1]
Structure and mechanism of the lactose permease of Escherichia coli [J].
Abramson, J ;
Smirnova, I ;
Kasho, V ;
Verner, G ;
Kaback, HR ;
Iwata, S .
SCIENCE, 2003, 301 (5633) :610-615
[2]
MUTATIONAL ANALYSIS OF LIGAND-BINDING ACTIVITY OF BETA-2 ADRENERGIC-RECEPTOR EXPRESSED IN ESCHERICHIA-COLI [J].
BREYER, RM ;
STROSBERG, AD ;
GUILLET, JG .
EMBO JOURNAL, 1990, 9 (09) :2679-2684
[3]
CAFFREY M, 2008, ANN REV BIO IN PRESS
[4]
X-ray structure of EmrE supports dual topology model [J].
Chen, Yen-Ju ;
Pornillos, Owen ;
Lieu, Samantha ;
Ma, Che ;
Chen, Andy P. ;
Chang, Geoffrey .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (48) :18999-19004
[5]
Room to move: Crystallizing membrane proteins in swollen lipidic mesophases [J].
Cherezov, V ;
Clogston, J ;
Papiz, MZ ;
Caffrey, M .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 357 (05) :1605-1618
[6]
A robotic system for crystallizing membrane and soluble proteins in lipidic mesophases [J].
Cherezov, V ;
Peddi, A ;
Muthusubramaniam, L ;
Zheng, YF ;
Caffrey, M .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 :1795-1807
[7]
High-resolution crystal structure of an engineered human β2-adrenergic G protein-coupled receptor [J].
Cherezov, Vadim ;
Rosenbaum, Daniel M. ;
Hanson, Michael A. ;
Rasmussen, Soren G. F. ;
Thian, Foon Sun ;
Kobilka, Tong Sun ;
Choi, Hee-Jung ;
Kuhn, Peter ;
Weis, William I. ;
Kobilka, Brian K. ;
Stevens, Raymond C. .
SCIENCE, 2007, 318 (5854) :1258-1265
[8]
Davidson Alan R., 2006, V340, P171
[9]
A monoclonal antibody for G protein-coupled receptor crystallography [J].
Day, Peter W. ;
Rasmussen, Soren G. F. ;
Parnot, Charles ;
Fung, Juan Jose ;
Masood, Asna ;
Kobilka, Tong Sun ;
Yao, Xiao-Jie ;
Choi, Hee-Jung ;
Weis, William I. ;
Rohrer, Daniel K. ;
Kobilka, Brian K. .
NATURE METHODS, 2007, 4 (11) :927-929
[10]
3-DIMENSIONAL STRUCTURE OF THE PLATELET INTEGRIN RECOGNITION SEGMENT OF THE FIBRINOGEN GAMMA-CHAIN OBTAINED BY CARRIER PROTEIN-DRIVEN CRYSTALLIZATION [J].
DONAHUE, JP ;
PATEL, H ;
ANDERSON, WF ;
HAWIGER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12178-12182