Structural genomics of GPCRs

被引:75
作者
Lundstrom, K [1 ]
机构
[1] BioXtal, CH-1066 Epalinges, Switzerland
关键词
D O I
10.1016/j.tibtech.2004.12.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
G protein-coupled receptors (GPCRs) are targets for 60-70% of drugs in development today. Traditionally, the drug discovery process has relied on screening of chemical compounds to identify novel and more-efficient drug molecules. Structure-based drug design, however, provides a targeted approach but has been severely hampered by limited knowledge of high-resolution structures of GPCRs owing to the difficulties encountered in their expression, purification and crystallization. In addition to individual laboratories studying specific GPCRs, structural genomics initiatives have been established as large networks with a wide range of expertise in protein expression, purification and crystallography. Several of these national and international consortia have included GPCRs in their programs. Milligram quantities of GPCRs can now be expressed in several expression systems and purified to high homogeneity. However, success in crystallization still requires major technological improvement.
引用
收藏
页码:103 / 108
页数:6
相关论文
共 39 条
[1]   The human D1A dopamine receptor:: Heterologous expression in Saccharomyces cerevisiae and purification of the functional receptor [J].
Andersen, B ;
Stevens, RC .
PROTEIN EXPRESSION AND PURIFICATION, 1998, 13 (01) :111-119
[2]   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
[3]  
Bailey WJ, 2001, EXPERT OPIN THER PAT, V11, P1861
[4]   Structure-based analysis of GPCR function:: Conformational adaptation of both agonist and receptor upon leukotriene B4 binding to recombinant BLT1 [J].
Baneres, JL ;
Martin, A ;
Hullot, P ;
Girard, JP ;
Rossi, JC ;
Parello, J .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 329 (04) :801-814
[5]   Molecular tinkering of G protein-coupled receptors: an evolutionary success [J].
Bockaert, J ;
Pin, JP .
EMBO JOURNAL, 1999, 18 (07) :1723-1729
[6]  
DAVIS I, 1997, CHILD WELFARE RES RE, V2, P272
[7]   HIV-1 Entry Cofactor: Functional cDNA Cloing of a Seven-Transmembrane, G protein-Coupled Receptor [J].
Feng, Yu ;
Broder, Christopher C. ;
Kennedy, Paul E. ;
Berger, Edward A. .
JOURNAL OF IMMUNOLOGY, 2011, 186 (11) :872-877
[8]  
FRASER CM, 1989, J BIOL CHEM, V264, P11754
[9]   Uncovering molecular mechanisms involved in activation of G protein-coupled receptors [J].
Gether, U .
ENDOCRINE REVIEWS, 2000, 21 (01) :90-113
[10]   Adenovirus vectors for high-efficiency gene transfer into mammalian cells [J].
Graham, FL .
IMMUNOLOGY TODAY, 2000, 21 (09) :426-428