What's for lunch at the conformational cafeteria?

被引:16
作者
Clarke, WP [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Pharmacol, San Antonio, TX 78229 USA
关键词
D O I
10.1124/mol.105.013060
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this issue of Molecular Pharmacology, Mukhopadhyay and Howlett present evidence for ligand-selective conformations of the CB1 cannabinoid receptor with differential coupling to G proteins. Ligand-directed signaling to different cellular effector pathways extends drug selectivity beyond that afforded by differential affinity for different receptor subtypes. The challenge for pharmacologists of the future will be not only to identify ligand-selective receptor conformations but also to develop an understanding of the relationships between those conformations, cell function, and ultimately therapeutics. As we learn more about ligand-selective receptor conformations, it should be possible to develop response-selective drugs that maximize therapeutic efficacy and minimize unwanted effects.
引用
收藏
页码:1819 / 1821
页数:3
相关论文
共 32 条
[1]   RNA-editing of the 5-HT2C receptor alters agonist-receptor-effector coupling specificity [J].
Berg, KA ;
Cropper, JD ;
Niswender, CM ;
Sanders-Bush, E ;
Emeson, RB ;
Clarke, WP .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (02) :386-392
[2]   Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: Evidence for agonist-directed trafficking of receptor stimulus [J].
Berg, KA ;
Maayani, S ;
Goldfarb, J ;
Scaramellini, C ;
Leff, P ;
Clarke, WP .
MOLECULAR PHARMACOLOGY, 1998, 54 (01) :94-104
[3]   Differential opioid agonist regulation of the mouse mu opioid receptor [J].
Blake, AD ;
Bot, G ;
Freeman, JC ;
Reisine, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) :782-790
[4]  
Bonhaus DW, 1998, J PHARMACOL EXP THER, V287, P884
[5]  
Chakrabarti S, 1998, J NEUROCHEM, V71, P231
[6]   The elusive nature of intrinsic efficacy [J].
Clarke, WP ;
Bond, RA .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (07) :270-276
[7]   A fluorescent probe designed for studying protein conformational change [J].
Cohen, BE ;
Pralle, A ;
Yao, XJ ;
Swaminath, G ;
Gandhi, CS ;
Jan, YN ;
Kobilka, BK ;
Isacoff, EY ;
Jan, LY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (04) :965-970
[8]   Influence of receptor number on functional responses elicited by agonists acting at the human adenosine A1 receptor:: Evidence for signaling pathway-dependent changes in agonist potency and relative intrinsic activity [J].
Cordeaux, Y ;
Briddon, SJ ;
Megson, AE ;
McDonnell, J ;
Dickenson, JM ;
Hill, SJ .
MOLECULAR PHARMACOLOGY, 2000, 58 (05) :1075-1084
[9]  
Furchgott R., 1966, ADV DRUG RES, V3, P21
[10]   Functionally different agonists induce distinct conformations in the G protein coupling domain of the β2 adrenergic receptor [J].
Ghanouni, P ;
Gryczynski, Z ;
Steenhuis, JJ ;
Lee, TW ;
Farrens, DL ;
Lakowicz, JR ;
Kobilka, BK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) :24433-24436