Arrestin interaction with rhodopsin - Conceptual models

被引:33
作者
Modzelewska, Anna
Filipek, Slawomir [1 ]
Palczewski, Krzysztof
Park, Paul S. -H.
机构
[1] Int Inst Mol & Cell Biol, PL-02109 Warsaw, Poland
[2] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
G protein-coupled receptor; arrestin; oligomerization; signal transduction; G protein;
D O I
10.1385/CBB:46:1:1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is becoming increasingly apparent that G protein-coupled receptors (GPCRs) can exist and function as oligomers. This notion differs from the classical view of signaling wherein the receptor has been presumed to be monomeric. Despite this shift in views, the interpretation of data related to GPCR function is still largely carried out within the framework of a monomeric receptor. Rhodopsin is a prototypical GPCR that initiates phototransduction. Like other GPCRs, the activity of rhodopsin is regulated by phosphorylation and the binding of arrestin. In the current investigation, we have explored by modeling methods the interaction of rhodopsin and arrestin under the assumption that either one or two rhodopsin molecules bind each arrestin molecule. The dimeric receptor framework may provide a more accurate representation of the system and is therefore likely to lead to a better and more accurate understanding of GPCR signaling.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 85 条
[51]   Paired activation of two components within muscarinic M3 receptor dimers is required for recruitment of β-arrestin-1 to the plasma membrane [J].
Novi, F ;
Stanasila, L ;
Giorgi, F ;
Corsini, GU ;
Cotecchia, S ;
Maggio, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (20) :19768-19776
[52]   RHODOPSIN PHOSPHORYLATION AND DEPHOSPHORYLATION IN-VIVO [J].
OHGURO, H ;
VANHOOSER, JP ;
MILAM, AH ;
PALCZEWSKI, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14259-14262
[53]   CONTROL OF RHODOPSIN MULTIPLE PHOSPHORYLATION [J].
OHGURO, H ;
JOHNSON, RS ;
ERICSSON, LH ;
WALSH, KA ;
PALCZEWSKI, K .
BIOCHEMISTRY, 1994, 33 (04) :1023-1028
[54]   The retinal conformation and its environment in rhodopsin in light of a new 2.2 Å crystal structure [J].
Okada, T ;
Sugihara, M ;
Bondar, AN ;
Elstner, M ;
Entel, P ;
Buss, V .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 342 (02) :571-583
[55]   Activation of rhodopsin: new insights from structural and biochemical studies [J].
Okada, T ;
Ernst, OP ;
Palczewski, K ;
Hofmann, KP .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (05) :318-324
[56]  
PALCZEWSKI K, 1994, PROTEIN SCI, V3, P314
[57]   Crystal structure of rhodopsin: A G protein-coupled receptor [J].
Palczewski, K ;
Kumasaka, T ;
Hori, T ;
Behnke, CA ;
Motoshima, H ;
Fox, BA ;
Le Trong, I ;
Teller, DC ;
Okada, T ;
Stenkamp, RE ;
Yamamoto, M ;
Miyano, M .
SCIENCE, 2000, 289 (5480) :739-745
[58]  
PALCZEWSKI K, 1991, J BIOL CHEM, V266, P18649
[59]  
PALCZEWSKI K, 1991, J BIOL CHEM, V266, P15334
[60]   MASS-SPECTROMETRIC IDENTIFICATION OF PHOSPHORYLATION SITES IN BLEACHED BOVINE RHODOPSIN [J].
PAPAC, DI ;
OATIS, JE ;
CROUCH, RK ;
KNAPP, DR .
BIOCHEMISTRY, 1993, 32 (23) :5930-5934