Signaling within Allosteric Machines: Signal Transmission Pathways Inside G Protein-Coupled Receptors

被引:10
作者
Bartuzi, Damian [1 ]
Kaczor, Agnieszka A. [1 ,2 ]
Matosiuk, Dariusz [1 ]
机构
[1] Med Univ Lublin, Dept Synth & Chem Technol Pharmaceut Subst, Comp Modelling Lab, 4A Chodzki Str, PL-20093 Lublin, Poland
[2] Univ Eastern Finland, Sch Pharm, Yliopistonranta 1,POB 1627, FI-70211 Kuopio, Finland
来源
MOLECULES | 2017年 / 22卷 / 07期
关键词
GPCRs; signaling; allostery; protein dynamics; MU-OPIOID RECEPTOR; ACTIVITY-MODIFYING PROTEINS; CRYSTAL-STRUCTURE; BETA(2)-ADRENERGIC RECEPTOR; ADENOSINE A(2A); BETA-ARRESTIN; CONFORMATIONAL-CHANGES; DYNAMICS SIMULATIONS; MONOMERIC RHODOPSIN; NERVOUS-SYSTEM;
D O I
10.3390/molecules22071188
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
In recent years, our understanding of function of G protein-coupled receptors (GPCRs) has changed from a picture of simple signal relays, transmitting only a particular signal to a particular G protein heterotrimer, to versatile machines, capable of various responses to different stimuli and being modulated by various factors. Some recent reports provide not only the data on ligands / modulators and resultant signals induced by them, but also deeper insights into exact pathways of signal migration and mechanisms of signal transmission through receptor structure. Combination of these computational and experimental data sheds more light on underlying mechanisms of signal transmission and signaling bias in GPCRs. In this review we focus on available clues on allosteric pathways responsible for complex signal processing within GPCRs structures, with particular emphasis on linking compatible in silico-and in vitro-derived data on the most probable allosteric connections.
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页数:24
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