High capacity in G protein-coupled receptor signaling

被引:37
作者
Keshelava, Amiran [1 ]
Solis, Gonzalo P. [1 ]
Hersch, Micha [2 ,3 ]
Koval, Alexey [1 ]
Kryuchkov, Mikhail [1 ]
Bergmann, Sven [2 ,3 ,4 ]
Katanaev, Vladimir L. [1 ,5 ]
机构
[1] Univ Lausanne, Fac Biol & Med, Dept Pharmacol & Toxicol, CH-1011 Lausanne, Switzerland
[2] Univ Lausanne, Fac Biol & Med, Dept Computat Biol, CH-1011 Lausanne, Switzerland
[3] Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
[4] Univ Cape Town, Dept Integrat Biomed Sci, ZA-7925 Cape Town, South Africa
[5] Far Eastern Fed Univ, Sch Biomed, Vladivostok 690922, Russia
基金
瑞士国家科学基金会;
关键词
MUSCARINIC ACETYLCHOLINE-RECEPTORS; INFORMATION-TRANSMISSION; TRANSDUCTION; SUPPRESSION; HOMEOSTASIS; RGS;
D O I
10.1038/s41467-018-02868-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
G protein-coupled receptors (GPCRs) constitute a large family of receptors that activate intracellular signaling pathways upon detecting specific extracellular ligands. While many aspects of GPCR signaling have been uncovered through decades of studies, some fundamental properties, like its channel capacity-a measure of how much information a given transmission system can reliably transduce-are still debated. Previous studies concluded that GPCRs in individual cells could transmit around one bit of information about the concentration of the ligands, allowing only for a reliable on or off response. Using muscarinic receptor-induced calcium response measured in individual cells upon repeated stimulation, we show that GPCR signaling systems possess a significantly higher capacity. We estimate the channel capacity of this system to be above two, implying that at least four concentration levels of the agonist can be distinguished reliably. These findings shed light on the basic principles of GPCR signaling.
引用
收藏
页数:8
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