G-protein βγ subunits as multi-functional scaffolds and transducers in G-protein-coupled receptor signaling

被引:52
作者
Smrcka, Alan V. [1 ]
Fisher, Isaac [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48104 USA
[2] Univ Rochester, Sch Med, Dept Physiol & Pharmacol, Rochester, NY 14629 USA
基金
美国国家卫生研究院;
关键词
G protein; G-protein-coupled receptor; WD-40 repeat proteins; Signal transduction; Membrane interactions; Translocation; Second messengers; Cyclic AMP; Phosphatidylinositol; Adenylate cyclase; G-protein-coupled receptor kinase; Phospholipase C; 3-kinase; CRYO-EM STRUCTURE; PHOSPHOINOSITIDE; 3-KINASE; CRYSTAL-STRUCTURE; AMINO-TERMINUS; NUCLEOTIDE EXCHANGE; STRUCTURAL BASIS; PLASMA-MEMBRANE; MOLECULAR-BASIS; GLP-1; RECEPTOR; WD-REPEAT;
D O I
10.1007/s00018-019-03275-2
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
G-protein beta gamma subunits are key participants in G-protein signaling. These subunits facilitate interactions between receptors and G proteins that are critical for the G protein activation cycle at the plasma membrane. In addition, they play roles in directly transducing signals to an ever expanding range of downstream targets, including integral membrane and cytosolic proteins. Emerging data indicate that G beta gamma may play additional roles at intracellular compartments including endosomes, the Golgi apparatus, and the nucleus. Here, we discuss the molecular and structural basis for their ability to coordinate this wide range of cellular activities.
引用
收藏
页码:4447 / 4459
页数:13
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