Recent advances in computational studies of GPCR-G protein interactions

被引:11
|
作者
Wang, Jinan [1 ,2 ]
Miao, Yinglong [1 ,2 ]
机构
[1] Univ Kansas, Ctr Computat Biol, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
来源
关键词
2ND INTRACELLULAR LOOP; MOLECULAR-DYNAMICS SIMULATIONS; CRYO-EM STRUCTURE; BETA(2) ADRENERGIC-RECEPTOR; STABILIZED ACTIVE STATE; COUPLED RECEPTOR; STRUCTURAL DETERMINANTS; NUCLEOTIDE EXCHANGE; MUSCARINIC RECEPTOR; CRYSTAL-STRUCTURE;
D O I
10.1016/bs.apcsb.2018.11.011
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
Protein-protein interactions are key in cellular signaling. G protein-coupled receptors (GPCRs), the largest superfamily of human membrane proteins, are able to transduce extracellular signals (e.g., hormones and neurotransmitters) to intracellular proteins, in particular the G proteins. Since GPCRs serve as primary targets of similar to 1/3 of currently marketed drugs, it is important to understand mechanisms of GPCR signaling in order to design selective and potent drug molecules. This chapter focuses on recent advances in computational studies of the GPCR-G protein interactions using bioinformatics, protein-protein docking and molecular dynamics simulation approaches.
引用
收藏
页码:397 / 419
页数:23
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