药效团
G蛋白偶联受体
受体
突变
化学
生物化学
立体化学
计算生物学
机制(生物学)
生物
基因
突变
哲学
认识论
作者
Lucky Ahmed,Yuetian Zhang,Eric Block,Michael Buehl,Michael J. Corr,Rodrigo A. Cormanich,Sivaji Gundala,Hiroaki Matsunami,David O′Hagan,Mehmet Özbil,Yi Pan,Sivakumar Sekharan,Nicholas S. Ten,Mingan Wang,Mingyan Yang,Qingzhi Zhang,Ruina Zhang,Víctor S. Batista,Hanyi Zhuang
标识
DOI:10.1073/pnas.1713026115
摘要
Significance While natural musk has been used for 2,000 years in perfumery, and in traditional medicine for its cardioprotective effects, its mode of activating odorant receptors (ORs) is unknown. ORs, G protein-coupled receptors (GPCRs), which constitute 40% of all pharmacophore receptors, are also expressed in nonolfactory tissues. Understanding the activation of ORs at the molecular level is challenging due to lack of crystallographic models. By combining site-directed mutagenesis with computational studies of human musk ORs involving 35 chiral and achiral muscone analogues, we propose structural models, including binding site prediction and responsible amino acid residues identification. Our studies of musk-responsive ORs should assist the study of the pharmacological effects of musks involving non-OR GPCRs.
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