| Literature DB >> 27726881 |
Jin Xiang1, Eugene Chun2, Chang Liu2, Liang Jing2, Zina Al-Sahouri2, Lan Zhu2, Wei Liu3.
Abstract
G protein-coupled receptors (GPCRs) constitute the largest class of drug targets in the human genome, which highlights the importance of understanding the molecular basis of their activation, downstream signaling, and regulation. Since 2007, great progress has been made in the field of GPCR structure determination and their signaling complexes at the molecular level. Here, we summarize the high-resolution structures of over 30 different GPCRs with their co-crystallized ligands, and outline the successful strategies involved, including construct design, expression systems, and lipidic cubic phase (LCP) composition, and the many key technical parameters of the crystallization methods. By comparing the success rates of different strategies used in the past, we wish to pave the road for more successful structure-function research for GPCRs in the future.Entities:
Keywords: GPCRs; ligand binding; lipidic cubic phase; protein engineering; structure-based drug discovery
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Year: 2016 PMID: 27726881 DOI: 10.1016/j.tips.2016.09.009
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819