Successful Strategies to Determine High-Resolution Structures of GPCRs

Jin Xiang, Eugene Chun, Chang Liu, Liang Jing, Zina Al-Sahouri, Lan Zhu, Wei Liu

Research output: Contribution to journalReview articlepeer-review

52 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)1055-1069
Number of pages15
JournalTrends in Pharmacological Sciences
Issue number12
StatePublished - Dec 1 2016


  • GPCRs
  • ligand binding
  • lipidic cubic phase
  • protein engineering
  • structure-based drug discovery

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology


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