Gut hormone GPCRs: structure, function, drug discovery

Curr Opin Pharmacol. 2016 Dec:31:63-67. doi: 10.1016/j.coph.2016.09.001. Epub 2016 Sep 16.

Abstract

Crystallization and determination of the high resolution three-dimensional structure of the β2-adrenergic receptor in 2007 was followed by structure elucidation of a number of other receptors, including those for neurotensin and glucagon. These major advances foster the understanding of structure-activity relationship of these receptors and structure-based rational design of new ligands having more predictable activity. At present, structure determination of gut hormone receptors in complex with their ligands (natural, synthetic) and interacting signalling proteins, for example, G-proteins, arrestins, represents a challenge which promises to revolutionize gut hormone endocrinonology.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arrestins / metabolism
  • Crystallization
  • Drug Design
  • Drug Discovery / methods*
  • GTP-Binding Proteins / metabolism
  • Gastrointestinal Hormones / metabolism*
  • Humans
  • Ligands
  • Receptors, Adrenergic, beta-2 / chemistry
  • Receptors, Adrenergic, beta-2 / metabolism
  • Receptors, G-Protein-Coupled / chemistry
  • Receptors, G-Protein-Coupled / metabolism*
  • Structure-Activity Relationship

Substances

  • Arrestins
  • Gastrointestinal Hormones
  • Ligands
  • Receptors, Adrenergic, beta-2
  • Receptors, G-Protein-Coupled
  • GTP-Binding Proteins