Editors' ChoiceStructural Biology

GPCR Close-Up

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Science Signaling  17 Jul 2012:
Vol. 5, Issue 233, pp. ec191
DOI: 10.1126/scisignal.2003394

Structures of G protein–coupled receptors (GPCRs), determined in the past few years, have provided insight into the function of this important family of membrane proteins. Liu et al. used a protein-engineering strategy to produce a stabilized version of the human A2A adenosine receptor (A2AAR). The high-resolution structure reveals the position of about 60 internal waters, which suggests an almost continuous channel in the GPCR and can explain the allosteric effects of Na+ on ligand binding and how cholesterol may contribute to GPCR stabilization.

W. Liu, E. Chun, A. A. Thompson, P. Chubukov, F. Xu, V. Katritch, G. W. Han, C. B. Roth, L. H. Heitman, A. P. IJzerman, V. Cherezov, R. C. Stevens, Structural basis for allosteric regulation of GPCRs by sodium ions. Science 337, 232–236 (2012). [Abstract] [Full Text]

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