Structural highlights
Publication Abstract from PubMed
Single particle cryogenic-electron microscopy (cryo-EM) is used extensively to determine structures of activated G protein-coupled receptors (GPCRs) in complex with G proteins or arrestins. However, applying it to GPCRs without signaling proteins remains challenging because most receptors lack structural features in their soluble domains to facilitate image alignment. In GPCR crystallography, inserting a fusion protein between transmembrane helices 5 and 6 is a highly successful strategy for crystallization. Although a similar strategy has the potential to broadly facilitate cryo-EM structure determination of GPCRs alone without signaling protein, the critical determinants that make this approach successful are not yet clear. Here, we address this shortcoming by exploring different fusion protein designs, which lead to structures of antagonist bound A(2A) adenosine receptor at 3.4 A resolution and unliganded Smoothened at 3.7 A resolution. The fusion strategies explored here are likely applicable to cryo-EM interrogation of other GPCRs and small integral membrane proteins.
Fusion protein strategies for cryo-EM study of G protein-coupled receptors.,Zhang K, Wu H, Hoppe N, Manglik A, Cheng Y Nat Commun. 2022 Jul 28;13(1):4366. doi: 10.1038/s41467-022-32125-2. PMID:35902590[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Zhang K, Wu H, Hoppe N, Manglik A, Cheng Y. Fusion protein strategies for cryo-EM study of G protein-coupled receptors. Nat Commun. 2022 Jul 28;13(1):4366. PMID:35902590 doi:10.1038/s41467-022-32125-2
