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Structure of IP3R channel: high-resolution insights from cryo-EM.
Baker, Mariah R; Fan, Guizhen; Serysheva, Irina I.
Affiliation
  • Baker MR; Structural Biology Imaging Center, Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, 6431 Fannin Street, Houston, TX 77030, USA.
  • Fan G; Structural Biology Imaging Center, Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, 6431 Fannin Street, Houston, TX 77030, USA.
  • Serysheva II; Structural Biology Imaging Center, Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, 6431 Fannin Street, Houston, TX 77030, USA. Electronic address: irina.i.serysheva@uth.tmc.edu.
Curr Opin Struct Biol ; 46: 38-47, 2017 10.
Article in En | MEDLINE | ID: mdl-28618351
ABSTRACT
Inositol 1,4,5-trisphosphate receptors (IP3Rs) are ubiquitously expressed intracellular Ca2+ channels and the major mediators of cellular Ca2+ signals generated by the release of Ca2+ ions from intracellular stores in response to a variety of extracellular stimuli. Despite established physiological significance and proven involvements of IP3R channels in many human diseases, detailed structural basis for signal detection by these ion channels and their gating remain obscure. Recently, single particle electron cryomicroscopy (cryo-EM) has yielded a long-awaited near-atomic resolution structure of the entire full-length type 1 IP3R. This structure provided exciting mechanistic insights into the molecular assembly of IP3R, revealing the pronounced structural conservation of Ca2+ release channels and raising many fundamental and controversial questions on their activation and gating. Here we summarize the major technological advances that propelled our cryo-EM analysis of IP3R to near-atomic resolution and discuss what the future holds for structural biology of Ca2+ release channels.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cryoelectron Microscopy / Inositol 1,4,5-Trisphosphate Receptors Limits: Animals / Humans Language: En Journal: Curr Opin Struct Biol Journal subject: BIOLOGIA MOLECULAR Year: 2017 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cryoelectron Microscopy / Inositol 1,4,5-Trisphosphate Receptors Limits: Animals / Humans Language: En Journal: Curr Opin Struct Biol Journal subject: BIOLOGIA MOLECULAR Year: 2017 Document type: Article Affiliation country: United States
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