Internal structure and visualization of transmembrane domains of the RyR1 calcium release channel by cryo-EM

Montserrat Samsó, Terence Wagenknecht, P. D. Allen

Research output: Contribution to journalArticle

151 Citations (Scopus)

Abstract

RyR1 is an intracellular calcium channel with a central role in muscle contraction. We obtained a three-dimensional reconstruction of the RyR1 in the closed state at a nominal resolution of ∼10 Å using cryo-EM. The cytoplasmic assembly consists of a series of interconnected tubular structures that merge into four columns that extend into the transmembrane assembly. The transmembrane assembly, which has at least six transmembrane α-helices per monomer, has four tilted rods that can be fitted with the inner helices of a closed K+ channel atomic structure. The rods splay out at the lumenal side and converge into a dense ring at the cytoplasmic side. Another set of four rods emerges from this ring and shapes the inner part of the four columns. The resulting constricted axial structure provides direct continuity between cytoplasmic and transmembrane assemblies, and a possible mechanism for control of channel gating through conformational changes in the cytoplasmic assembly.

Original languageEnglish (US)
Pages (from-to)539-544
Number of pages6
JournalNature Structural and Molecular Biology
Volume12
Issue number6
DOIs
StatePublished - Jun 2005
Externally publishedYes

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Ryanodine Receptor Calcium Release Channel
Calcium Channels
Muscle Contraction

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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Internal structure and visualization of transmembrane domains of the RyR1 calcium release channel by cryo-EM. / Samsó, Montserrat; Wagenknecht, Terence; Allen, P. D.

In: Nature Structural and Molecular Biology, Vol. 12, No. 6, 06.2005, p. 539-544.

Research output: Contribution to journalArticle

Samsó, Montserrat ; Wagenknecht, Terence ; Allen, P. D. / Internal structure and visualization of transmembrane domains of the RyR1 calcium release channel by cryo-EM. In: Nature Structural and Molecular Biology. 2005 ; Vol. 12, No. 6. pp. 539-544.
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