Myoplasmic resting Ca2+ regulation by ryanodine receptors is under the control of a novel Ca2+-binding region of the receptor

Yanyi Chen, Shenghui Xue, Juan Zou, Jose R. Lopez, Jenny J. Yang, Claudio F. Perez

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


Passive SR (sarcoplasmic reticulum) Ca2+ leak through the RyR (ryanodine receptor) plays a critical role in the mechanisms that regulate [Ca2+]rest (intracellular resting myoplasmic free Ca2+ concentration) in muscle. This process appears to be isoform-specific as expression of either RyR1 or RyR3 confers on myotubes different [Ca 2+]rest. Using chimaeric RyR3-RyR1 receptors expressed in dyspedic myotubes, we show that isoformdependent regulation of [Ca2+]rest is primarily defined by a small region of the receptor encompassing amino acids 3770- 4007 of RyR1 (amino acids 3620-3859 of RyR3) named as the CLR (Ca 2+ leak regulatory) region. [Ca2+]rest regulation by the CLR region was associated with alteration of RyRs' Ca2+-activation profile and changes in SR Ca2+-leak rates. Biochemical analysis using Tb3+-binding assays and intrinsic tryptophan fluorescence spectroscopy of purified CLR domains revealed that this determinant of RyRs holds a novel Ca2+-binding domainwith conformational properties that are distinctive to each isoform. Our data suggest that the CLR region provides channels with unique functional properties that modulate the rate of passive SR Ca2+ leak and confer on RyR1 and RyR3 distinctive [Ca 2+]rest regulatory properties. The identification of a new Ca 2+-binding domain ofRyRswith a key modulatory role in [Ca 2+]rest regulation provides new insights into Ca2+- mediated regulation of RyRs.

Original languageEnglish (US)
Pages (from-to)261-271
Number of pages11
JournalBiochemical Journal
Issue number2
StatePublished - Jun 1 2014


  • Calcium leak
  • Calcium-binding site
  • Myotube
  • Skeletal muscle
  • Terbium fluorescence
  • Tryptophan fluorescence

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology
  • Medicine(all)


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