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Original Article

^a Cardiovascular Research Group, University of Calgary, Calgary, Alberta, Canada T2N 4N1
^b Department of Physiology and Biophysics, University of Calgary, Calgary, Alberta, Canada T2N 4N1
^c Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta, Canada T2N 4N1
Department of Physiology and Biophysics, University of Calgary, 330 Hospital Drive NW, Calgary, Alberta T2N 4N1, Canada.(403) 283-4841

swchen{at}ucalgary.ca

Activation of the cardiac ryanodine receptor (RyR2) by Ca²+ is an essential step in excitation-contraction coupling in heart muscle. However, little is known about the molecular basis of activation of RyR2 by Ca²+. In this study, we investigated the role in Ca²+ sensing of the conserved glutamate 3987 located in the predicted transmembrane segment M2 of the mouse RyR2. Single point mutation of this conserved glutamate to alanine (E3987A) reduced markedly the sensitivity of the channel to activation by Ca²+, as measured by using single-channel recordings in planar lipid bilayers and by [³H]ryanodine binding assay. However, this mutation did not alter the affinity of [³H]ryanodine binding and the single-channel conductance. In addition, the E3987A mutant channel was activated by caffeine and ATP, was inhibited by Mg²+, and was modified by ryanodine in a fashion similar to that of the wild-type channel. Coexpression of the wild-type and mutant E3987A RyR2 proteins in HEK293 cells produced individual single channels with intermediate sensitivities to activating Ca²+. These results are consistent with the view that glutamate 3987 is a major determinant of Ca²+ sensitivity to activation of the mouse RyR2 channel, and that Ca²+ sensing by RyR2 involves the cooperative action between ryanodine receptor monomers. The results of this study also provide initial insights into the structural and functional properties of the mouse RyR2, which should be useful for studying RyR2 function and regulation in genetically modified mouse models.

Key Words: excitation-contraction coupling • Ca²+-induced Ca²+ release • Ca²+ sensing • sarcoplasmic reticulum • planar lipid bilayers

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