Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin.

Abstract:

:In this study terminal cisternae vesicles from rabbit skeletal muscle were fused into planar bilayers and the effect of calmodulin on single Ca2+ release channel currents was investigated. In the presence of 10(-7) and 10(-9) M free [Ca2+], nanomolar concentrations of calmodulin activated the channel by increasing the open probability of single-channel events in a dose dependent manner. The activatory effect of calmodulin was reversed by 10 microM ruthenium red. At 10(-5) M free [Ca2+], calmodulin (0.1-1 microM) inhibited channel activity. Calmodulin overlays were carried out using concentrations of Ca2+ similar to those used for the planar lipid bilayer assays. In the presence of 10(-7) M [Ca2+], calmodulin bound to the ryanodine receptor, to a region defined by residues 2937-3225 and 3546-3655. These results suggest that calmodulin may activate the Ca(2+)-release channel (ryanodine-receptor) by interacting with binding sites localized in the central portion of the RYR protomer.

authors

Buratti R,Prestipino G,Menegazzi P,Treves S,Zorzato F

doi

10.1006/bbrc.1995.2238

subject

Has Abstract

pub_date

1995-08-24 00:00:00

pages

1082-90

issue

3

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(85)72238-3

journal_volume

213

pub_type

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