DP4 is a 36-residue synthetic peptide that corresponds to the Leu2442-Pro2477 region of RyR1 that contains the reported malignant hyperthermia (MH) mutation site. It has been proposed that DP4 disrupts the normal interdomain interactions that stabilize the closed state of the Ca2+ release channel (Yamamoto, T., R. El-Hayek, and N. Ikemoto. 2000. J. Biol. Chem. 275:11618–11625). We have investigated the effects of DP4 on local SR Ca2+ release events (Ca2+ sparks) in saponin-permeabilized frog skeletal muscle fibers using laser scanning confocal microscopy (line-scan mode, 2 ms/line), as well as the effects of DP4 on frog SR vesicles and frog single RyR Ca2+ release channels reconstituted in planar lipid bilayers. DP4 caused a significant increase in Ca2+ spark frequency in muscle fibers. However, the mean values of the amplitude, rise time, spatial half width, and temporal half duration of the Ca2+ sparks, as well as the distribution of these parameters, remained essentially unchanged in the presence of DP4. Thus, DP4 increased the opening rate, but not the open time of the RyR Ca2+ release channel(s) generating the sparks. DP4 also increased [3H]ryanodine binding to SR vesicles isolated from frog and mammalian skeletal muscle, and increased the open probability of frog RyR Ca2+ release channels reconstituted in bilayers, without changing the amplitude of the current through those channels. However, unlike in Ca2+ spark experiments, DP4 produced a pronounced increase in the open time of channels in bilayers. The same peptide with an Arg17 to Cys17 replacement (DP4mut), which corresponds to the Arg2458-to-Cys2458 mutation in MH, did not produce a significant effect on RyR activation in muscle fibers, bilayers, or SR vesicles. Mg2+ dependence experiments conducted with permeabilized muscle fibers indicate that DP4 preferentially binds to partially Mg2+-free RyR(s), thus promoting channel opening and production of Ca2+ sparks.
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1 January 2002
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December 17 2001
Interdomain Interactions within Ryanodine Receptors Regulate Ca2+ Spark Frequency in Skeletal Muscle
Alexander Shtifman,
Alexander Shtifman
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
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Christopher W. Ward,
Christopher W. Ward
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
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Takeshi Yamamoto,
Takeshi Yamamoto
bBoston Biomedical Research Institute, Department of Muscle Research, Watertown, MA 02472
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Jianli Wang,
Jianli Wang
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
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Beth Olbinski,
Beth Olbinski
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
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Hector H. Valdivia,
Hector H. Valdivia
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
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Noriaki Ikemoto,
Noriaki Ikemoto
bBoston Biomedical Research Institute, Department of Muscle Research, Watertown, MA 02472
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Martin F. Schneider
Martin F. Schneider
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
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Alexander Shtifman
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
Christopher W. Ward
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
Takeshi Yamamoto
bBoston Biomedical Research Institute, Department of Muscle Research, Watertown, MA 02472
Jianli Wang
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
Beth Olbinski
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
Hector H. Valdivia
cUniversity of Wisconsin School of Medicine, Department of Physiology, Madison, WI 53706
Noriaki Ikemoto
bBoston Biomedical Research Institute, Department of Muscle Research, Watertown, MA 02472
Martin F. Schneider
aUniversity of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Baltimore, MD 21201
Abbreviations used in this paper: CICR, Ca2+-induced Ca2+-release; DHPR, dihydropyridine receptors; FDHM, full duration at half maximum amplitude; FWHM, full width at half maximum amplitude; MH, malignant hyperthermia.
Received:
May 14 2001
Revision Requested:
November 09 2001
Accepted:
November 14 2001
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 2002 The Rockefeller University Press
2002
The Rockefeller University Press
J Gen Physiol (2002) 119 (1): 15–32.
Article history
Received:
May 14 2001
Revision Requested:
November 09 2001
Accepted:
November 14 2001
Citation
Alexander Shtifman, Christopher W. Ward, Takeshi Yamamoto, Jianli Wang, Beth Olbinski, Hector H. Valdivia, Noriaki Ikemoto, Martin F. Schneider; Interdomain Interactions within Ryanodine Receptors Regulate Ca2+ Spark Frequency in Skeletal Muscle . J Gen Physiol 1 January 2002; 119 (1): 15–32. doi: https://doi.org/10.1085/jgp.119.1.15
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