%0 Journal Article %1 Zahr_1999_787 %A Zahradn�kov�, A. %A Zahradn�k, I. %A Gy�rke, I. %A Gy�rke, S. %D 1999 %J J. Gen. Physiol. %K 10578015 Acetic Acids, Agents, Algorithms, Animals, Bilayers, Biological, Calcium Calcium, Cardiac, Cells, Channel Channel, Chelating Cultured, Dogs, Dose-Response Drug, Ethylenediamines, Gating, Gov't, Heart, In Ion Kinetics, Lipid Magnesium, Microsomes, Models, Myocardium, Myocytes, Non-U.S. P.H.S., Patch-Clamp Photolysis, Receptor Relationship, Release Research Reticulum, Ryanodine Sarcoplasmic Signaling, Support, Techniques, U.S. Vitro, %N 6 %P 787--798 %T Rapid activation of the cardiac ryanodine receptor by submillisecond calcium stimuli. %U http://www.jgp.org/cgi/content/full/114/6/787 %V 114 %X The local control concept of excitation-contraction coupling in the heart postulates that the activity of the sarcoplasmic reticulum ryanodine receptor channels (RyR) is controlled by Ca$^2+$ entry through adjoining sarcolemmal single dihydropyridine receptor channels (DHPRs). One unverified premise of this hypothesis is that the RyR must be fast enough to track the brief (<0.5 ms) Ca$^2+$ elevations accompanying single DHPR channel openings. To define the kinetic limits of effective trigger Ca$^2+$ signals, we recorded activity of single cardiac RyRs in lipid bilayers during rapid and transient increases in Ca$^2+$ generated by flash photolysis of DM-nitrophen. Application of such Ca$^2+$ spikes (amplitude approximately 10-30 microM, duration approximately 0.1-0.4 ms) resulted in activation of the RyRs with a probability that increased steeply (apparent Hill slope approximately 2.5) with spike amplitude. The time constants of RyR activation were 0.07-0.27 ms, decreasing with spike amplitude. To fit the rising portion of the open probability, a single exponential function had to be raised to a power n approximately 3. We show that these data could be adequately described with a gating scheme incorporating four sequential Ca$^2+$-sensitive closed states between the resting and the first open states. These results provide evidence that brief Ca$^2+$ triggers are adequate to activate the RyR, and support the possibility that RyR channels are governed by single DHPR openings. They also provide evidence for the assumption that RyR activation requires binding of multiple Ca$^2+$ ions in accordance with the tetrameric organization of the channel protein.

@article{Zahr_1999_787, abstract = {The local control concept of excitation-contraction coupling in the heart postulates that the activity of the sarcoplasmic reticulum ryanodine receptor channels (RyR) is controlled by {C}a$^{2+}$ entry through adjoining sarcolemmal single dihydropyridine receptor channels (DHPRs). One unverified premise of this hypothesis is that the RyR must be fast enough to track the brief (<0.5 ms) {C}a$^{2+}$ elevations accompanying single DHPR channel openings. To define the kinetic limits of effective trigger {C}a$^{2+}$ signals, we recorded activity of single cardiac RyRs in lipid bilayers during rapid and transient increases in {C}a$^{2+}$ generated by flash photolysis of DM-nitrophen. Application of such {C}a$^{2+}$ spikes (amplitude approximately 10-30 microM, duration approximately 0.1-0.4 ms) resulted in activation of the RyRs with a probability that increased steeply (apparent Hill slope approximately 2.5) with spike amplitude. The time constants of RyR activation were 0.07-0.27 ms, decreasing with spike amplitude. To fit the rising portion of the open probability, a single exponential function had to be raised to a power n approximately 3. We show that these data could be adequately described with a gating scheme incorporating four sequential {C}a$^{2+}$-sensitive closed states between the resting and the first open states. These results provide evidence that brief {C}a$^{2+}$ triggers are adequate to activate the RyR, and support the possibility that RyR channels are governed by single DHPR openings. They also provide evidence for the assumption that RyR activation requires binding of multiple {C}a$^{2+}$ ions in accordance with the tetrameric organization of the channel protein.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {Zahradn�kov�, A. and Zahradn�k, I. and Gy�rke, I. and Gy�rke, S.}, biburl = {https://www.bibsonomy.org/bibtex/2083b767445fca91eef813d8063b4fe6b/hake}, description = {The whole bibliography file I use.}, file = {Zahr_1999_787.pdf:Zahr_1999_787.pdf:PDF}, interhash = {199300d783506b45309aca59e6550553}, intrahash = {083b767445fca91eef813d8063b4fe6b}, journal = {J. Gen. Physiol.}, keywords = {10578015 Acetic Acids, Agents, Algorithms, Animals, Bilayers, Biological, Calcium Calcium, Cardiac, Cells, Channel Channel, Chelating Cultured, Dogs, Dose-Response Drug, Ethylenediamines, Gating, Gov't, Heart, In Ion Kinetics, Lipid Magnesium, Microsomes, Models, Myocardium, Myocytes, Non-U.S. P.H.S., Patch-Clamp Photolysis, Receptor Relationship, Release Research Reticulum, Ryanodine Sarcoplasmic Signaling, Support, Techniques, U.S. Vitro,}, month = Dec, number = 6, pages = {787--798}, pdf = {Zahr_1999_787.pdf}, pmid = {10578015}, timestamp = {2009-06-03T11:21:38.000+0200}, title = {Rapid activation of the cardiac ryanodine receptor by submillisecond calcium stimuli.}, url = {http://www.jgp.org/cgi/content/full/114/6/787}, volume = 114, year = 1999 }