%0 Journal Article %1 Rios_1993_449 %A R�os, E. %A Karhanek, M. %A Ma, J. %A Gonz�lez, A. %D 1993 %J J. Gen. Physiol. %K Acid; Allosteric Animals; Anura; Biological; Calcium Calcium; Channel Channels; Compounds; Contraction; Electric Feedback; Gating; Ion Kinetics; Models, Muscle Muscles; Perchloric Regulation; Sodium Stimulation; Synaptic Transmission %N 3 %P 449--481 %T An allosteric model of the molecular interactions of excitation-contraction coupling in skeletal muscle. %V 102 %X A contact interaction is proposed to exist between the voltage sensor of the transverse tubular membrane of skeletal muscle and the calcium release channel of the sarcoplasmic reticulum. This interaction is given a quantitative formulation inspired in the Monod, Wyman, and Changeux model of allosteric transitions in hemoglobin (Monod, J., J. Wyman, and J.-P. Changeux. 1965. Journal of Molecular Biology. 12:88-118), and analogous to one proposed by Marks and Jones for voltage-dependent Ca channels (Marks, T. N., and S. W. Jones. 1992. Journal of General Physiology. 99:367-390). The allosteric protein is the calcium release channel, a homotetramer, with two accessible states, closed and open. The kinetics and equilibrium of this transition are modulated by voltage sensors (dihydropyridine receptors) pictured as four units per release channel, each undergoing independent voltage-driven transitions between two states (resting and activating). For each voltage sensor that moves to the activating state, the tendency of the channel to open increases by an equal (large) factor. The equilibrium and kinetic equations of the model are solved and shown to reproduce well a number of experimentally measured relationships including: charge movement (Q) vs. voltage, open probability of the release channel (Po) vs. voltage, the transfer function relationship Po vs. Q, and the kinetics of charge movement, release activation, and deactivation. The main consequence of the assumption of allosteric coupling is that primary effects on the release channel are transmitted backward to the voltage sensor and give secondary effects. Thus, the model reproduces well the effects of perchlorate, described in the two previous articles, under the assumption that the primary effect is to increase the intrinsic tendency of the release channel to open, with no direct effects on the voltage sensor. This modification of the open-closed equilibrium of the release channel causes a shift in the equilibrium dependency of charge movement with voltage. The paradoxical slowing of charge movement by perchlorate also results from reciprocal effects of the channel on the allosterically coupled voltage sensors. The observations of the previous articles plus the simulations in this article constitute functional evidence of allosteric transmission.

@article{Rios_1993_449, abstract = {A contact interaction is proposed to exist between the voltage sensor of the transverse tubular membrane of skeletal muscle and the calcium release channel of the sarcoplasmic reticulum. This interaction is given a quantitative formulation inspired in the Monod, Wyman, and Changeux model of allosteric transitions in hemoglobin (Monod, J., J. Wyman, and J.-P. Changeux. 1965. Journal of Molecular Biology. 12:88-118), and analogous to one proposed by Marks and Jones for voltage-dependent Ca channels (Marks, T. N., and S. W. Jones. 1992. Journal of General Physiology. 99:367-390). The allosteric protein is the calcium release channel, a homotetramer, with two accessible states, closed and open. The kinetics and equilibrium of this transition are modulated by voltage sensors (dihydropyridine receptors) pictured as four units per release channel, each undergoing independent voltage-driven transitions between two states (resting and activating). For each voltage sensor that moves to the activating state, the tendency of the channel to open increases by an equal (large) factor. The equilibrium and kinetic equations of the model are solved and shown to reproduce well a number of experimentally measured relationships including: charge movement (Q) vs. voltage, open probability of the release channel (Po) vs. voltage, the transfer function relationship Po vs. Q, and the kinetics of charge movement, release activation, and deactivation. The main consequence of the assumption of allosteric coupling is that primary effects on the release channel are transmitted backward to the voltage sensor and give secondary effects. Thus, the model reproduces well the effects of perchlorate, described in the two previous articles, under the assumption that the primary effect is to increase the intrinsic tendency of the release channel to open, with no direct effects on the voltage sensor. This modification of the open-closed equilibrium of the release channel causes a shift in the equilibrium dependency of charge movement with voltage. The paradoxical slowing of charge movement by perchlorate also results from reciprocal effects of the channel on the allosterically coupled voltage sensors. The observations of the previous articles plus the simulations in this article constitute functional evidence of allosteric transmission.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {R�os, E. and Karhanek, M. and Ma, J. and Gonz�lez, A.}, biburl = {https://www.bibsonomy.org/bibtex/20fd905f5f1ad5ffef1e1c83c403d04da/hake}, description = {The whole bibliography file I use.}, file = {Rios_1993_449.pdf:Rios_1993_449.pdf:PDF;Rios_1993_449.pdf:Rios_1993_449.pdf:PDF}, institution = {Department of Physiology, Rush University School of Medicine, Chicago, Illinois 60612.}, interhash = {dc8ba4bc48914c0bceb5b082b9adf77f}, intrahash = {0fd905f5f1ad5ffef1e1c83c403d04da}, journal = {J. Gen. Physiol.}, keywords = {Acid; Allosteric Animals; Anura; Biological; Calcium Calcium; Channel Channels; Compounds; Contraction; Electric Feedback; Gating; Ion Kinetics; Models, Muscle Muscles; Perchloric Regulation; Sodium Stimulation; Synaptic Transmission}, month = Sep, number = 3, pages = {449--481}, pmid = {8245819}, timestamp = {2009-06-03T11:21:28.000+0200}, title = {An allosteric model of the molecular interactions of excitation-contraction coupling in skeletal muscle.}, volume = 102, year = 1993 }