quantitative modeling of currents from a voltage gated ion channel undergoing fast inactivation定量建模的电流电压门控离子通道进行快速失活.pdfVIP

quantitative modeling of currents from a voltage gated ion channel undergoing fast inactivation定量建模的电流电压门控离子通道进行快速失活.pdf

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quantitative modeling of currents from a voltage gated ion channel undergoing fast inactivation定量建模的电流电压门控离子通道进行快速失活

Quantitative Modeling of Currents from a Voltage Gated Ion Channel Undergoing Fast Inactivation Carlos J. Camacho* Department of Computational Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America Abstract Ion channels play a central role in setting gradients of ion concentration and electrostatic potentials, which in turn regulate sensory systems and other functions. Based on the structure of the open configuration of the Kv1.2 channel and the suggestion that the two ends of the N-terminal inactivating peptide form a bivalent complex that simultaneously blocks the channel pore and binds to the cytoplasmic T1 domain, we propose a six state kinetic model that for the first time reproduces the kinetics of recovery of the Drosophila Shaker over the full range of time scales and hyperpolarization potentials, including tail currents. The model is motivated by a normal mode analysis of the inactivated channel that suggests that a displacement consistent with models of the closed state propagates to the T1 domain via the S1-T1 linker. This motion stretches the bound (inactivating) peptide, hastening the unblocking of the pore. This pulling force is incorporated into the rates of the open to blocked states, capturing the fast recovery phase of the current for repolarization events shorter than 1 ms. If the membrane potential is hyperpolarized, essential dynamics further suggests that the T1 domain returns to a configuration where the peptide is unstretched and the S1-T1 linker is extended. Coupling this novel hyperpolarized substate to the closed, open and blocked pore states is enough to quantitatively estimate the n

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