Distinct contributions of different structural regions to the current kinetics of the Cav3.3 T-type Ca<SUP>2+</SUP> channel

초록

Electrophysiological characterization of T-type Ca2+ channel isoforms (Ca(v)3.1, Ca(v)3.2, and Ca(v)3.3) has shown that all of the isoforms are low voltage-activated around resting membrane potential, but their current kinetics are distinctly different, with the activation and inactivation kinetics of the Ca(v)3.1 and Ca(v)3.2 channels being much faster than those of the Ca(v)3.3 channel. We previously reported that multiple structural regions of the Ca(v)3.3 T-type channel participate in determining its current kinetics. Here we have evaluated the relative contributions of individual cytoplasmic and trans-membrane regions to the current kinetics of the channel, by systematically replacing individual regions of Ca(v)3.3 with the corresponding regions of Ca(v)3.1. Introduction of the Ca(v)3.1 III-IV loop into the Ca(v)3.3 backbone accelerated both the activation and inactivation kinetics more prominently than any other intracellular loop or tail. Among the trans-membrane domains, introduction of the domain 1 of Ca(v)3.1 into Ca(v)3.3 accelerated both the activation and inactivation kinetics most effectively. These findings suggest that the current kinetics of the Ca(v)33 channel are differentially controlled by several structural regions, among which the III-IV loop and domain I are the most prominent in governing both activation and inactivation kinetics. (C) 2008 Elsevier B.V. All rights reserved.

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