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Being flexible: the voltage-controllable activation gate of Kv channels

Journal

FRONTIERS IN PHARMACOLOGY
Volume 3, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2012.00168

Keywords

bundle crossing gate; glycine and PXP hinge point; pore opening and closure; selectivity fitter; shaker potassium channel; voltage-dependent gating

Funding

  1. Research Foundation Flanders (FWO, Fonds voor Wetenschappelijk Onderzoek Vlaanderen) [G.0449.11, 1.5.087.11N]

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Kv channels form voltage-dependent potassium selective pores in the outer cell membrane and are composed out of four alpha-subunits, each having six membrane-spanning alpha-helices (S1-S6). The alpha-subunits tetramerize such that the S5-S6 pore domains co-assemble into a centrally located K+ pore which is surrounded by four operational voltage-sensing domains (VSD) that are each formed by the S1-S4 segments. Consequently, each subunit is capable of responding to changes in membrane potential and dictates whether the pore should be conductive or not. K+ permeation through the pore can be sealed off by two separate gates in series: (a) at the inner S6 bundle crossing (BC gate) and (b) at the level of the selectivity filter (SF gate) located at the extracellular entrance of the pore. Within the last years a general consensus emerged that a direct communication between the S4S5-linker and the bottom part of S6 (S6(c)) constitutes the coupling with the VSD thus making the BC gate the main voltage-controllable activation gate. While the BC gate listens to the VSD, the SF changes its conformation depending on the status of the BC gate. Through the eyes of an entering K+ ion, the operation of the BC gate apparatus can be compared with the iris-like motion of the diaphragm from a camera whereby its diameter widens. Two main gating motions have been proposed to create this BC gate widening: (1) tilting of the helix whereby the S6 converts from a straight a-helix to a tilted one or (2) swiveling of the S60 whereby the S6 remains bent. Such motions require a flexible hinge that decouples the pre-and post-hinge segment. Roughly at the middle of the S6 there exists a highly conserved glycine residue and a tandem proline motif that seem to fulfill the role of a gating hinge which allows for tilting/swiveling/rotations of the post-hinge S6 segment. In this review we delineate our current view on the operation of the BC gate for controlling K+ permeation in Kv channels.

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