Channelpedia

PubMed 24270805


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Kir2.3



Title: Structural basis for Ca2+ selectivity of a voltage-gated calcium channel.

Authors: Lin Tang, Tamer M Gamal El-Din, Jian Payandeh, Gilbert Q Martinez, Teresa M Heard, Todd Scheuer, Ning Zheng, William A Catterall

Journal, date & volume: Nature, 2014 Jan 2 , 505, 56-61

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24270805


Abstract
Voltage-gated calcium (CaV) channels catalyse rapid, highly selective influx of Ca(2+) into cells despite a 70-fold higher extracellular concentration of Na(+). How CaV channels solve this fundamental biophysical problem remains unclear. Here we report physiological and crystallographic analyses of a calcium selectivity filter constructed in the homotetrameric bacterial NaV channel NaVAb. Our results reveal interactions of hydrated Ca(2+) with two high-affinity Ca(2+)-binding sites followed by a third lower-affinity site that would coordinate Ca(2+) as it moves inward. At the selectivity filter entry, Site 1 is formed by four carboxyl side chains, which have a critical role in determining Ca(2+) selectivity. Four carboxyls plus four backbone carbonyls form Site 2, which is targeted by the blocking cations Cd(2+) and Mn(2+), with single occupancy. The lower-affinity Site 3 is formed by four backbone carbonyls alone, which mediate exit into the central cavity. This pore architecture suggests a conduction pathway involving transitions between two main states with one or two hydrated Ca(2+) ions bound in the selectivity filter and supports a 'knock-off' mechanism of ion permeation through a stepwise-binding process. The multi-ion selectivity filter of our CaVAb model establishes a structural framework for understanding the mechanisms of ion selectivity and conductance by vertebrate CaV channels.