Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, United States.
Elife. 2019 Nov 14;8:e51212. doi: 10.7554/eLife.51212.
Activation of TRPV1 channels in sensory neurons results in opening of a cation permeation pathway that triggers the sensation of pain. Opening of TRPV1 has been proposed to involve two gates that appear to prevent ion permeation in the absence of activators: the ion selectivity filter on the external side of the pore and the S6 helices that line the cytosolic half of the pore. Here we measured the access of thiol-reactive ions across the selectivity filters in rodent TRPV1-3 channels. Although our results are consistent with structural evidence that the selectivity filters in these channels are dynamic, they demonstrate that cations can permeate the ion selectivity filters even when channels are closed. Our results suggest that the selectivity filters in TRPV1-3 channels do not function as activation gates but might contribute to coupling structural rearrangements in the external pore to those in the cytosolic S6 gate.
激活感觉神经元上的 TRPV1 通道会导致阳离子渗透途径的打开,从而引发疼痛感觉。TRPV1 的打开被认为涉及两个门控,在没有激活剂的情况下似乎可以防止离子渗透:位于孔外部的离子选择性过滤器和构成孔胞质一半的 S6 螺旋。在这里,我们测量了巯基反应离子穿过啮齿动物 TRPV1-3 通道的选择性过滤器的进入情况。尽管我们的结果与结构证据一致,即这些通道中的选择性过滤器是动态的,但它们表明,即使通道关闭,阳离子也可以渗透离子选择性过滤器。我们的结果表明,TRPV1-3 通道中的选择性过滤器不作为激活门控发挥作用,但可能有助于将外部孔中的结构重排与胞质 S6 门中的结构重排联系起来。