A second S4 movement opens hyperpolarization-activated HCN channels.

Proc Natl Acad Sci U S A

Department of Physiology and Biophysics, University of Miami, Miami, FL 33136;

Published: September 2021

AI Article Synopsis

  • The rhythmic activity of pacemaker cells, like those in the sino-atrial node of the heart, relies on HCN channels, which are activated by hyperpolarization.
  • Research using voltage clamp fluorometry has shown that the S4 segment in HCN channels moves in two distinct steps when hyperpolarized, with the second step linked to channel opening.
  • A specific mutation (E356A) in sea urchin HCN channels alters this movement, allowing further insights on how S4 opening leads to the channel's activation and subsequent physiological responses.

Article Abstract

Rhythmic activity in pacemaker cells, as in the sino-atrial node in the heart, depends on the activation of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. As in depolarization-activated K channels, the fourth transmembrane segment S4 functions as the voltage sensor in hyperpolarization-activated HCN channels. But how the inward movement of S4 in HCN channels at hyperpolarized voltages couples to channel opening is not understood. Using voltage clamp fluorometry, we found here that S4 in HCN channels moves in two steps in response to hyperpolarizations and that the second S4 step correlates with gate opening. We found a mutation in sea urchin HCN channels that separate the two S4 steps in voltage dependence. The E356A mutation in S4 shifts the main S4 movement to positive voltages, but channel opening remains at negative voltages. In addition, E356A reveals a second S4 movement at negative voltages that correlates with gate opening. Cysteine accessibility and molecular models suggest that the second S4 movement opens up an intracellular crevice between S4 and S5 that would allow radial movement of the intracellular ends of S5 and S6 to open HCN channels.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449325PMC
http://dx.doi.org/10.1073/pnas.2102036118DOI Listing

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