4.3 Article

The activation gate controls steady-state inactivation and recovery from inactivation in Shaker

Journal

JOURNAL OF GENERAL PHYSIOLOGY
Volume 152, Issue 8, Pages -

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1085/jgp.202012591

Keywords

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Categories

Funding

  1. Hungarian Academy of Sciences [KTIA_NAP_13-2-2015-0009, KTIA_NAP_132-2017-0013]
  2. National Research Development and Innovation Office, Hungary [OTKA K132906, OTKA K119417]
  3. Ministry of Human Capacities, Hungary [EFOP-3.6.2-16-2017-00006]
  4. Ministry of Finance, Hungary [GINOP-2.3.2-15-2016-00015]
  5. European Union
  6. European Regional Development Fund
  7. New National Excellence Program of the Ministry for Innovation and Technology [UNKP-19-3-III-DE-92]
  8. National Institutes of Health [GM 52302]

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Despite major advances in the structure determination of ion channels, the sequence of molecular rearrangements at negative membrane potentials in voltage-gated potassium channels of the Shaker family remains unknown. Four major composite gating states are documented during the gating process: closed (C), open (O), open-inactivated (OI), and closed-inactivated (CI). Although many steps in the gating cycle have been clarified experimentally, the development of steady-state inactivation at negative membrane potentials and mandatory gating transitions for recovery from inactivation have not been elucidated. In this study, we exploit the biophysical properties of Shaker-IR mutants T449A/V474C and T449A/V476C to evaluate the status of the activation and inactivation gates during steady-state inactivation and upon locking the channel open with intracellular Cd2+. We conclude that at negative membrane potentials, the gating scheme of Shaker channels can be refined in two aspects. First, the most likely pathway for the development of steady-state inactivation is C -> O -> OI reversible arrow CI. Second, the OI -> CI transition is a prerequisite for recovery from inactivation. These findings are in accordance with the widely accepted view that tight coupling is present between the activation and C-type inactivation gates in Shaker and underscore the role of steady-state inactivation and recovery from inactivation as determinants of excitability.

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