1. Academic Validation
  2. Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channels

Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channels

  • Proc Natl Acad Sci U S A. 2023 Oct 17;120(42):e2220029120. doi: 10.1073/pnas.2220029120.
Yun-Ting Chen # 1 Mee Ra Hong # 2 Xin-Jun Zhang # 3 James Kostas 2 Yuxing Li 3 Richard L Kraus 3 Vincent P Santarelli 3 Deping Wang 2 Yacob Gomez-Llorente 1 Alexei Brooun 2 Corey Strickland 1 Stephen M Soisson 2 Daniel J Klein 2 Anthony T Ginnetti 4 Michael J Marino 3 Shawn J Stachel 4 Andrii Ishchenko 2
Affiliations

Affiliations

  • 1 Computational and Structural Chemistry, Merck & Co., Inc., Kenilworth, NJ 07033.
  • 2 Computational and Structural Chemistry, Merck & Co., Inc., West Point, PA 19486.
  • 3 Department of Neuroscience, Merck & Co., Inc., West Point, PA 19486.
  • 4 Discovery Chemistry, Merck & Co., Inc., West Point, PA 19486.
  • # Contributed equally.
Abstract

Voltage-gated potassium channels (Kv) are tetrameric membrane proteins that provide a highly selective pathway for potassium ions (K+) to diffuse across a hydrophobic cell membrane. These unique voltage-gated cation channels detect changes in membrane potential and, upon activation, help to return the depolarized cell to a resting state during the repolarization stage of each action potential. The Kv3 family of potassium channels is characterized by a high activation potential and rapid kinetics, which play a crucial role for the fast-spiking neuronal phenotype. Mutations in the Kv3.1 channel have been shown to have implications in various neurological diseases like epilepsy and Alzheimer's disease. Moreover, disruptions in neuronal circuitry involving Kv3.1 have been correlated with negative symptoms of schizophrenia. Here, we report the discovery of a novel positive modulator of Kv3.1, investigate its biophysical properties, and determine the cryo-EM structure of the compound in complex with Kv3.1. Structural analysis reveals the molecular determinants of positive modulation in Kv3.1 channels by this class of compounds and provides additional opportunities for rational drug design for the treatment of associated neurological disorders.

Keywords

cryo-EM; positive modulator; structure; turret domain; voltage-gated ion channel.

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