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2000
Volume 16, Issue 16
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Ion channels are widely expressed in living cells and play critical roles in various cellular biological functions. Dysfunctional ion channels can cause a variety of diseases, making ion channels attractive targets for drug discovery. Computational approaches, such as molecular docking and molecular dynamic simulations, provide economic and efficient tools for finding modulators of ion channels and for elucidating the action mechanisms of small molecules. In this review, we focus primarily on four types of ion channels (voltage-gated, ligand-gated, acid-sensing, and virus matrix 2 ion channels). The current advancements in computer-aided drug discovery and design targeting ion channels are summarized. First, ligand-based studies for drug design are briefly outlined. Then, we focus on the structurebased studies targeting pore domains, endogenous binding sites and allosteric sites of ion channels. Moreover, we also review the contribution of computational methods to the field of ligand binding and unbinding pathways of ion channels. Finally, we propose future developments for the field.

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/content/journals/ctmc/10.2174/1568026616666160315142346
2016-07-01
2025-01-27
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  • Article Type:
    Research Article
Keyword(s): Allosteric site; Drug design; Drug discovery; Ion channel; Molecular dynamic simulation
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