Recent Advances in Computer-Aided Structure-Based Drug Design on Ion Channels

被引:4
|
作者
Pliushcheuskaya, Palina [1 ]
Kuenze, Georg [1 ,2 ]
机构
[1] Univ Leipzig, Inst Drug Discovery, Med Fac, Bruderstr 34, D-04103 Leipzig, Germany
[2] Univ Leipzig, Interdisciplinary Ctr Bioinformat, Hartelstr 16-18, D-04107 Leipzig, Germany
关键词
ion channels; ion channel structure; drug design; virtual screening; ligand docking; molecular dynamics; CRYO-EM STRUCTURE; POTASSIUM CHANNELS; SODIUM-CHANNELS; CHEMBL DATABASE; RECEPTOR; DISCOVERY; MECHANISMS; PREDICTION; BINDING; MODELS;
D O I
10.3390/ijms24119226
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ion channels play important roles in fundamental biological processes, such as electric signaling in cells, muscle contraction, hormone secretion, and regulation of the immune response. Targeting ion channels with drugs represents a treatment option for neurological and cardiovascular diseases, muscular degradation disorders, and pathologies related to disturbed pain sensation. While there are more than 300 different ion channels in the human organism, drugs have been developed only for some of them and currently available drugs lack selectivity. Computational approaches are an indispensable tool for drug discovery and can speed up, especially, the early development stages of lead identification and optimization. The number of molecular structures of ion channels has considerably increased over the last ten years, providing new opportunities for structure-based drug development. This review summarizes important knowledge about ion channel classification, structure, mechanisms, and pathology with the main focus on recent developments in the field of computer-aided, structure-based drug design on ion channels. We highlight studies that link structural data with modeling and chemoinformatic approaches for the identification and characterization of new molecules targeting ion channels. These approaches hold great potential to advance research on ion channel drugs in the future.
引用
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页数:22
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