Conotoxins Targeting Nicotinic Acetylcholine Receptors: An Overview

Marine Drugs

Eline K. M. Lebbe¹  Steve Peigneur¹  Isuru Wijesekara¹ 

[1] Toxicology and Pharmacology, KU Leuven (University of Leuven), O&N2 P.O.Box 922, Herestraat 49, 3000 Leuven, Belgium;

关键词: nicotinic acetylcholine receptor;    cone snail toxins;    α-conotoxins;    mode of action;    working mechanism;    acetylcholine binding protein;    crystallography;    docking model;   

DOI  :  10.3390/md12052970

来源: mdpi

【 摘 要 】

Marine snails of the genus Conus are a large family of predatory gastropods with an unparalleled molecular diversity of pharmacologically active compounds in their venom. Cone snail venom comprises of a rich and diverse cocktail of peptide toxins which act on a wide variety of ion channels such as voltage-gated sodium- (Na_V), potassium- (K_V), and calcium- (Ca_V) channels as well as nicotinic acetylcholine receptors (nAChRs) which are classified as ligand-gated ion channels. The mode of action of several conotoxins has been the subject of investigation, while for many others this remains unknown. This review aims to give an overview of the knowledge we have today on the molecular pharmacology of conotoxins specifically interacting with nAChRs along with the structure–function relationship data.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.