Martínez-Hernández Luis, López-Vera Estuardo, Aguilar Manuel B
Posgrado en Ciencias Biológicas, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Laboratorio de Toxinología Marina, Unidad Académica de Ecología y Biodiversidad Acuática, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Toxins (Basel). 2024 Nov 22;16(12):504. doi: 10.3390/toxins16120504.
Toxins from snails are peptides characterized by a great structural and functional diversity. They have a high affinity for a wide range of membrane proteins such as ion channels, neurotransmitter transporters, and G protein-coupled receptors. Potassium ion channels are integral proteins of cell membranes that play vital roles in physiological processes in muscle and neuron cells, among others, and reports in the literature indicate that perturbation in their function (by mutations or ectopic expression) may result in the development and progression of different ailments in humans. This review aims to gather as much information as possible about toxins (conotoxins) with an effect on potassium channels and/or currents, with a perspective of exploring the possibility of finding or developing a possible drug candidate from these toxins. The research indicates that, among the more than 900 species described for this genus, in only 14 species of the >100 studied to date have such toxins been found (classified according to the most specific evidence for each case), as follows: 17 toxins with activity on two groups of potassium channels (Kv and KCa), 4 toxins with activity on potassium currents, and 5 toxins that are thought to inhibit potassium channels by symptomatology and/or a high sequence similarity.
蜗牛毒素是一类具有高度结构和功能多样性的肽。它们对多种膜蛋白具有高亲和力,如离子通道、神经递质转运体和G蛋白偶联受体。钾离子通道是细胞膜的整合蛋白,在肌肉和神经细胞等的生理过程中发挥着至关重要的作用,文献报道表明其功能的扰动(通过突变或异位表达)可能导致人类不同疾病的发生和发展。本综述旨在收集尽可能多的关于对钾通道和/或电流有影响的毒素(芋螺毒素)的信息,以期探索从这些毒素中寻找或开发潜在药物候选物的可能性。研究表明,在该属已描述的900多种物种中,迄今为止在已研究的100多种物种中,仅在14种物种中发现了此类毒素(根据每个案例的最具体证据分类),如下:17种对两组钾通道(Kv和KCa)有活性的毒素,4种对钾电流有活性的毒素,以及5种据推测通过症状学和/或高度序列相似性抑制钾通道的毒素。