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从 物种中发现新型 Conotoxin 的方法。

Discovery Methodology of Novel Conotoxins from Species.

机构信息

Key Laboratory of Tropical Biological Resources, Ministry of Education, Hainan University, Haikou 570228, China.

Key Laboratory for Marine Drugs of Haikou, Hainan University, Haikou 570228, China.

出版信息

Mar Drugs. 2018 Oct 30;16(11):417. doi: 10.3390/md16110417.

Abstract

Cone snail venoms provide an ideal resource for neuropharmacological tools and drug candidates discovery, which have become a research hotspot in neuroscience and new drug development. More than 1,000,000 natural peptides are produced by cone snails, but less than 0.1% of the estimated conotoxins has been characterized to date. Hence, the discovery of novel conotoxins from the huge conotoxin resources with high-throughput and sensitive methods becomes a crucial key for the conotoxin-based drug development. In this review, we introduce the discovery methodology of new conotoxins from various species. It focuses on obtaining full N- to C-terminal sequences, regardless of disulfide bond connectivity through crude venom purification, conotoxin precusor gene cloning, venom duct transcriptomics, venom proteomics and multi-omic methods. The protocols, advantages, disadvantages, and developments of different approaches during the last decade are summarized and the promising prospects are discussed as well.

摘要

芋螺毒素为神经药理学工具和药物候选物的发现提供了理想的资源,这已成为神经科学和新药开发的研究热点。芋螺产生超过 100 万个天然肽,但迄今为止,只有不到 0.1%的估计芋螺毒素得到了表征。因此,用高通量和敏感的方法从巨大的芋螺毒素资源中发现新型芋螺毒素是基于芋螺毒素的药物开发的关键。在本文综述中,我们介绍了从各种物种中发现新型芋螺毒素的方法。重点是通过粗毒液纯化、前体基因克隆、毒液管转录组学、毒液蛋白质组学和多组学方法获得全长 N 端至 C 端序列,而不考虑二硫键连接。总结了过去十年中不同方法的方案、优缺点和发展,并讨论了有希望的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9743/6266589/20a854dce18e/marinedrugs-16-00417-g001.jpg

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