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用于肉毒杆菌神经毒素的金属蛋白酶抑制剂类候选药物的最新进展。

Recent developments with metalloprotease inhibitor class of drug candidates for botulinum neurotoxins.

作者信息

Kumar Gyanendra, Swaminathan Subramanyam

机构信息

Biological, Environmental & Climate Sciences Department, 50 Bell Avenue, Building 463, Brookhaven National Laboratory, Upton, NY 11973, USA.

出版信息

Curr Top Med Chem. 2015;15(7):685-95. doi: 10.2174/1568026615666150309150338.

Abstract

Botulinum Neurotoxins are the most poisonous of all toxins with lethal dose in nanogram quantities. They are potential biological warfare and bioterrorism agents due to their high toxicity and ease of preparation. On the other hand BoNTs are also being increasingly used for therapeutic and cosmetic purposes, and with that the chances of accidental overdose are increasing. And despite the potential damage they could cause to human health, there are no post-intoxication drugs available so far. But progress is being made in this direction. The crystal structures in native form and bound with substrate peptides have been determined, and these are enabling structure-based drug discovery possible. High throughput assays have also been designed to speed up the screening progress. Substrate-based and small molecule inhibitors have been identified. But turning high affinity inhibitors into clinically viable drug candidates has remained a challenge. We discuss here the latest developments and the future challenges in drug discovery for Botulinum neurotoxins.

摘要

肉毒杆菌神经毒素是所有毒素中最具毒性的,致死剂量仅为纳克级。由于其高毒性和易于制备的特点,它们是潜在的生物战和生物恐怖主义制剂。另一方面,肉毒杆菌神经毒素也越来越多地用于治疗和美容目的,因此意外过量使用的可能性也在增加。尽管它们可能对人类健康造成潜在损害,但目前尚无中毒后可用的药物。不过在这方面正在取得进展。已确定了天然形式以及与底物肽结合的晶体结构,这使得基于结构的药物发现成为可能。还设计了高通量测定法以加快筛选进程。已鉴定出基于底物的和小分子抑制剂。但是将高亲和力抑制剂转化为临床上可行的候选药物仍然是一项挑战。我们在此讨论肉毒杆菌神经毒素药物发现的最新进展和未来挑战。

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