Netirojjanakul Chawita, Miranda Les P
Therapeutic Discovery, Amgen Inc., One Amgen Center Drive, Thousand Oaks, CA 91320, USA.
Therapeutic Discovery, Amgen Inc., One Amgen Center Drive, Thousand Oaks, CA 91320, USA.
Curr Opin Chem Biol. 2017 Jun;38:70-79. doi: 10.1016/j.cbpa.2017.03.004. Epub 2017 Apr 1.
The number of new toxin peptide discoveries has been rapidly growing in the past few decades. Because of progress in proteomics, sequencing technologies, and high throughput bioassays, the search for new toxin peptides from venom collections and potency optimization has become manageable. However, to date, only six toxin peptide-derived therapeutics have been approved by the USFDA, with only one, ziconotide, for a pain indication. The challenge of venom-derived peptide therapeutic development remains in improving selectivity to the target and more importantly, in delivery of these peptides to the sites of action in the central and peripheral nervous system. In this review, we highlight peptide toxins that target major therapeutic targets for pain and discuss the challenges of developing toxin peptides as potential therapeutics.
在过去几十年中,新毒素肽的发现数量一直在迅速增长。由于蛋白质组学、测序技术和高通量生物测定技术的进步,从毒液库中寻找新毒素肽以及优化其效力已变得可行。然而,迄今为止,美国食品药品监督管理局(USFDA)仅批准了六种源自毒素肽的疗法,其中只有一种,即齐考诺肽,用于止痛适应症。源自毒液的肽类治疗药物开发面临的挑战仍然在于提高对靶点的选择性,更重要的是,在于将这些肽递送至中枢和外周神经系统的作用部位。在这篇综述中,我们重点介绍了针对主要疼痛治疗靶点的肽毒素,并讨论了开发毒素肽作为潜在治疗药物所面临的挑战。