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原虫病原体中的多胺。

Polyamines in protozoan pathogens.

机构信息

From the Departments of Biochemistry and Pharmacology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9038

出版信息

J Biol Chem. 2018 Nov 30;293(48):18746-18756. doi: 10.1074/jbc.TM118.003342. Epub 2018 Oct 17.

Abstract

Polyamines are polycationic organic amines that are required for all eukaryotic life, exemplified by the polyamine spermidine, which plays an essential role in translation. They also play more specialized roles that differ across species, and their chemical versatility has been fully exploited during the evolution of protozoan pathogens. These eukaryotic pathogens, which cause some of the most globally widespread infectious diseases, have acquired species-specific polyamine-derived metabolites with essential cellular functions and have evolved unique mechanisms that regulate their core polyamine biosynthetic pathways. Many of these parasitic species have lost enzymes and or transporters from the polyamine metabolic pathway that are found in the human host. These pathway differences have prompted drug discovery efforts to target the parasite polyamine pathways, and indeed, the only clinically approved drug targeting the polyamine biosynthetic pathway is used to manage human African trypanosomiasis. This Minireview will primarily focus on polyamine metabolism and function in , , and species, which are the causative agents of human African trypanosomiasis (HAT) and Chagas disease, Leishmaniasis, and malaria, respectively. Aspects of polyamine metabolism across a diverse group of protozoan pathogens will also be explored.

摘要

多胺是带正电荷的有机胺,是所有真核生物生命所必需的,以多胺精脒为例,它在翻译中起着至关重要的作用。它们还具有在不同物种中存在差异的更专业化作用,其化学多功能性在原生动物病原体的进化过程中得到了充分利用。这些真核病原体引起了一些在全球范围内广泛传播的传染病,它们获得了具有重要细胞功能的特定物种来源的多胺衍生代谢物,并进化出了独特的机制来调节其核心多胺生物合成途径。许多这些寄生物种已经失去了在人类宿主中发现的多胺代谢途径中的酶和/或转运蛋白。这些途径的差异促使药物发现工作以寄生虫多胺途径为靶点,事实上,唯一临床批准的靶向多胺生物合成途径的药物用于治疗人类非洲锥虫病。这篇综述将主要集中在多胺代谢和功能方面,在 , 和 物种,它们分别是引起人类非洲锥虫病(HAT)和恰加斯病、利什曼病和疟疾的病原体。还将探讨一组多样化的原生动物病原体中的多胺代谢的各个方面。

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