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恶性疟原虫线粒体DNA聚合酶的部分纯化及特性分析

Partial purification and characterization of mitochondrial DNA polymerase from Plasmodium falciparum.

作者信息

Chavalitshewinkoon-Petmitr P, Chawprom S, Naesens L, Balzarini J, Wilairat P

机构信息

Department of Protozoology, Faculty of Tropical Medicine, Mahidol University, 420/6 Rajvithi Road, Bangkok 10400, Thailand.

出版信息

Parasitol Int. 2000 Dec;49(4):279-88. doi: 10.1016/s1383-5769(00)00057-x.

Abstract

Mitochondria of chloroquine-resistant Plasmodium falciparum (K1 strain) were isolated from mature trophozoites by differential centrifugation. The mitochondrial marker enzyme cytochrome c reductase was employed to monitor the steps of mitochondria isolation. Partial purification of DNA polymerase from P. falciparum mitochondria was performed using fast protein liquid chromatography (FPLC). DNA polymerase of P. falciparum mitochondria was characterized as a gamma-like DNA polymerase based on its sensitivity to the inhibitors aphidicolin, N-ethylmaleimide and 9-beta-D-arabinofuranosyladenine-5'-triphosphate. In contrast, the enzyme was found to be strongly resistant to 2',3'-dideoxythymidine-5'-triphosphate (IC(50)>400 microM) and differed in this aspect from the human homologue, possibly indicating structural differences between human and P. falciparum DNA polymerase gamma. In addition, the DNA polymerase of parasite mitochondria was shown to be resistant (IC(50)>1 mM) to the nucleotide analogue (S)-1-[3-hydroxy-2-phosphonylmethoxypropyl]adenine diphosphate (HPMPApp).

摘要

通过差速离心从成熟滋养体中分离出氯喹抗性恶性疟原虫(K1株)的线粒体。使用线粒体标记酶细胞色素c还原酶来监测线粒体分离步骤。利用快速蛋白质液相色谱(FPLC)对恶性疟原虫线粒体的DNA聚合酶进行部分纯化。基于恶性疟原虫线粒体DNA聚合酶对抑制剂阿非迪霉素、N - 乙基马来酰胺和9 - β - D - 阿拉伯呋喃糖基腺嘌呤 - 5'-三磷酸的敏感性,将其鉴定为γ样DNA聚合酶。相比之下,该酶对2',3'-双脱氧胸苷 - 5'-三磷酸具有很强的抗性(IC(50)>400 microM),在这方面与人类同源物不同,这可能表明人类和恶性疟原虫DNA聚合酶γ之间存在结构差异。此外,寄生虫线粒体的DNA聚合酶对核苷酸类似物(S)-1 - [3 - 羟基 - 2 - 膦酰甲氧基丙基]腺嘌呤二磷酸(HPMPApp)具有抗性(IC(50)>1 mM)。

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