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Molecular Characterization of an rsmD-Like rRNA Methyltransferase from the Wolbachia Endosymbiont of Brugia malayi and Antifilarial Activity of Specific Inhibitors of the Enzyme

机译:马来亚布鲁氏菌的Wolbachia内生菌的rsmD样rRNA甲基转移酶的分子表征和酶的特定抑制剂的抗丝活性

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摘要

The endosymbiotic organism Wolbachia is an attractive antifilarial drug target. Here we report on the cloning and expression of an rsmD-like rRNA methyltransferase from the Wolbachia endosymbiont of Brugia malayi, its molecular properties, and assays for specific inhibitors. The gene was found to be expressed in all the major life stages of B. malayi. The purified enzyme expressed in Escherichia coli was found to be in monomer form in its native state. The activities of the specific inhibitors (heteroaryl compounds) against the enzyme were tested with B. malayi adult and microfilariae for 7 days in vitro at various concentrations, and NSC-659390 proved to be the most potent compound (50% inhibitory concentration [IC50], 0.32 μM), followed by NSC-658343 (IC50, 4.13 μM) and NSC-657589 (IC50, 7.5 μM). On intraperitoneal administration at 5 mg/kg of body weight for 7 days to adult jirds into which B. malayi had been transplanted intraperitoneally, all the compounds killed a significant proportion of the implanted worms. A very similar result was observed in infected mastomys when inhibitors were administered. Docking studies of enzyme and inhibitors and an in vitro tryptophan quenching experiment were also performed to understand the binding mode and affinity. The specific inhibitors of the enzyme showed a higher affinity for the catalytic site of the enzyme than the nonspecific inhibitors and were found to be potent enough to kill the worm (both adults and microfilariae) in vitro as well as in vivo in a matter of days at micromolar concentrations. The findings suggest that these compounds be evaluated against other pathogens possessing a methyltransferase with a DPPY motif and warrant the design and synthesis of more such inhibitors.
机译:内共生生物Wolbachia是有吸引力的抗丝虫药物靶标。在这里,我们报道了来自马来西亚布鲁氏菌的Wolbachia内共生体的rsmD样rRNA甲基转移酶的克隆和表达,其分子特性以及特异性抑制剂的测定。发现该基因在马来芽孢杆菌的所有主要生命阶段都有表达。发现在大肠杆菌中表达的纯化酶为天然形式的单体形式。在不同浓度下,用马来芽孢杆菌(B. malayi)成虫和微丝虫对特定抑制剂(杂芳基化合物)的活性进行了体外7天的测试,证明NSC-659390是最有效的化合物(抑制浓度为50%[IC50] (0.32μM),然后是NSC-658343(IC50,4.13μM)和NSC-657589(IC50,7.5μM)。在腹腔内以5 mg / kg体重腹膜内施用了7天的成虫后,所有化合物都杀死了很大一部分植入的蠕虫。当施用抑制剂时,在感染的乳腺切开术中观察到非常相似的结果。还进行了酶和抑制剂的对接研究以及体外色氨酸猝灭实验,以了解结合模式和亲和力。该酶的特异性抑制剂对酶催化位点的亲和力高于非特异性抑制剂,并且被发现足以在几天内和体外杀死蠕虫(成虫和微丝虫)。在微摩尔浓度。研究结果表明,可以针对具有DPPY基序的甲基转移酶的其他病原体对这些化合物进行评估,并可以设计和合成更多此类抑制剂。

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