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用于抗疟药物发现的生物合成平台。

A Biosynthetic Platform for Antimalarial Drug Discovery.

机构信息

Department of Chemistry, Imperial College London, London, United Kingdom.

Department of Infectious Diseases, Faculty of Medicine, Imperial College London, London, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.02129-19.

Abstract

Advances in synthetic biology have enabled the production of a variety of compounds using bacteria as a vehicle for complex compound biosynthesis. Violacein, a naturally occurring indole pigment with antibiotic properties, can be biosynthetically engineered in expressing its nonnative synthesis pathway. To explore whether this synthetic biosynthesis platform could be used for drug discovery, here we have screened bacterially derived violacein against the main causative agent of human malaria, We show the antiparasitic activity of bacterially derived violacein against the 3D7 laboratory reference strain as well as drug-sensitive and -resistant patient isolates, confirming the potential utility of this drug as an antimalarial agent. We then screen a biosynthetic series of violacein derivatives against growth. The varied activity of each derivative against asexual parasite growth points to the need to further develop violacein as an antimalarial. Towards defining its mode of action, we show that biosynthetic violacein affects the parasite actin cytoskeleton, resulting in an accumulation of actin signal that is independent of actin polymerization. This activity points to a target that modulates actin behavior in the cell either in terms of its regulation or its folding. More broadly, our data show that bacterial synthetic biosynthesis could become a suitable platform for antimalarial drug discovery, with potential applications in future high-throughput drug screening with otherwise chemically intractable natural products.

摘要

合成生物学的进步使我们能够利用细菌作为复杂化合物生物合成的载体来生产各种化合物。紫色素是一种天然存在的吲哚色素,具有抗生素特性,可以在表达其非天然合成途径的细菌中进行生物合成工程改造。为了探索这个合成生物合成平台是否可用于药物发现,我们在这里用细菌衍生的紫色素对人类疟疾的主要病原体 进行了筛选。我们证明了细菌衍生的紫色素对 3D7 实验室参考株以及对药物敏感和耐药的患者分离株的抗寄生虫活性,证实了这种药物作为抗疟药物的潜在用途。然后,我们对一系列生物合成的紫色素衍生物对 生长进行了筛选。每种衍生物对无性寄生虫生长的活性差异表明需要进一步开发紫色素作为抗疟药物。为了确定其作用模式,我们表明生物合成的紫色素会影响寄生虫肌动蛋白细胞骨架,导致肌动蛋白信号的积累,而肌动蛋白信号的积累与肌动蛋白聚合无关。这种活性表明存在一个靶标,它可以调节细胞中的肌动蛋白行为,无论是在其调节还是折叠方面。更广泛地说,我们的数据表明,细菌合成生物合成可以成为抗疟药物发现的合适平台,在未来具有挑战性的天然产物的高通量药物筛选中具有潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac7f/7179595/3ad9aab72edf/AAC.02129-19-f0001.jpg

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