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DprE2 是抗结核硝基咪唑化合物丙硫异烟胺和德拉马尼的分子靶标。

DprE2 is a molecular target of the anti-tubercular nitroimidazole compounds pretomanid and delamanid.

机构信息

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

Laboratory of Molecular and Microbial Biochemistry, School of Biological Sciences, University of Auckland, 3A Symonds Street, Auckland, 1010, New Zealand.

出版信息

Nat Commun. 2023 Jun 28;14(1):3828. doi: 10.1038/s41467-023-39300-z.

Abstract

Mycobacterium tuberculosis is one of the global leading causes of death due to a single infectious agent. Pretomanid and delamanid are new antitubercular agents that have progressed through the drug discovery pipeline. These compounds are bicyclic nitroimidazoles that act as pro-drugs, requiring activation by a mycobacterial enzyme; however, the precise mechanisms of action of the active metabolite(s) are unclear. Here, we identify a molecular target of activated pretomanid and delamanid: the DprE2 subunit of decaprenylphosphoribose-2'-epimerase, an enzyme required for the synthesis of cell wall arabinogalactan. We also provide evidence for an NAD-adduct as the active metabolite of pretomanid. Our results highlight DprE2 as a potential antimycobacterial target and provide a foundation for future exploration into the active metabolites and clinical development of pretomanid and delamanid.

摘要

结核分枝杆菌是由单一病原体引起的全球主要死亡原因之一。丙硫异烟胺和德拉马尼是两种新的抗结核药物,已通过药物发现途径取得进展。这些化合物是双环硝咪唑类化合物,作为前体药物,需要被分枝杆菌酶激活;然而,活性代谢物的确切作用机制尚不清楚。在这里,我们确定了激活丙硫异烟胺和德拉马尼的一个分子靶标:脱磷酸核糖基-2'-差向异构酶的 DprE2 亚基,这是一种合成细胞壁阿拉伯半乳聚糖所必需的酶。我们还提供了 NAD 加合物作为丙硫异烟胺的活性代谢物的证据。我们的研究结果强调了 DprE2 作为一种潜在的抗分枝杆菌靶标,并为进一步研究丙硫异烟胺和德拉马尼的活性代谢物和临床开发提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/814a/10307805/abe5f03703a7/41467_2023_39300_Fig1_HTML.jpg

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