Chemische Biologie, Universität Duisburg-Essen, ZMB, Fakultät für Biologie, Universitätsstr. 2, 45117, Essen, Germany.
Department of Dermatology, University hospital Essen, West German Cancer Center, University Duisburg-Essen and the German Cancer Consortium (DKTK).
Chemistry. 2020 Jul 14;26(39):8524-8531. doi: 10.1002/chem.202001577. Epub 2020 Jun 17.
Natural products (NPs) are an important inspirational source for developing drugs and chemical probes. In 1999, the group of Ōmura reported the constitutional elucidation of zelkovamycin. Although largely unrecognized so far, this NP displays structural similarities as well as differences to the argyrin NP family, a class of peptidic NPs with promising anticancer activities and diverse mode-of-action at the molecular level. By a combination of structure elucidation experiments, the first total synthesis of zelkovamycin and bioassays, the zelkovamycin configuration was determined and its previously proposed molecular structure was revised. The full structure assignment proves zelkovamycin as an additional member of the argyrins with however unique OXPHOS inhibitory properties. Zelkovamycin may therefore not only serve as a new starting point for chemical inhibitors of the OXPHOS system, but also guide customized argyrin NP isolation and biosynthesis studies.
天然产物(NPs)是开发药物和化学探针的重要灵感来源。1999 年,大村智课题组报道了泽拉霉素的结构阐明。尽管到目前为止还没有得到广泛的认可,但这种 NP 与 Argirins NP 家族在结构上既有相似之处,也有不同之处,Argirins NP 是一类具有 promising anticancer activities 的肽类 NPs,在分子水平上具有多种作用模式。通过结构阐明实验、泽拉霉素的首次全合成和生物测定的结合,确定了泽拉霉素的构型,并对其之前提出的分子结构进行了修正。完整的结构分配证明泽拉霉素是 Argirins 的一个额外成员,但具有独特的 OXPHOS 抑制特性。因此,泽拉霉素不仅可以作为 OXPHOS 系统化学抑制剂的新起点,还可以指导定制的 Argirins NP 分离和生物合成研究。