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Nannocystin A: an Elongation Factor 1 Inhibitor from Myxobacteria with Differential Anti‐Cancer Properties
Authors:Philipp Krastel  Silvio Roggo  Markus Schirle  Nathan T Ross  Francesca Perruccio  Peter Aspesi Jr  Thomas Aust  Kathrin Buntin  David Estoppey  Brigitta Liechty  Felipa Mapa  Klaus Memmert  Howard Miller  Xuewen Pan  Ralph Riedl  Christian Thibaut  Jason Thomas  Trixie Wagner  Eric Weber  Xiaobing Xie  Esther K Schmitt  Dr Dominic Hoepfner
Affiliation:1. Novartis Institutes for BioMedical Research, Novartis Campus, 4056 Basel (Switzerland);2. Novartis Institutes for BioMedical Research, 250 Massachusetts Avenue, Cambridge, MA 02139 (USA)
Abstract:Cultivation of myxobacteria of the Nannocystis genus led to the isolation and structure elucidation of a class of novel cyclic lactone inhibitors of elongation factor 1. Whole genome sequence analysis and annotation enabled identification of the putative biosynthetic cluster and synthesis process. In biological assays the compounds displayed anti‐fungal and cytotoxic activity. Combined genetic and proteomic approaches identified the eukaryotic translation elongation factor 1α (EF‐1α) as the primary target for this compound class. Nannocystin A ( 1 ) displayed differential activity across various cancer cell lines and EEF1A1 expression levels appear to be the main differentiating factor. Biochemical and genetic evidence support an overlapping binding site of 1 with the anti‐cancer compound didemnin B on EF‐1α. This myxobacterial chemotype thus offers an interesting starting point for further investigations of the potential of therapeutics targeting elongation factor 1.
Keywords:didemnin   B  elongation factor 1α    myxobacteria  nannocystin   A  natural products
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