Ipomoeassin F Binds Sec61 alpha to Inhibit Protein Translocation

by Zong, G. H.; Hu, Z. J.; O'Keefe, S.; Tranter, D.; Iannotti, M. J.; Baron, L.; Hall, B.; Corfield, K.; Paatero, A. O.; Henderson, M. J.; Roboti, P.; Zhou, J. H.; Sun, X. W.; Govindarajan, M.; Rohde, J. M.; Blanchard, N.; Simmonds, R.; Inglese, J.; Du, Y. C

Ipomoeassin F is a potent natural cytotoxin that inhibits growth of many tumor cell lines with single-digit nanomolar potency. However, its biological and pharmacological properties have remained largely unexplored. Building upon our earlier achievements in total synthesis and medicinal chemistry, we used chemical proteomics to identify Sec61 alpha (protein transport protein Sec61 subunit alpha isoform 1), the pore-forming subunit of the Sec61 protein translocon, as a direct binding partner of ipomoeassin F in living cells. The interaction is specific and strong enough to survive lysis conditions, enabling a biotin analogue of ipomoeassin F to pull down Sec61 alpha from live cells, yet it is also reversible, as judged by several experiments including fluorescent streptavidin staining, delayed competition in affinity pulldown, and inhibition of TNF biogenesis after washout. Sec61 alpha forms the central subunit of the ER protein translocation complex, and the binding of ipomoeassin F results in a substantial, yet selective, inhibition of protein translocation in vitro and a broad ranging inhibition of protein secretion in live cells. Lastly, the unique resistance profile demonstrated by specific amino acid single-point mutations in Sec61 alpha provides compelling evidence that Sec61 alpha is the primary molecular target of ipomoeassin F and strongly suggests that the binding of this natural product to Sec61 alpha is distinctive. Therefore, ipomoeassin F represents the first plant-derived, carbohydrate-based member of a novel structural class that offers new opportunities to explore Sec61 alpha function and to further investigate its potential as a therapeutic target for drug discovery.

Journal
Journal of the American Chemical Society
Volume
141
Issue
21
Year
2019
Start Page
8450-8461
URL
https://dx.doi.org/10.1021/jacs.8b13506
ISBN/ISSN
1520-5126; 0002-7863
DOI
10.1021/jacs.8b13506