Marine Drugs (Oct 2017)

Discovering the Biological Target of 5-epi-Sinuleptolide Using a Combination of Proteomic Approaches

  • Elva Morretta,
  • Roberta Esposito,
  • Carmen Festa,
  • Raffaele Riccio,
  • Agostino Casapullo,
  • Maria Chiara Monti

DOI
https://doi.org/10.3390/md15100312
Journal volume & issue
Vol. 15, no. 10
p. 312

Abstract

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Sinuleptolide and its congeners are diterpenes with a norcembranoid skeleton isolated from the soft coral genus Sinularia. These marine metabolites are endowed with relevant biological activities, mainly associated with cancer development. 5-epi-sinuleptolide has been selected as a candidate for target discovery studies through the application of complementary proteomic approaches. Specifically, a combination of conventional chemical proteomics based on affinity chromatography, coupled with high-resolution mass spectrometry and bioinformatics, as well as drug affinity responsive target stability (DARTS), led to a clear identification of actins as main targets for 5-epi-sinuleptolide. Subsequent in-cell assays, performed with cytochalasin D as reference compound, gave information on the ability of 5-epi-sinuleptolide to disrupt the actin cytoskeleton by loss of actin fibers and formation of F-actin amorphous aggregates. These results suggest the potential application of 5-epi-sinuleptolide as a useful tool in the study of the molecular processes impaired in several disorders in which actin is thought to play an essential role.

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