Linking bioactive compounds to their cellular targets is a central challenge in chemical biology. Herein we report the mode of action of perthamide C, a natural cyclopeptide isolated from the marine sponge Theonella swinhoei. Through an emerging mass spectrometry-based chemical proteomics approach, Heat Shock Protein 90 and Glucose Regulated Protein 94 were identified as key targets of perthamide C and this evidence has been validated using surface plasmon resonance. The ability of perthamide C to influence heat shock protein-mediated cell apoptosis revealed that this marine metabolite could be a good candidate for the development of a lead compound with therapeutic applications based on apoptosis modulation.
Chemical Proteomics Reveals Bolinaquinone as a Clathrin-Mediated Endocytosis Inhibitor / Margarucci, Luigi; Monti, Maria Chiara; Fontanella, Bianca; Riccio, Raffaele; Casapullo, Agostino. - In: MOLECULAR BIOSYSTEMS. - ISSN 1742-206X. - 7:(2011), pp. 480-485. [10.1039/c0mb00126k]
Chemical Proteomics Reveals Bolinaquinone as a Clathrin-Mediated Endocytosis Inhibitor
MONTI, Maria Chiara;FONTANELLA, BIANCA;RICCIO, Raffaele;CASAPULLO, Agostino
2011
Abstract
Linking bioactive compounds to their cellular targets is a central challenge in chemical biology. Herein we report the mode of action of perthamide C, a natural cyclopeptide isolated from the marine sponge Theonella swinhoei. Through an emerging mass spectrometry-based chemical proteomics approach, Heat Shock Protein 90 and Glucose Regulated Protein 94 were identified as key targets of perthamide C and this evidence has been validated using surface plasmon resonance. The ability of perthamide C to influence heat shock protein-mediated cell apoptosis revealed that this marine metabolite could be a good candidate for the development of a lead compound with therapeutic applications based on apoptosis modulation.File | Dimensione | Formato | |
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