Identification of Mortalin as the Main Interactor of Mycalin A, a Poly-Brominated C-15 Acetogenin Sponge Metabolite, by MS-Based Proteomics.
Elva MorrettaAlessandra CapuanoGilda D'UrsoAntonia VoliMatteo MozzicafreddoSonia Di GaetanoDomenica CapassoMarina SalaMaria Carmina ScalaPietro CampigliaVincenzo PiccialliAgostino CasapulloPublished in: Marine drugs (2024)
Mycalin A (MA) is a polybrominated C-15 acetogenin isolated from the marine sponge Mycale rotalis . Since this substance displays a strong antiproliferative bioactivity towards some tumour cells, we have now directed our studies towards the elucidation of the MA interactome through functional proteomic approaches, (DARTS and t-LIP-MS). DARTS experiments were performed on Hela cell lysates with the purpose of identifying MA main target protein(s); t-LiP-MS was then applied for an in-depth investigation of the MA-target protein interaction. Both these techniques exploit limited proteolysis coupled with MS analysis. To corroborate LiP data, molecular docking studies were performed on the complexes. Finally, biological and SPR analysis were conducted to explore the effect of the binding. Mortalin (GRP75) was identified as the MA's main interactor. This protein belongs to the Hsp70 family and has garnered significant attention due to its involvement in certain forms of cancer. Specifically, its overexpression in cancer cells appears to hinder the pro-apoptotic function of p53, one of its client proteins, because it becomes sequestered in the cytoplasm. Our research, therefore, has been focused on the possibility that MA might prevent this sequestration, promoting the re-localization of p53 to the nucleus and facilitating the apoptosis of tumor cells.
Keyphrases
- mass spectrometry
- molecular docking
- cell cycle arrest
- multiple sclerosis
- ms ms
- cell death
- endoplasmic reticulum stress
- induced apoptosis
- protein protein
- oxidative stress
- molecular dynamics simulations
- amino acid
- cell proliferation
- squamous cell carcinoma
- label free
- stem cells
- heat shock protein
- machine learning
- papillary thyroid
- big data
- squamous cell
- mesenchymal stem cells
- transcription factor
- bone marrow
- cell therapy
- heat shock