Abstract
Carboplatin (CPT), today the most important platinum(II) anticancer drug, manifests an extreme kinetic inertness, in vitro, at physiological pH; the actual mechanisms for its activation inside cells are still poorly understood. We show here that horse heart cytochrome c reacts with CPT, leading to the formation of stable platinum/protein adducts. The two major CPT-cytochrome c species resulting from the aforementioned reaction were characterised by electrospray ionisation mass spectrometry (ESI-MS). Notably, both these adducts have the ability to react with guanosine 5'-monophosphate (5'-GMP), giving rise to the respective cytochrome c-CPT-5'-GMP ternary complexes. Additional ESI-MS measurements on enzymatically cleaved cytochrome c adducts suggest that protein platination probably occurs at Met65. The mechanistic implications of these findings are discussed.
Original language | English |
---|---|
Pages (from-to) | 755-764 |
Number of pages | 10 |
Journal | Journal of biological inorganic chemistry |
Volume | 13 |
Issue number | 5 |
DOIs | |
Publication status | Published - Jun-2008 |
Externally published | Yes |
Keywords
- carboplatin
- cytochrome c
- electrospray ionisation mass spectrometry
- metallodrugs
- mechanism of action
- ANTICANCER DRUG CARBOPLATIN
- MASS-SPECTROMETRY
- CONTAINING PEPTIDES
- BINDING-SITES
- CISPLATIN
- PLATINUM
- KINETICS
- HYDROLYSIS
- METHIONINE
- OXALIPLATIN