Regulation of Aggregation Behavior and Neurotoxicity of Prion Neuropeptides by Platinum Complexes

• Published in: Inorganic chemistry Vol. 53; no. 10; pp. 5044 - 5054
• Main Authors: Wang, Xuesong, Cui, Menghan, Zhao, Cong, He, Lei, Zhu, Dengsen, Wang, Baohuai, Du, Weihong
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 19.05.2014
• Subjects: Carboplatin - chemical synthesis; Carboplatin - chemistry; Carboplatin - pharmacology; Cell Line, Tumor; Cell Survival - drug effects; Cisplatin - chemical synthesis; Cisplatin - chemistry; Cisplatin - pharmacology; Dose-Response Relationship, Drug; Humans; Molecular Structure; Organoplatinum Compounds - chemical synthesis; Organoplatinum Compounds - chemistry; Organoplatinum Compounds - pharmacology; Prions - antagonists & inhibitors; Prions - metabolism; Protein Aggregates - drug effects; Structure-Activity Relationship
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic500092t

Prion diseases belong to a group of infectious, fatal neurodegenerative disorders. The conformational conversion of a cellular prion protein (PrPC) into an abnormal misfolded isoform (PrPSc) is the key event in prion disease pathology. PrP106–126 resembles PrPSc in some physicochemical and biological characteristics, such as apoptosis induction in neurons, fibrillar formation, and mediation of the conversion of native cellular PrPC to PrPSc. Numerous studies have been conducted to explore the inhibiting methods on the aggregation and neurotoxicity of prion neuropeptide PrP106–126. We showed that PrP106–126 aggregation, as assessed by fluorescence assay and atomic force microscopy, is inhibited by platinum complexes cisplatin, carboplatin, and Pt­(bpy)­Cl2. ESI-MS and NMR assessments of PrP106–126 and its mutant peptides demonstrate that platinum complexes bind to the peptides in coordination and nonbonded interactions, which rely on the ligand properties and the peptide sequence. In peptides, methionine residue is preferred as a potent binding site over histidine residue for the studied platinum complexes, implying a typical thiophile characteristic of platinum. The neurotoxicity induced by PrP106–126 is better inhibited by Pt­(bpy)­Cl2 and cisplatin. Furthermore, the ligand configuration contributes to both the binding affinity and the inhibition of peptide aggregation. The pursuit of novel platinum candidates that selectively target prion neuropeptide is noteworthy for medicinal inorganic chemistry and chemical biology.