http://www.cnr.it/ontology/cnr/individuo/prodotto/ID58785
Bioinorganic Chemistry of Parkinson's Disease: Structural Determinants for the Copper-Mediated Amyloid Formation of Alpha-Synuclein (Articolo in rivista)
- Type
- Label
- Bioinorganic Chemistry of Parkinson's Disease: Structural Determinants for the Copper-Mediated Amyloid Formation of Alpha-Synuclein (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ic1016752 (literal)
- Alternative label
Binolfi, Andres; Rodriguez, Esau E.; Valensin, Daniela; D'Amelio, Nicola; Ippoliti, Emiliano; Obal, Gonzalo; Duran, Rosario; Magistrato, Alessandra; Pritsch, Otto; Zweckstetter, Markus; Valensin, Gianni; Carloni, Paolo; Quintanar, Liliana; Griesinger, Chr (2010)
Bioinorganic Chemistry of Parkinson's Disease: Structural Determinants for the Copper-Mediated Amyloid Formation of Alpha-Synuclein
in Inorganic chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Binolfi, Andres; Rodriguez, Esau E.; Valensin, Daniela; D'Amelio, Nicola; Ippoliti, Emiliano; Obal, Gonzalo; Duran, Rosario; Magistrato, Alessandra; Pritsch, Otto; Zweckstetter, Markus; Valensin, Gianni; Carloni, Paolo; Quintanar, Liliana; Griesinger, Chr (literal)
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- ISI Web of Science (WOS) (literal)
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- 1. Univ Nacl Rosario, Inst Biol Mol & Celular Rosario, Consejo Nacl Invest Cient & Tecn, RA-2000 Rosario, Santa Fe, Argentina
2. Ctr Invest & Estudios Avanzados Cinvestav, Mexico City 07360, DF, Mexico
3. Univ Siena, Dipartimento Chim, I-53100 Siena, Italy
4. Bracco Imaging CRB Trieste, I-34149 Trieste, Italy
5. CNR IOM Democritos Natl Simulat Ctr, I-34014 Trieste, Italy
6. Int Sch Adv Studies SISSA ISAS, I-34014 Trieste, Italy
7. Inst Pasteur Montevideo, Montevideo 11400, Uruguay
8. Max Planck Inst Biophys Chem, Dept NMR Based Struct Biol, D-37077 Gottingen, Germany
9. DFG Res Ctr Mol Physiol Brain CMPB, Gottingen, Germany (literal)
- Titolo
- Bioinorganic Chemistry of Parkinson's Disease: Structural Determinants for the Copper-Mediated Amyloid Formation of Alpha-Synuclein (literal)
- Abstract
- The aggregation of alpha-synuclein (AS) is a critical step in the etiology of Parkinson's disease (PD). A central, unresolved question in the pathophysiology of PD relates to the role of AS-metal interactions in amyloid fibril formation and neurodegeneration. Our previous works established a hierarchy in alpha-synuclein-metal ion interactions, where Cu(II) binds specifically to the protein and triggers its aggregation under conditions that might be relevant for the development of PD. Two independent, non-interacting copper-binding sites were identified at the N-terminal region of AS, with significant difference in their affinities for the metal ion. In this work we have solved unknown details related to the structural binding specificity and aggregation enhancement mediated by Cu(II). The high-resolution structural characterization of the highest affinity N-terminus AS-Cu(II) complex is reported here. Through the measurement of AS aggregation kinetics we proved conclusively that the copper-enhanced AS amyloid formation is a direct consequence of the formation of the AS-Cu(II) complex at the highest affinity binding site. The kinetic behavior was not influenced by the His residue at position 50, arguing against an active role for this residue in the structural and biological events involved in the mechanism of copper-mediated AS aggregation. These new findings are central to elucidate the mechanism through which the metal ion participates in the fibrillization of AS and represent relevant progress in the understanding of the bionorganic chemistry of PD. (literal)
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