How Acrolein and Copper Influence a Brain Protein

  • Author: Chemistry – A European Journal
  • Published Date: 29 March 2020
  • Source / Publisher: Chemistry – A European Journal/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: How Acrolein and Copper Influence a Brain Protein

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Parkinson's disease and other neurodegenerative disorders affect millions of people worldwide, but the exact reason for their onset is still unknown. Several factors may be involved, such as oxidative stress, dysregulation of metal ions (especially copper ions), and the abnormal aggregation of α-synuclein (pictured), an intrinsically disordered protein found in brain tissue. How these factors are correlated to each other is an open question.


Valentina Oliveri, Università degli Studi di Catania, Italy, Francesco Bellia, Institute of Crystallography, Consiglio Nazionale delle Ricerche (CNR), Catania, Italy, Peter Faller, University of Strasbourg, France, and colleagues have investigated the combined effects of copper ions and the reactive carbonyl species acrolein (ACR) on the structure and function of α-synuclein. The team used several techniques to monitor the changes induced by Cu2+ and acrolein, including ultra-performance liquid chromatography coupled with high-resolution mass spectrometry (UPLC-MS), dynamic light scattering, and spectroscopic and fluorescence assays.


The team found that copper and acrolein compete with each other to target a histidine residue of α-synuclein. Copper can bind to the protein at different sites, while acrolein forms Michael adducts or Schiff bases (pictured below; Cu2+‐binding sites on top, acrolein adducts on the bottom). These changes can affect the formation of aggregates of α-synuclein. According to the researchers, the potential synergistic effects of these two factors might play a role in the onset and progression of Parkinson's disease and related diseases.

 


 

 

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Magazine of Chemistry Europe (16 European Chemical Societies)published by Wiley-VCH