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  Metal coordination and peripheral substitution modulate the activity of cyclic tetrapyrroles on αS aggregation: A structural and cell-based study.

González, N., Gentile, I., Garro, H. A., Delgado-Ocaña, S., Ramunno, C. F., Buratti, F. A., et al. (2019). Metal coordination and peripheral substitution modulate the activity of cyclic tetrapyrroles on αS aggregation: A structural and cell-based study. Journal of Biological Inorganic Chemistry, 24(8): (in press), pp. 1269-1278. doi:10.1007/s00775-019-01711-z.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0004-9DF6-6 Version Permalink: http://hdl.handle.net/21.11116/0000-0005-49DC-2
Genre: Journal Article

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 Creators:
González, N., Author
Gentile, I., Author
Garro, H. A., Author
Delgado-Ocaña, S., Author
Ramunno, C. F., Author
Buratti, F. A., Author
Griesinger, C.1, Author              
Fernandez, C. O.1, Author              
Affiliations:
1Department of NMR Based Structural Biology, MPI for biophysical chemistry, Max Planck Society, ou_578567              

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Free keywords: Amyloid; Inhibitors; Misfolding; Neurodegeneration
 Abstract: The discovery of aggregation inhibitors and the elucidation of their mechanism of action are key in the quest to mitigate the toxic consequences of amyloid formation. We have previously characterized the antiamyloidogenic mechanism of action of sodium phtalocyanine tetrasulfonate ([Na4(H2PcTS)]) on α-Synuclein (αS), demonstrating that specific aromatic interactions are fundamental for the inhibition of amyloid assembly. Here we studied the influence that metal preferential affinity and peripheral substituents may have on the activity of tetrapyrrolic compounds on αS aggregation. For the first time, our laboratory has extended the studies in the field of the bioinorganic chemistry and biophysics to cellular biology, using a well-established cell-based model to study αS aggregation. The interaction scenario described in our work revealed that both N- and C-terminal regions of αS represent binding interfaces for the studied compounds, a behavior that is mainly driven by the presence of negatively or positively charged substituents located at the periphery of the macrocycle. Binding modes of the tetrapyrrole ligands to αS are determined by the planarity and hydrophobicity of the aromatic ring system in the tetrapyrrolic molecule and/or the preferential affinity of the metal ion conjugated at the center of the macrocyclic ring. The different capability of phthalocyanines and meso-tetra (N-methyl-4-pyridyl) porphine tetrachloride ([H2PrTPCl4]) to modulate αS aggregation in vitro was reproduced in cell-based models of αS aggregation, demonstrating unequivocally that the modulation exerted by these compounds on amyloid assembly is a direct consequence of their interaction with the target protein.

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Language(s): eng - English
 Dates: 2019-09-052019-12
 Publication Status: Published in print
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 Rev. Method: Peer
 Identifiers: DOI: 10.1007/s00775-019-01711-z
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Title: Journal of Biological Inorganic Chemistry
Source Genre: Journal
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Pages: - Volume / Issue: 24 (8) Sequence Number: (in press) Start / End Page: 1269 - 1278 Identifier: -