Small Molecule Inhibitors of α-Synuclein Filament Assembly†
journal contributionposted on 16.05.2006, 00:00 by Masami Masuda, Nobuyuki Suzuki, Sayuri Taniguchi, Takayuki Oikawa, Takashi Nonaka, Takeshi Iwatsubo, Shin-ichi Hisanaga, Michel Goedert, Masato Hasegawa
α-Synuclein is the major component of the filamentous inclusions that constitute defining characteristics of Parkinson's disease and other α-synucleinopathies. Here we have tested 79 compounds belonging to 12 different chemical classes for their ability to inhibit the assembly of α-synuclein into filaments in vitro. Several polyphenols, phenothiazines, porphyrins, polyene macrolides, and Congo red and its derivatives, BSB and FSB, inhibited α-synuclein filament assembly with IC50 values in the low micromolar range. Many compounds that inhibited α-synuclein assembly were also found to inhibit the formation of Aβ and tau filaments. Biochemical analysis revealed the formation of soluble oligomeric α-synuclein in the presence of inhibitory compounds, suggesting that this may be the mechanism by which filament formation is inhibited. Unlike α-synuclein filaments and protofibrils, these soluble oligomeric species did not reduce the viability of SH-SY5Y cells. These findings suggest that the soluble oligomers formed in the presence of inhibitory compounds may not be toxic to nerve cells and that these compounds may therefore have therapeutic potential for α-synucleinopathies and other brain amyloidoses.
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5YFSBpresencetau filamentsfilamentous inclusionsmicromolar rangebrain amyloidoses79 compoundspolyene macrolidesBiochemical analysisIC 50 valuesoligomeric speciesSeveral polyphenolsassemblySmall Molecule Inhibitorschemical classesSynucleinfilament formationnerve cellssynucleinopathieMany compoundssynucleinBSB