A Potent Sybody Selectively Inhibits α-Synuclein Amyloid Formation by Binding to the P1 Region

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Abstract

Increasing research efforts focus on exploiting antibodies to inhibit the amyloid formation of neurodegenerative proteins. Nevertheless, it is challenging to discover antibodies that inhibit this process in a specific manner. Using ribosome display, we screened for synthetic single-domain antibodies, i.e., sybodies, of the P1 region of α-synuclein (residues 36-42), a protein that forms amyloid in Parkinson’s disease and multiple-system atrophy. Hits were assessed for direct binding to a P1 peptide and the inhibition of amyloid formation. We discovered a sybody, named αSP1, that inhibits amyloid formation of α-synuclein at substoichiometric concentrations in a specific manner, even within highly crowded heterogeneous mixtures. Fluorescence resonance energy transfer-based binding assays and seeding experiments with and without αSP1 further demonstrate the importance of the P1 region for both primary and secondary nucleation mechanisms of amyloid assembly.

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Gialama, D., Vadukul, D. M., Thrush, R. J., Radford, S. E., & Aprile, F. A. (2024). A Potent Sybody Selectively Inhibits α-Synuclein Amyloid Formation by Binding to the P1 Region. Journal of Medicinal Chemistry, 67(12), 9857–9868. https://doi.org/10.1021/acs.jmedchem.3c02408

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