Chemical Synthesis of Alpha‐Synuclein Proteins via Solid‐Phase Peptide Synthesis and Native Chemical Ligation

Author:

Gatzemeier Luisa Maria12ORCID,Meyer Franc3ORCID,Diederichsen Ulf1,Outeiro Tiago Fleming2456ORCID

Affiliation:

1. Institute of Organic and Biomolecular Chemistry Georg-August-University Göttingen Tammannstraße 2 37077 Göttingen Germany

2. Department of Experimental Neurodegeneration Center for Biostructural Imaging of Neurodegeneration University Medical Center Göttingen Waldweg 33 37073 Göttingen Germany

3. Institute of Inorganic Chemistry Georg-August-University Göttingen Tammannstraße 4 37077 Göttingen Germany

4. Max Planck Institute for Multidisciplinary Sciences Hermann-Rein-Straße 3 37075 Göttingen Germany

5. Translational and Clinical Research Institute Faculty of Medical Sciences Newcastle University Framlington Place Newcastle Upon Tyne NE2 4HH UK

6. Scientific employee with an honorary contract at Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) Von-Siebold-Straße 3a 37075 Göttingen Germany

Abstract

AbstractAlpha‐Synuclein (α‐Synuclein) is a 140 amino acid protein implicated in neurodegenerative disorders known as synucleinopathies, where it accumulates in proteinaceous inclusions in the brain. The normal physiological function of α‐Synuclein remains obscure, as it exists in several non‐neuronal cells in which its function has not been studied. Given the tremendous interest in studying α‐Synuclein, and the existing limitations in the production of modified forms of the protein, we developed a method for the chemical synthesis of α‐Synuclein by combining peptide fragment synthesis via automated microwave‐assisted solid‐phase peptide synthesis and ligation strategies. Our synthetic pathway enables the synthesis of protein variants of interest, carrying either mutations or posttranslational modifications, for further investigations of the effects on the structure and aggregation behavior of the protein. Ultimately, our study forms the foundation for future syntheses and studies of other custom‐made α‐Synuclein variants with a single or several modifications, as necessary.

Funder

Deutsche Forschungsgemeinschaft

Georg-August-Universität Göttingen

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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