Abstract
α-Synuclein is the aggregation-prone protein associated with Parkinson’s disease (PD) and related neurodegenerative diseases. Complicating both its biological functions and toxic aggregation are a variety of posttranslational modifications. These modifications have the potential to either positively or negatively affect α-synuclein aggregation, raising the possibility that the enzymes that add or remove these modifications could be therapeutic targets in PD. Synthetic protein chemistry is uniquely positioned to generate site-specifically and homogeneously modified proteins for biochemical study. Here, we review the application of synthetic peptides and proteins towards understanding the effects of α-synuclein posttranslational modifications.
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Pratt, M. R., Abeywardana, T., & Marotta, N. P. (2015, July 7). Synthetic proteins and peptides for the direct interrogation of α-synuclein posttranslational modifications. Biomolecules. MDPI AG. https://doi.org/10.3390/biom5031210
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