| Literature DB >> 29750499 |
Chia-Ju Hsieh1, John J Ferrie2, Kuiying Xu1, Iljung Lee1, Thomas J A Graham1, Zhude Tu3, Jennifer Yu4, Dhruva Dhavale4, Paul Kotzbauer4, E James Petersson2, Robert H Mach1.
Abstract
The fibrillary aggregation of the protein alpha synuclein (Asyn) is a hallmark of Parkinson's disease, and the identification of small molecule binding sites on fibrils is essential to the development of diagnostic imaging probes. A series of molecular modeling, photoaffinity labeling, mass spectrometry, and radioligand binding studies were conducted on Asyn fibrils. The results of these studies revealed the presence of three different binding sites within fibrillar Asyn capable of binding small molecules with moderate to high affinity. A knowledge of the amino acid residues in these binding sites will be important in the design of high affinity probes capable of imaging fibrillary species of Asyn.Entities:
Keywords: Alpha synuclein; Lewy bodies; Lewy neurites; Parkinson’s disease
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Year: 2018 PMID: 29750499 PMCID: PMC6736640 DOI: 10.1021/acschemneuro.8b00177
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418