| Literature DB >> 24070323 |
Thai Leong Yap1, James M Gruschus, Arash Velayati, Ellen Sidransky, Jennifer C Lee.
Abstract
Mutations in GBA1, the gene for glucocerebrosidase (GCase), are genetic risk factors for Parkinson disease (PD). α-Synuclein (α-Syn), a protein implicated in PD, interacts with GCase and efficiently inhibits enzyme activity. GCase deficiency causes the lysosomal storage disorder Gaucher disease (GD). We show that saposin C (Sap C), a protein vital for GCase activity in vivo, protects GCase against α-syn inhibition. Using nuclear magnetic resonance spectroscopy, site-specific fluorescence, and Förster energy transfer probes, Sap C was observed to displace α-syn from GCase in solution and on lipid vesicles. Our results suggest that Sap C might play a crucial role in GD-related PD.Entities:
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Year: 2013 PMID: 24070323 PMCID: PMC3833811 DOI: 10.1021/bi401191v
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162