Insight into the mode of action of the LRRK2 Y1699C pathogenic mutant

Daniëls, V., Vancraenenbroeck, R., Law, B.M.H., Greggio, E., Lobbestael, E., Gao, F., De Maeyer, M., Cookson, M.R., Harvey, K., Baekelandt, V. and Taymans, J-M. (2010) Insight into the mode of action of the LRRK2 Y1699C pathogenic mutant. Journal of Neurochemistry, 116 (2). pp. 304-315. 10.1111/j.1471-4159.2010.07105.x.

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DOI: 10.1111/j.1471-4159.2010.07105.x

Abstract

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most prevalent known cause of autosomal dominant Parkinson's disease. The LRRK2 gene encodes a Roco protein featuring a Ras of complex proteins (ROC) GTPase and a kinase domain linked by the C-terminal of ROC (COR) domain. Here, we explored the effects of the Y1699C pathogenic LRRK2 mutation in the COR domain on GTPase activity and interactions within the catalytic core of LRRK2. We observed a decrease in GTPase activity for LRRK2 Y1699C comparable to the decrease observed for the R1441C pathogenic mutant and the T1348N dysfunctional mutant. To study the underlying mechanism, we explored the dimerization in the catalytic core of LRRK2. ROC-COR dimerization was significantly weakened by the Y1699C or R1441C/G mutation. Using a competition assay, we demonstrated that the intra-molecular ROC: COR interaction is favoured over ROC: ROC dimerization. Interestingly, the intra-molecular ROC: COR interaction was strengthened by the Y1699C mutation. This is supported by a 3D homology model of the ROC-COR tandem of LRRK2, showing that Y1699 is positioned at the intra-molecular ROC: COR interface. In conclusion, our data provides mechanistic insight into the mode of action of the Y1699C LRRK2 mutant: the Y1699C substitution, situated at the intra-molecular ROC: COR interface, strengthens the intra-molecular ROC: COR interaction, thereby locally weakening the dimerization of LRRK2 at the ROC-COR tandem domain resulting in decreased GTPase activity

Item Type:Article
Uncontrolled Keywords:dimerization; GTPase; leucine-rich repeat kinase 2; Parkinson's disease
Departments, units and centres:Department of Pharmacology > Department of Pharmacology
ID Code:2777
Journal or Publication Title:Journal of Neurochemistry
Deposited By:Library Staff
Deposited On:10 Feb 2012 09:18
Last Modified:10 Feb 2012 09:18

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