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Locally Resolved Membrane Binding Affinity of the N-Terminus of α-Synuclein

by: Marta Robotta, Christian Hintze, Stefan Schildknecht, Niels Zijlstra, Christian Jüngst, Christiaan Karreman, Martina Huber, Marcel Leist, Vinod Subramaniam, Malte Drescher
Biochemistry, Vol. 51, No. 19. (12 April 2012), pp. 3960-3962, doi:10.1021/bi300357a  Key: citeulike:10561900

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Abstract

α-Synuclein is abundantly present in Lewy bodies, characteristic of Parkinson?s disease. Its exact physiological role has yet to be determined, but mitochondrial membrane binding is suspected to be a key aspect of its function. Electron paramagnetic resonance spectroscopy in combination with site-directed spin labeling allowed for a locally resolved analysis of the protein?membrane binding affinity for artificial phospholipid membranes, supported by a study of binding to isolated mitochondria. The data reveal that the binding affinity of the N-terminus is nonuniform.


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