Structure of Parkin Reveals Mechanisms for Ubiquitin Ligase Activation

Author:

Trempe Jean-François1,Sauvé Véronique2,Grenier Karl1,Seirafi Marjan2,Tang Matthew Y.1,Ménade Marie2,Al-Abdul-Wahid Sameer2,Krett Jonathan1,Wong Kathy2,Kozlov Guennadi2,Nagar Bhushan2,Fon Edward A.1,Gehring Kalle2

Affiliation:

1. McGill Parkinson Program, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montréal, Québec H3A 2B4, Canada.

2. Groupe de Recherche Axé sur la Structure des Protéines and Department of Biochemistry, McGill University, Montréal, Québec H3G 1Y6, Canada.

Abstract

Parkin Enhanced? Inactivation of parkin, an E3 ubiquitin ligase, is responsible for a familial form of Parkinson's disease and may be involved in sporadic forms as well. Trempe et al. (p. 1451 , published online 9 May) present the crystal structure of full-length parkin in an autoinhibited configuration. Guided by the structure, mutations were designed that activated parkin both in vitro and in cells. Because parkin is neuroprotective, the structure provides a framework for enhancing parkin function as a therapeutic strategy in Parkinson's disease.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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