Reference : Retromer Binding to FAM21 and the WASH Complex Is Perturbed by the Parkinson Disease-...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/10993/17269
Retromer Binding to FAM21 and the WASH Complex Is Perturbed by the Parkinson Disease-Linked VPS35(D620N) Mutation.
English
McGough, Ian J. [> >]
Steinberg, Florian [> >]
Jia, Da [> >]
Barbuti, Peter A. mailto [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) >]
McMillan, Kirsty J. [> >]
Heesom, Kate J. [> >]
Caldwell, Maeve A. [> >]
Billadeau, Daniel D. [> >]
Rosen, Michael K. [> >]
Cullen, Peter J. [> >]
2014
Current Biology
Yes (verified by ORBilu)
International
0960-9822
1879-0445
[en] Retromer is a protein assembly that plays a central role in orchestrating export of transmembrane-spanning cargo proteins from endosomes into retrieval pathways destined for the Golgi apparatus and the plasma membrane [1]. Recently, a specific mutation in the retromer component VPS35, VPS35(D620N), has linked retromer dysfunction to familial autosomal dominant and sporadic Parkinson disease [2, 3]. However, the effect of this mutation on retromer function remains poorly characterized. Here we established that in cells expressing VPS35(D620N) there is a perturbation in endosome-to-TGN transport but not endosome-to-plasma membrane recycling, which we confirm in patient cells harboring the VPS35(D620N) mutation. Through comparative stable isotope labeling by amino acids in cell culture (SILAC)-based analysis of wild-type VPS35 versus the VPS35(D620N) mutant interactomes, we establish that the major defect of the D620N mutation lies in the association to the actin-nucleating Wiskott-Aldrich syndrome and SCAR homolog (WASH) complex. Moreover, using isothermal calorimetry, we establish that the primary defect of the VPS35(D620N) mutant is a 2.2 +/- 0.5-fold decrease in affinity for the WASH complex component FAM21. These data define the primary molecular defect in retromer assembly that arises from the VPS35(D620N) mutation and, by revealing functional effects on retromer-mediated endosome-to-TGN transport, provide new insight into retromer deregulation in Parkinson disease.
http://hdl.handle.net/10993/17269
Copyright (c) 2014 The Authors. Published by Elsevier Inc. All rights reserved.

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