Amyloid-β peptide induces mitochondrial dysfunction by inhibition of preprotein maturation.

Cell metabolism 2014 Oct 7

filter terms:

Most mitochondrial proteins possess N-terminal presequences that are required for targeting and import into the organelle. Upon import, presequences are cleaved off by matrix processing peptidases and subsequently degraded by the peptidasome Cym1/PreP, which also degrades Amyloid-beta peptides (Aβ). Here we find that impaired turnover of presequence peptides results in feedback inhibition of presequence processing enzymes. Moreover, Aβ inhibits degradation of presequence peptides by PreP, resulting in accumulation of mitochondrial preproteins and processing intermediates. Dysfunctional preprotein maturation leads to rapid protein degradation and an imbalanced organellar proteome. Our findings reveal a general mechanism by which Aβ peptide can induce the multiple diverse mitochondrial dysfunctions accompanying Alzheimer's disease. Copyright © 2014 Elsevier Inc. All rights reserved.

Citation

Dirk Mossmann, F-Nora Vögtle, Asli Aras Taskin, Pedro Filipe Teixeira, Julia Ring, Julia M Burkhart, Nils Burger, Catarina Moreira Pinho, Jelena Tadic, Desiree Loreth, Caroline Graff, Friedrich Metzger, Albert Sickmann, Oliver Kretz, Nils Wiedemann, René P Zahedi, Frank Madeo, Elzbieta Glaser, Chris Meisinger. Amyloid-β peptide induces mitochondrial dysfunction by inhibition of preprotein maturation. Cell metabolism. 2014 Oct 7;20(4):662-9