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Amyloid-beta Peptide Induces Mitochondrial Dysfunction by Inhibition of Preprotein Maturation

Mossmann, Dirk (author)
Voegtle, F-Nora (author)
Taskin, Asli Aras (author)
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Teixeira, Pedro Filipe (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Ring, Julia (author)
Burkhart, Julia M. (author)
Burger, Nils (author)
Pinho, Catarina Moreira (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Tadic, Jelena (author)
Loreth, Desiree (author)
Graff, Caroline (author)
Karolinska Institutet
Metzger, Friedrich (author)
Sickmann, Albert (author)
Kretz, Oliver (author)
Wiedemann, Nils (author)
Zahedi, Rene P. (author)
Madeo, Frank (author)
Glaser, Elzbieta (author)
Stockholms universitet,Institutionen för biokemi och biofysik
Meisinger, Chris (author)
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 (creator_code:org_t)
Elsevier BV, 2014
2014
English.
In: Cell Metabolism. - : Elsevier BV. - 1550-4131 .- 1932-7420. ; 20:4, s. 662-669
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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 (A beta). Here we find that impaired turnover of presequence peptides results in feedback inhibition of presequence processing enzymes. Moreover, A beta 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 A beta peptide can induce the multiple diverse mitochondrial dysfunctions accompanying Alzheimer's disease.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

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