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PMID: 9462863 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Lysosomes, a meeting point of proteins, chaperones, and proteases.

Journal of molecular medicine (Berlin, Germany) ·Vol. 76 ·No. 1 ·1998-01-00 ·Pages 6-12

Cuervo AM, Dice JF

Abstract

Lysosomes, classically considered as nonspecific systems for protein degradation, have recently also been shown to be able selectively to degrade specific intracellular proteins. Here we review this selective pathway of lysosomal protein degradation that involves cytosolic and intralysosomal chaperones and a receptor in the lysosomal membrane. This pathway is highly selective for cytosolic proteins containing a lysosomal targeting signal. The selective lysosomal degradation pathway is active under conditions of nutrient deprivation and plays an important role in the regulation of intracellular protein levels in stress situations. Several physiological and pathological modifications in the activity of this selective lysosomal pathway of protein degradation are discussed.

MeSH Terms
Endopeptidases/metabolism Lysosomes/metabolism Molecular Chaperones/metabolism Proteins/metabolism
Chemicals
Molecular Chaperones Proteins Endopeptidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cuervo A M
Department of Physiology, School of Medicine, Tufts University, Boston, MA 02111, USA.
Dice J F
Article Info
Journal
Journal of molecular medicine (Berlin, Germany)
Abbr.
J Mol Med (Berl)
ISSN
0946-2716
Published
1998-01-00
Pages
6-12
Language
English
Region
Germany
NLM ID
9504370
Subset
IM
Grants
NIA NIH HHS · AG06116 · United States
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