Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1997 May;29(5):365-85.
doi: 10.1023/a:1026486801018.

Autophagic proteolysis: control and specificity

Affiliations
Review

Autophagic proteolysis: control and specificity

E F Blommaart et al. Histochem J. 1997 May.

Abstract

The rate of proteolysis is an important determinant of the intracellular protein content. Part of the degradation of intracellular proteins occurs in the lysosomes and is mediated by macroautophagy. In liver, macroautophagy is very active and almost completely accounts for starvation-induced proteolysis. Factors inhibiting this process include amino acids, cell swelling and insulin. In the mechanisms controlling macroautophagy, protein phosphorylation plays an important role. Activation of a signal transduction pathway, ultimately leading to phosphorylation of ribosomal protein S6, accompanies inhibition of macroautophagy. Components of this pathway may include a heterotrimeric Gi3-protein, phosphatidylinositol 3-kinase and p70S6 kinase. Recent evidence indicates that lysosomal protein degradation can be selective and occurs via ubiquitin-dependent and -independent pathways.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Chem Biol Interact. 1976 Apr;13(1):77-87 - PubMed
    1. Am J Physiol. 1992 Apr;262(4 Pt 1):C1031-8 - PubMed
    1. Biochem J. 1992 Jun 15;284 ( Pt 3):633-6 - PubMed
    1. J Cell Biol. 1992 Jul;118(2):301-8 - PubMed
    1. Annu Rev Biochem. 1992;61:761-807 - PubMed

Publication types

MeSH terms

LinkOut - more resources