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PMID: 2995355 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A soluble ATP-dependent system for protein degradation from murine erythroleukemia cells. Evidence for a protease which requires ATP hydrolysis but not ubiquitin.

The Journal of biological chemistry ·Vol. 260 ·No. 22 ·1985-10-05 ·Pages 11994-2000

Waxman L, Fagan JM, Tanaka K, Goldberg AL

Abstract

A soluble ATP-dependent system for protein degradation has been demonstrated in reticulocyte lysates, but not in extracts of nucleated cells. We report that extracts of undifferentiated murine erythroleukemia (MEL) cells contain a labile ATP-stimulated proteolytic system. The addition of ATP to MEL cell extracts at alkaline pH enhances degradation of endogenous cell proteins and various radiolabeled exogenous polypeptides from 2-15-fold. Nonhydrolyzable ATP analogs had no effect. In reticulocytes, one role of ATP in proteolysis is for ubiquitin conjugation to protein substrates. MEL cells also contain ubiquitin and extracts can conjugate 125I-ubiquitin to cell proteins; however, this process in MEL cells seems unrelated to protein breakdown. After removal of ubiquitin from these extracts by DEAE- or gel chromatography, the stimulation of proteolysis by ATP was maintained and readdition of purified ubiquitin had no further effect. In addition, these extracts degraded in an ATP-dependent fashion casein whose amino groups were blocked and could not be conjugated to ubiquitin. After gel filtration or DEAE-chromatography of the MEL cell extracts (unlike those from reticulocytes), we isolated a high molecular weight (600,000) ATP-dependent proteolytic activity, which exhibits many of the properties of energy-dependent proteolysis seen in crude cell extracts. For example, both the protease and crude extracts are inhibited by hemin and N-ethylmaleimide and both hydrolyze casein, globin, and lysozyme rapidly and denatured albumin relatively slowly. The protease, like the crude extracts, is also stimulated by UTP, CTP, and GTP, although not as effectively as ATP. Also, nonhydrolyzable ATP analogs and pyrophosphate do not stimulate the protease. Thus, some mammalian cells contain a cytosolic proteolytic pathway that appears independent of ubiquitin and involves and ATP-dependent protease, probably similar to that found in Escherichia coli or mitochondria.

MeSH Terms
Adenosine Triphosphate/metabolism,pharmacology Adenylyl Imidodiphosphate/pharmacology Animals Cell Line Ethylmaleimide/pharmacology Heme/pharmacology High Mobility Group Proteins/pharmacology Isoflurophate/pharmacology Kinetics Leukemia, Erythroblastic, Acute/enzymology Leukemia, Experimental/enzymology Mice Peptide Hydrolases/metabolism Proteins/metabolism Rabbits Reticulocytes/enzymology Ubiquitins/pharmacology
Chemicals
High Mobility Group Proteins Proteins Ubiquitins Isoflurophate Adenylyl Imidodiphosphate Heme Adenosine Triphosphate Peptide Hydrolases Ethylmaleimide
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Waxman L
Fagan J M
Tanaka K
Goldberg A L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1985-10-05
Pages
11994-2000
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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