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PMID: 1089651 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Degradation of abnormal proteins in Escherichia coli. Formation of protein inclusions in cells exposed to amino acid analogs.

The Journal of biological chemistry ·Vol. 250 ·No. 3 ·1975-02-10 ·Pages 1112-22

Prouty WF, Karnovsky MJ, Goldberg AL

Abstract

Cells of Escherichia coli selectively degrade proteins that have incorporated amino acid analogs. Within 1 hour after exposure of cells to canavanine, 50% of the analog-containing proteins were degraded to acid-soluble form. At the same time, no net loss of canavanine-containing protein occurred from the 100,000 X g supernatant. Instead, most of the proteins containing the analog, unlike normal ones, accumulated in particulate fractions sedimenting at 10,000 X g or 100,000 X g. They were then lost from these fractions concomitant with the degradation of the abnormal proteins. The loss of such proteins from particulate fractions accounted for all of the protein degraded to acid-soluble form. Similar observations were obtained after incorporation of other analogs or puromycin. The 10,000 X g pellets correspond to amorphous dense intracellular granules visible in electron micrographs of cells exposed to canavanine. Upon removal of the analog, these granules disappeared, simultaneously with the degradation of the analog-containing proteins. These pellets do not resemble a degradative organelle, like the lysosome; they are not osmotically sensitive, do not exclude inulin, are not enclosed by a membrane, and do not show autolytic activity. The proteins in the granules could be solubilized by sodium dodecyl sulfate but not by Triton, NaC1, dithiothreitol, RNase, DNase, or phospholipase. The proteins extracted from the pellet with sodium dodecyl sulfate tend to become particulate again upon removal of this detergent. Incorporation of canavanine caused a normally soluble polypeptide, the monomer of beta-galactosidase, to be inactive and found in the sedimentable fraction. These findings suggest that (a) the presence of amino acid analogs in proteins can make them less soluble, and (b) the inclusions are formed by the spontaneous precipitation of abnormal proteins rather than by an active granule-forming process.

MeSH Terms
Amino Acids/metabolism Bacterial Proteins/metabolism Dithiothreitol/pharmacology Electrophoresis, Polyacrylamide Gel Escherichia coli/drug effects,metabolism,ultrastructure Inulin/metabolism Kinetics Leucine/metabolism Microscopy, Electron Muramidase Phospholipases Polyethylene Glycols/pharmacology Pronase Sodium Dodecyl Sulfate/pharmacology Solubility Spheroplasts/metabolism Structure-Activity Relationship Subcellular Fractions/metabolism Time Factors Trypsin
Chemicals
Amino Acids Bacterial Proteins Sodium Dodecyl Sulfate Polyethylene Glycols Inulin Phospholipases Muramidase Trypsin Pronase Leucine Dithiothreitol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Prouty W F
Karnovsky M J
Goldberg A L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1975-02-10
Pages
1112-22
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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