Abstract
The mechanism of inhibition of Moloney leukemia virus by N-methylisatin-beta-4',4'-diethylthiosemicarbazone was studied. Experiments that used [3H]leucine for short-pulse labeling in the presence of the drug resulted in a 71% inhibition in the synthesis of Pr-80, the polypeptide precursor of the gag viral proteins. The radioactive pulse products of the polypeptide precursors after a further 2-h chase period showed a normal cleavage of the precursors, with the formation of a reduced amount of final mature viral structural proteins. The experimental evidence indicated that at the inhibitory concentration of 17 microM N-methylisatin-beta-4',4'-diethylthiosemicarbazone, the amount of intracellular viral RNA was not affected, whereas the activities of reverse transcriptase and the other viral protein syntheses were suppressed.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference19 articles.
1. Gag polyprotein precursors of Rauscher murine leukemia virus;Arcement L. J.;Virology,1977
2. Tumor viruses;Baltimore D.;Cold Spring Harbor Symp. Quant. Biol.,1974
3. Bauer D. J. 1972. In Thiosemicarbazone in chemotherapy of virus diseases vol. 1. Pergamon Press Oxford.
4. Assembly of type C oncornaviruses: a model;Bolognesi D. P.;Science,1978
5. New thiosemicarbazones of mono and bicyclic alpha-ketolactams;Edelstein F.;Eur. J. Med. Chem.,1980
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