Abstract |
PTU-23, a selective inhibitor of the reproduction of encephalomyocarditis (EMC) virus in Krebs-II ascites carcinoma cells, counteracts the virus-induced shut-off of the host-cell protein synthesis reducing it from 32% to 19%. The compound does not inhibit the synthesis of virus-specific proteins; the electrophoretic profile in SDS- PAAG shows an increase in the peaks of some viral polypeptides, mainly A, E and epsilon. It is suggested that this effect is connected to the partial inhibition by PTU-23 of the synthesis of the viral 37S RNA, without affecting its translation activity and also to the inhibition of the synthesis of 20S (RF) RNA--an inhibitor of the virus-specific protein synthesis. PTU-23 does not affect the processing of the high-molecular-weight viral precursor polypeptide preA, which is carried out by the virus-specific protease protein p22, as shown in studies with a cell-free system.
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Authors | A S Galabov, V A Ginevskaya, Svitkin YuV |
Journal | Zentralblatt fur Bakteriologie, Mikrobiologie und Hygiene. 1. Abt. Originale A, Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie = International journal of microbiology and hygiene. A, Medical microbiology, infectious...
(Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol)
Vol. 254
Issue 3
Pg. 306-17
(May 1983)
ISSN: 0174-3031 [Print] Germany |
PMID | 6326422
(Publication Type: Journal Article)
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Chemical References |
- Antiviral Agents
- Neoplasm Proteins
- Viral Proteins
- N-phenyl-N'-3-hydroxyphenylthiourea
- Phenylthiourea
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Topics |
- Animals
- Antiviral Agents
(pharmacology)
- Carcinoma, Krebs 2
(metabolism, microbiology)
- Cells, Cultured
- Electrophoresis, Polyacrylamide Gel
- Encephalomyocarditis virus
(growth & development, metabolism)
- Mice
- Neoplasm Proteins
(biosynthesis)
- Phenylthiourea
(analogs & derivatives, pharmacology)
- Viral Proteins
(biosynthesis)
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