Rabies virus protein synthesis in infected BHK-21 cells
نویسندگان
چکیده
منابع مشابه
Rabies virus protein synthesis in infected BHK-21 cells.
Rabies virus specific polypeptide synthesis was examined under hypertonic conditions, which selectively inhibit cellular protein synthesis. The rabies virus proteins (L, G, N, M1, M2) were synthesized throughout the course of infection, with little change in their relative rates of synthesis. The rates of synthesis of the G and M1 polypeptides were more sensitive to increasing osmolarity than t...
متن کاملSelective suppression of cellular protein synthesis in BHK-21 cells infected with rabies virus.
Under hypertonic conditions, cellular protein synthesis is selectively suppressed in rabies virus-infected cells. The resistance of viral polypeptide synthesis to hypertonic conditions provides a means to study intracellular viral protein synthesis and may represent a property common to translation of many viruses.
متن کاملLipids of rabies virus and BHK-21 cell membranes.
The lipid composition of highly purified Flury strain of rabies virus (HEP) propagated in BHK-21 cells in a chemically defined medium was observed to be 6.7% neutral lipids, 15.8% phospholipids, and 1.5% glycolipids. In the virion, phosphatidylethanolamine, phosphatidylcholine, and sphingomyelin were the most abundant phospholipids, accounting for 90% of the total, and the molar ratio of choles...
متن کاملBeta-propiolactone treatment impairs the biological activity of residual DNA from BHK-21 cells infected with rabies virus.
The effects of beta-propiolactone (BPL), an alkylating and virus inactivating agent, on the structural and in vitro biological properties of different DNA preparations from BHK-21 cells were investigated. Both uninfected and rabies virus-infected cells were used. Purified cellular DNA (celDNA) was used as the reference, and supernatants from infected cells were treated with BPL. For structural ...
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ژورنال
عنوان ژورنال: Journal of Virology
سال: 1977
ISSN: 0022-538X,1098-5514
DOI: 10.1128/jvi.22.1.102-112.1977