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PubMed · 4359418

Sendai virion transcriptase complex: polyeptide composition and inhibition by virion envelope proteins.

P A Marx·A Portner·D W Kingsbury
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Abstract

Sendai virions, disrupted in 2% Triton X-100 in 1 M KCl, were separated into nucleocapsids and envelope proteins by centrifugation. The nucleocapsids, representing 46% of the virion proteins, had a buoyant density of 1.29 gm/cm(3) in D(2)O sucrose. RNA-dependent transcriptase activity associated with them had a ninefold greater specific activity than transcriptase assayed in unfractionated detergent-disrupted virions. These enzyme-active nucleocapsids contained only two polypeptides, the largest virion polypeptide (molecular weight 75,000) and the nucleocapsid structure unit (molecular weight 60,000). Virion envelope proteins, either glycoproteins or nonglycosylated matrix protein, inhibited nucleocapsid-associated polymerase activity; brief heat denaturation abolished their inhibitory activity. Yeast RNA stimulated nucleocapsid-associated enzyme, suggesting that stimulatory polyanions act at the enzyme-template level.

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Cell-Free SystemCentrifugation, Density GradientDNA-Directed RNA PolymerasesElectrophoresis, Polyacrylamide GelGlycopeptidesGuanosine TriphosphateNucleoproteinsParainfluenza Virus 1, HumanPeptidesRNASurface-Active AgentsTritiumViral ProteinsYeastsJournal Article

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P A Marx, A Portner, D W Kingsbury. 1974. Sendai virion transcriptase complex: polyeptide composition and inhibition by virion envelope proteins.. https://doi.org/10.1128/jvi.13.1.107-112.1974

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