Literature DB >> 6300437

Isolation and characterization of a membrane-bound population of group B coxsackieviruses.

N K Chatterjee, W A Samsonoff, C Tuchowski.   

Abstract

HeLa cells infected with several group B coxsackieviruses contain a previously undetected, virus-specific ribonucleoprotein particle which we designated membrane-bound virion (MBV). MBVs of B5 virus have a pronounced polygonal appearance and are slightly smaller than virions. The particles sediment more slowly (at about 107S) and have a lower buoyant density (about 1.30). They contain 35S virion RNA; only three, and not four, capsid proteins; and at least seven additional proteins with apparent molecular weights of 21,000 to 92,000. Three of the latter proteins appear to be of host origin; the rest may be precursors of virion capsid proteins. The RNA is resistant to digestion by RNase, and EDTA treatment disrupts the particle. MBVs are infectious, although significantly less so than virions. Cells infected with MBVs produce both types of progeny, virions and MBVs. In coinfected cultures, the yield of progeny is lower than in cells infected with virions alone, suggesting interference by MBVs. Synthesis of both types can be detected within 3.5 h after infection, and synthesis continues for 24 h.

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Year:  1983        PMID: 6300437      PMCID: PMC256477     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  26 in total

1.  The formation of poliovirus particles in association with the RNA replication complexes.

Authors:  L A Caliguiri; R W Compans
Journal:  J Gen Virol       Date:  1973-10       Impact factor: 3.891

2.  In vitro assembly of polioviruses. 3. Assembly of 14 S particles into empty capsids by poliovirus-infected HeLa cell membranes.

Authors:  M Perlin; B A Phillips
Journal:  Virology       Date:  1973-05       Impact factor: 3.616

3.  Defective interfering particles of poliovirus. I. Isolation and physical properties.

Authors:  C N Cole; D Smoler; E Wimmer; D Baltimore
Journal:  J Virol       Date:  1971-04       Impact factor: 5.103

4.  Characterization of poliovirus-specific structures associated with cytoplasmic membranes.

Authors:  L A Caliguiri; I Tamm
Journal:  Virology       Date:  1970-09       Impact factor: 3.616

5.  In vitro assembly of poliovirus-related particles.

Authors:  B A Phillips; D F Summers; J V Maizel
Journal:  Virology       Date:  1968-06       Impact factor: 3.616

6.  Heterogeneity of apparently empty poliovirus particles stained with phosphotungstic acid after heating of the virus at "low" temperature.

Authors:  N J Dimmock; W J Harris
Journal:  Virology       Date:  1967-04       Impact factor: 3.616

7.  Specific cleavage of viral proteins as steps in the synthesis and maturation of enteroviruses.

Authors:  J J Holland; E D Kiehn
Journal:  Proc Natl Acad Sci U S A       Date:  1968-07       Impact factor: 11.205

8.  A structural model for picornaviruses as suggested from an analysis of urea-degraded virions and procapsids of coxsackievirus B3.

Authors:  L Philipson; S T Beatrice; R L Crowell
Journal:  Virology       Date:  1973-07       Impact factor: 3.616

9.  Preparative two-dimensional polyacrylamide gel electrophoresis of 32 P-labeled RNA.

Authors:  R de Wachter; W Fiers
Journal:  Anal Biochem       Date:  1972-09       Impact factor: 3.365

10.  Defective viral particles and viral disease processes.

Authors:  A S Huang; D Baltimore
Journal:  Nature       Date:  1970-04-25       Impact factor: 49.962

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  3 in total

1.  Infectious hepatitis A virus particles produced in cell culture consist of three distinct types with different buoyant densities in CsCl.

Authors:  S M Lemon; R W Jansen; J E Newbold
Journal:  J Virol       Date:  1985-04       Impact factor: 5.103

2.  Membrane-bound virions of coxsackievirus B4: cellular localization, analysis of the genomic RNA, genome-linked protein, and effect on host macromolecular synthesis.

Authors:  N K Chatterjee; C Nejman
Journal:  Arch Virol       Date:  1985       Impact factor: 2.574

3.  Molecular cloning of the genome of a cardiotropic Coxsackie B3 virus: full-length reverse-transcribed recombinant cDNA generates infectious virus in mammalian cells.

Authors:  R Kandolf; P H Hofschneider
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

  3 in total

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