Abstract
After the attachment of radioactive coxsackievirus B3 to HeLa cells at 0 C and subsequent incubation at 37 C, 50 to 80% of attached virus radioactivity was eluted from the cells within 1 hr. Eluted virus had a buoyant density of 1.21 in a potassium tartrate gradient, sedimented more slowly than native virus in sucrose gradients, was resistant to ribonuclease, was unstable in CsCl centrifugation, and did not reattach to uninfected cells. Electrophoretic studies of sodium dodecyl sulfate-disrupted B3 virus in sodium dodecyl sulfate-polyacrylamide gels revealed four radioactive virus polypeptides (VP 1 to 4), of which the three largest migrated slightly faster than their poliovirus T1 counterparts. In contrast, electrophoretic analysis of eluted virus, after banding in a tartrate gradient or pelleting by centrifugation, showed the absence of the fastest migrating polypeptide, VP 4. VP 4 was recovered in the supernatant fluid when the eluted virions were removed by high-speed centrifugation. The results indicate that VP 4 is located at the surface of the native virion, and its dissociation from the capsid may represent the first specific alteration of the virion after virus-receptor interaction at the cell surface.
MeSH Terms
Amino Acids
Buffers
Carbon Isotopes
Centrifugation, Density Gradient
Cesium
Chlorides
Electrophoresis, Disc
Enterovirus/analysis,isolation & purification,pathogenicity
HeLa Cells
Humans
Molecular Weight
Peptides/analysis
Phosphates
Phosphorus Isotopes
Poliovirus/analysis,isolation & purification
Potassium
Ribonucleases
Sucrose
Tartrates
Temperature
Tritium
Valine
Viral Proteins/analysis
Virus Replication
Chemicals
Amino Acids
Buffers
Carbon Isotopes
Chlorides
Peptides
Phosphates
Phosphorus Isotopes
Tartrates
Viral Proteins
Tritium
Cesium
Sucrose
Ribonucleases
Valine
Potassium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Crowell R L
Philipson L
References (15)
15 references, click to expand
-
Evidence for ambiguity in the posttranslational cleavage of poliovirus proteins.
Virology. 1970 Jul;41(3):408-18
PMID: 4316554
-
Replication of poliovirus RNA studied by gel filtration and electrophoresis.
Eur J Biochem. 1969 Dec;11(2):305-15
PMID: 4311781
-
Differential inhibition of attachment and eclipse activities of HeLa cells for enteroviruses.
J Virol. 1969 Apr;3(4):422-8
PMID: 4306196
-
The adsorption and early fate of purified poliovirus in HeLa cells.
Virology. 1961 Apr;13:439-47
PMID: 13790415
-
The early interaction of coxsackievirus B3 with HeLa cells.
Proc Soc Exp Biol Med. 1971 Jul;137(3):1082-8
PMID: 5560655
-
The structure of heated poliovirus particles.
J Gen Virol. 1971 Jun;11(3):147-56
PMID: 4105288
-
Amino acid metabolism in mammalian cell cultures.
Science. 1959 Aug 21;130(3373):432-7
PMID: 13675766
-
Specific cleavage of viral proteins as steps in the synthesis and maturation of enteroviruses.
Proc Natl Acad Sci U S A. 1968 Jul;60(3):1015-22
PMID: 4299264
-
The mammalian cell-virus relationship. VI. Sustained infection of HeLa cells by Coxsackie B3 virus and effect on superinfection.
J Exp Med. 1961 Feb 1;113:419-35
PMID: 13696665
-
Specific cell-surface alteration by enteroviruses as reflected by viral-attachment interference.
J Bacteriol. 1966 Jan;91(1):198-204
PMID: 4285531
-
Evidence for differences in size and composition of the poliovirus-specific polypeptides in infected HeLa cells.
Virology. 1968 Sep;36(1):48-54
PMID: 4299390
-
Plaque formation and isolation of pure lines with poliomyelitis viruses.
J Exp Med. 1954 Feb;99(2):167-82
PMID: 13130792
-
The inhibition of poliovirus growth by actinomycin D and the prevention of the inhibition by pretreatment of the cells with serum or insulin.
Virology. 1966 Apr;28(4):663-78
PMID: 4287204
-
Acrylamide-gel electrophorograms by mechanical fractionation: radioactive adenovirus proteins.
Science. 1966 Feb 25;151(3713):988-90
PMID: 5907290
-
Early interactions between poliovirus and ERK cells: some observations on the nature and significance of the rejected particles.
Virology. 1962 Oct;18:212-23
PMID: 13962933