scispace - formally typeset
Open AccessJournal ArticleDOI

Proteins of vesicular stomatitis virus: kinetics and cellular sites of synthesis.

Robert R. Wagner, +2 more
- 01 May 1970 - 
- Vol. 5, Iss: 5, pp 548-558
TLDR
These experiments are compatible with the hypothesis that VS viral proteins G and S are synthesized at and inserted into plasma membrane which envelopes a nucleocapsid core to form the VS virion.
Abstract
FIVE VIRAL PEPTIDES SYNTHESIZED IN L CELLS INFECTED WITH VESICULAR STOMATITIS (VS) VIRUS WERE IDENTIFIED BY POLYACRYLAMIDE GEL ELECTROPHORESIS AND DESIGNATED AS FOLLOWS: nucleoprotein N, a membrane glycoprotein G, a membrane surface protein S, and two nonstructural proteins NS1 and NS2. A slowly migrating minor structural protein L also present in infected cells is probably an aggregate. Incorporation of (3)H-amino acids into each viral protein could be detected by the 2nd hr after infection and even earlier for protein N which is synthesized in the greatest amount. There was no evidence of regulation of viral protein synthesis at the transcriptive level; nonstructural and structural proteins were synthesized throughout the cycle of infection. Short pulses of (3)H-amino acids revealed no uncleaved precursor peptides that could be chased into structural peptides. Proteins N and S were chased into released virions but protein G was apparently incorporated into virions as it was being synthesized. VS viral proteins of infected cells were released by mechanically disrupting cytoplasmic membrane by nitrogen decompression and fractionated by high-speed centrifugation. Protein NS1 was present in the nonsedimentable cytoplasmic fraction throughout the cycle of infection. The nucleoprotein N was recovered primarily from the nonsedimentable fraction early in infection but aggregated into a sedimentable component, presumably the nucleocapsid, later in infection. Proteins G and S were always present in the sedimentable fraction of mechanically disrupted infected cells, presumably in association with plasma membrane. Exposure of infected cells to the membrane-dissolving agent, digitonin, resulted in solubilization of most of protein G and all of protein S but not of protein N. These experiments are compatible with the hypothesis that VS viral proteins G and S are synthesized at and inserted into plasma membrane which envelopes a nucleocapsid core to form the VS virion.

read more

Citations
More filters
Journal ArticleDOI

Both NS and L proteins are required for in vitro RNA synthesis by vesicular stomatitis virus.

S U Emerson, +1 more
- 01 Jun 1975 - 
TL;DR: Results of the polymerase assays indicate that both L and NS proteins are required to reconstitute transcription activity with a highly purified template composed of only RNA and N protein.
Journal ArticleDOI

Tunicamycin inhibits glycosylation and multiplication of Sindbis and vesicular stomatitis viruses.

TL;DR: It is demonstrated that TM specifically inhibits the glycosylation of viral glycoproteins and that gly cosylation may be essential for the normal assembly of enveloped viral particles.
Book ChapterDOI

Reproduction of Rhabdoviruses

TL;DR: The rhabdoviruses are ubiquitous, highly infectious agents of animal and plant disease and are generally transmitted by arthropods and are, therefore, susceptible to disruption by ether and detergents.
Journal ArticleDOI

The glycoprotein of vesicular stomatitis virus is the antigen that gives rise to and reacts with neutralizing antibody

TL;DR: The glycoprotein, but no other virion protein, of vesicular stomatitis virus was solubilized by the nonionic detergent Triton X-100 in low ionic strength buffer and induced the synthesis of antibody that formed a single precipitin line with the glycop protein and neutralized the infectivity of the virus.
References
More filters
Journal ArticleDOI

The submitochondrial localization of monoamine oxidase. An enzymatic marker for the outer membrane of rat liver mitochondria.

TL;DR: Digitonin treatment released more monoamine oxidase than cytochrome oxidase from sonic particles, thus indicating that digitonin preferentially degrades the outer mitochondrial membrane.
Journal ArticleDOI

Acrylamide-gel electrophorograms by mechanical fractionation: radioactive adenovirus proteins.

TL;DR: An electrophorogram of radioactive type-2 adenovirus proteins so fractionated gave a pattern in excellent agreement with the pattern obtained by laborious manual sectioning and in agreement withThe pattern obtained on a replicate gel stained with Coomassie brilliant blue R250.
Journal ArticleDOI

Polypeptide cleavages in the formation of poliovirus proteins

TL;DR: It is found that cleavages play an important role in the formation of most if not all poliovirus-specific proteins.
Journal ArticleDOI

Evidence for large precursor proteins in poliovirus synthesis.

TL;DR: Experiments with brief C14-amino acid pulses, followed by chases of varying duration, indicate that only some of the polypeptides seen in acrylamide gel electropherograms are "primary" translation products of the virus mRNA, and that others are "secondary" products which arise by conversion fromsome of the " primary" proteins.
Related Papers (5)