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Further characterization of an adenosine-containing modification of vaccinia virus proteins
Abstract:
Three vaccinia virus (VV) core proteins which become labeled when virus is grown in the presence of radiolabeled adenosine or orthophosphate were identified as the major viral core proteins 4A, 4B, and 25K on the basis of comigration with [35S]methionine-labeled viral proteins and immunoprecipitation with monospecific polyclonal antisera. Boronate affinity chromatography and HPLC analysis suggested that a cis-diol-containing adenosine compound is present on this set of viral proteins. The replication of VV in tissue culture cells was prevented by the ADP-ribosylation inhibitors nicotinamide (NIC), 3-aminobenzamide (3-AB), and meta-iodobenzylguanidine (MIBG). None of these compounds significantly affected viral DNA synthesis at lower drug concentrations, although at higher concentrations of the three drugs a reduction in viral DNA synthesis was evident. Total VV protein synthesis also decreased at higher inhibitor levels, and the proteolytic processing of the major virion core proteins was greatly diminished as well. The three inhibitors also affected labeling of viral core proteins and cellular histone proteins by [8-14C]adenosine. In addition, mature, infectious virus particles were not formed in the presence of either 60 mM NIC or 3-AB, or 0.6 mM MIBG. These results provide evidence that the major VV core proteins are subject to modification by an adenosine compound, and suggest the possibility that this modification might represent ADP-ribosylation.
Insights
Three vaccinia virus core proteins are modified by an adenosine compound, potentially through ADP-ribosylation. This modification is crucial for viral replication and infectious virus particle formation.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Vaccinia virus (VV) is a large DNA virus with a complex structure.
- Core proteins are essential for viral function and replication.
Purpose of the Study:
- To identify and characterize modifications on vaccinia virus core proteins.
- To investigate the role of these modifications in viral replication.
Main Methods:
- Radiolabeling of vaccinia virus with adenosine or orthophosphate.
- Protein identification using comigration and immunoprecipitation.
- Analysis of adenosine compound modification using boronate affinity chromatography and HPLC.
- Inhibition of viral replication using ADP-ribosylation inhibitors (nicotinamide, 3-aminobenzamide, meta-iodobenzylguanidine).
Main Results:
- Identified major VV core proteins 4A, 4B, and 25K as being modified by an adenosine compound.
- ADP-ribosylation inhibitors blocked VV replication and formation of infectious virus particles.
- Inhibitors also reduced viral DNA and protein synthesis, and proteolytic processing of core proteins.
- Inhibitors affected labeling of viral core and cellular histone proteins by adenosine.
Conclusions:
- Major VV core proteins are modified by an adenosine compound, likely via ADP-ribosylation.
- This modification is essential for VV replication and the production of infectious virions.