Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Forensic Proteomics of Poxvirus Production

Journal Article · · Analyst, 138(21):6385-6397
DOI:https://doi.org/10.1039/c3an00711a· OSTI ID:1132723
The field of microbial forensics has recently sought to develop methods to discern biological signatures to indicate production methods for biological agents. Viral agents have received less attention to date. Their obligate propagation in living cells makes purification from cellular material a challenge. This leads to potential carryover of protein-rich signature of their production system. Here we have explored a proteomic analysis of Vaccinia virus as a model poxvirus system in which to compare samples of virus propagated in different cell lines and subjected to different purification schemes. The proteomic data sets indicated viral, host cell and culture medium proteins, and several layers of data analysis were applied to build confidence in the peptide identification and capture information on the taxonomic utility of each. The analysis showed clear shifts in protein profiles with virus purification, with successive gradient purification steps showing different levels of viral protein enrichment. Peptides from cellular proteins, including those present in purified virus preparations, provided signatures which enabled discrimination of cell line substrates, including distinguishing between cells derived from different primate species. The ability to discern multiple aspects of viral production demonstrates the potential value of proteomic analysis as tool for microbial forensics.
Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
1132723
Report Number(s):
PNNL-SA-93087; 400904120
Journal Information:
Analyst, 138(21):6385-6397, Journal Name: Analyst, 138(21):6385-6397
Country of Publication:
United States
Language:
English

Similar Records

Structure-Function Analysis of Vaccinia Virus H7 Protein Reveals a Novel Phosphoinositide Binding Fold Essential for Poxvirus Replication
Journal Article · Tue Dec 02 23:00:00 EST 2014 · Journal of Virology · OSTI ID:1208677

The Structure of the Poxvirus A33 Protein Reveals a Dimer of Unique C-Type Lectin-Like Domains
Journal Article · Wed Nov 03 00:00:00 EDT 2010 · J. Virol. · OSTI ID:1002283

Structure of the poxvirus decapping enzyme D9 reveals its mechanism of cap recognition and catalysis
Journal Article · Mon Mar 14 00:00:00 EDT 2022 · Structure · OSTI ID:1981769

Related Subjects