Weekes, Michael P., Tomasec, Peter, Huttlin, Edward L., Fielding, Ceri A. ORCID: https://orcid.org/0000-0002-5817-3153, Nusinow, David, Stanton, Richard J. ORCID: https://orcid.org/0000-0002-6799-1182, Wang, Eddie C. Y. ORCID: https://orcid.org/0000-0002-2243-4964, Aicheler, Rebecca, Murrell, Isa, Wilkinson, Gavin W. G. ORCID: https://orcid.org/0000-0002-5623-0126, Lehner, Paul J. and Gygi, Steven P. 2014. Quantitative temporal viromics: an approach to investigate host-pathogen interaction. Cell 157 (6) , pp. 1460-1472. 10.1016/j.cell.2014.04.028 |
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Abstract
A systematic quantitative analysis of temporal changes in host and viral proteins throughout the course of a productive infection could provide dynamic insights into virus-host interaction. We developed a proteomic technique called “quantitative temporal viromics” (QTV), which employs multiplexed tandem-mass-tag-based mass spectrometry. Human cytomegalovirus (HCMV) is not only an important pathogen but a paradigm of viral immune evasion. QTV detailed how HCMV orchestrates the expression of >8,000 cellular proteins, including 1,200 cell-surface proteins to manipulate signaling pathways and counterintrinsic, innate, and adaptive immune defenses. QTV predicted natural killer and T cell ligands, as well as 29 viral proteins present at the cell surface, potential therapeutic targets. Temporal profiles of >80% of HCMV canonical genes and 14 noncanonical HCMV open reading frames were defined. QTV is a powerful method that can yield important insights into viral infection and is applicable to any virus with a robust in vitro model.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine Systems Immunity Research Institute (SIURI) |
Subjects: | R Medicine > R Medicine (General) |
Publisher: | Elsevier |
ISSN: | 0092-8674 |
Funders: | Wellcome Trust, MRC |
Date of First Compliant Deposit: | 18 January 2021 |
Date of Acceptance: | 3 April 2014 |
Last Modified: | 13 Feb 2024 12:53 |
URI: | https://orca.cardiff.ac.uk/id/eprint/67609 |
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