Please use this identifier to cite or link to this item: https://doi.org/10.1074/mcp.M500149-MCP200
Title: Proteomic studies of the Singapore grouper iridovirus
Authors: Song, W.
Lin, Q. 
Joshi, S.B. 
Lim, T.K. 
Hew, C.-L. 
Issue Date: Feb-2006
Citation: Song, W., Lin, Q., Joshi, S.B., Lim, T.K., Hew, C.-L. (2006-02). Proteomic studies of the Singapore grouper iridovirus. Molecular and Cellular Proteomics 5 (2) : 256-264. ScholarBank@NUS Repository. https://doi.org/10.1074/mcp.M500149-MCP200
Abstract: The Singapore grouper iridovirus (SGIV) genome consists of a double-stranded circular DNA of 140,131 base pairs with 162 predicted open reading frames. Our earlier study using peptide mass fingerprints generated from MALDITOF MS led to the identification of 26 viral proteins. The present investigation aimed to achieve a more comprehensive and precise identification of the SGIV viral proteome by two workflows: one-dimensional gel electrophoresis (I-DE) separation followed by protein identification by MALDI-TOF/TOF MS/MS (1-DE-MALDI workflow) and shotgun proteornics in which the whole virus was digested by trypsin and the resulting peptides were separated by nano-LC and analyzed by MALDI-TOF/TOF MS/MS (LC-MALDI workflow). In total, 44 viral proteins were identified, 25 of which were reported for the first time. Fourteen proteins were uniquely identified by the 1-DE-MALDI workflow, whereas another 10 proteins were only identified by the LC-MALDI workflow with 20 proteins found by both approaches. Moreover 13 proteins were found to have acetylated N termini. Twenty-three proteins identified contain predicted transmembrane domains, accounting for 52.3% of the total proteins identified. RT-PCR confirmed the transcription products of all the identified viral proteins. A large number of proteins identified by both the 1-DE-MALDI and the LC-MALDI workflows from this study have significantly enhanced the coverage of the SGIV proteome. The SGIV proteome is at present the only iridoviral proteome that has been extensively characterized. Our results should provide further insights into the biology of SGIV and other iridoviruses. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.
Source Title: Molecular and Cellular Proteomics
URI: http://scholarbank.nus.edu.sg/handle/10635/101488
ISSN: 15359476
DOI: 10.1074/mcp.M500149-MCP200
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