Literature DB >> 20530633

Protein analysis of purified respiratory syncytial virus particles reveals an important role for heat shock protein 90 in virus particle assembly.

Anuradha Radhakrishnan1, Dawn Yeo, Gaie Brown, Myint Zu Myaing, Laxmi Ravi Iyer, Roland Fleck, Boon-Huan Tan, Jim Aitken, Duangmanee Sanmun, Kai Tang, Andy Yarwood, Jacob Brink, Richard J Sugrue.   

Abstract

In this study, we used imaging and proteomics to identify the presence of virus-associated cellular proteins that may play a role in respiratory syncytial virus (RSV) maturation. Fluorescence microscopy of virus-infected cells revealed the presence of virus-induced cytoplasmic inclusion bodies and mature virus particles, the latter appearing as virus filaments. In situ electron tomography suggested that the virus filaments were complex structures that were able to package multiple copies of the virus genome. The virus particles were purified, and the protein content was analyzed by one-dimensional nano-LC MS/MS. In addition to all the major virus structural proteins, 25 cellular proteins were also detected, including proteins associated with the cortical actin network, energy pathways, and heat shock proteins (HSP70, HSC70, and HSP90). Representative actin-associated proteins, HSC70, and HSP90 were selected for further biological validation. The presence of beta-actin, filamin-1, cofilin-1, HSC70, and HSP90 in the virus preparation was confirmed by immunoblotting using relevant antibodies. Immunofluorescence microscopy of infected cells stained with antibodies against relevant virus and cellular proteins confirmed the presence of these cellular proteins in the virus filaments and inclusion bodies. The relevance of HSP90 to virus infection was examined using the specific inhibitors 17-N-Allylamino-17-demethoxygeldanamycin. Although virus protein expression was largely unaffected by these drugs, we noted that the formation of virus particles was inhibited, and virus transmission was impaired, suggesting an important role for HSP90 in virus maturation. This study highlights the utility of proteomics in facilitating both our understanding of the role that cellular proteins play during RSV maturation and, by extrapolation, the identification of new potential targets for antiviral therapy.

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Year:  2010        PMID: 20530633      PMCID: PMC2938102          DOI: 10.1074/mcp.M110.001651

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  98 in total

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Review 3.  Recruitment of Hsp70 chaperones: a crucial part of viral survival strategies.

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4.  Cooperativity of actin and microtubule elements during replication of respiratory syncytial virus.

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5.  Antiviral activity and RNA polymerase degradation following Hsp90 inhibition in a range of negative strand viruses.

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Review 6.  Development and application of Hsp90 inhibitors.

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Review 9.  Role of multivesicular bodies and their components in the egress of enveloped RNA viruses.

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Review 4.  Proteomics Tracing the Footsteps of Infectious Disease.

Authors:  Todd M Greco; Ileana M Cristea
Journal:  Mol Cell Proteomics       Date:  2017-02-05       Impact factor: 5.911

Review 5.  Respiratory Syncytial Virus: Infection, Detection, and New Options for Prevention and Treatment.

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Journal:  Mol Cell Proteomics       Date:  2015-01-02       Impact factor: 5.911

Review 7.  Molecular mechanisms driving respiratory syncytial virus assembly.

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Journal:  Future Microbiol       Date:  2013-01       Impact factor: 3.165

8.  The Impact of Mass Spectrometry-Based Proteomics on Fundamental Discoveries in Virology.

Authors:  Todd M Greco; Benjamin A Diner; Ileana M Cristea
Journal:  Annu Rev Virol       Date:  2014-07-14       Impact factor: 10.431

9.  The Respiratory Syncytial Virus Phosphoprotein, Matrix Protein, and Fusion Protein Carboxy-Terminal Domain Drive Efficient Filamentous Virus-Like Particle Formation.

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