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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Human respiratory syncytial virus N, P and M protein interactions in HEK-293T cells

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Author(s):
Oliveira, Andressa P. [1] ; Simabuco, Fernando M. [1, 2] ; Tamura, Rodrigo E. [1, 3] ; Guerrero, Manuel C. [4] ; Ribeiro, Paulo G. G. [1] ; Libermann, Towia A. [4] ; Zerbini, Luiz F. [4, 5, 6] ; Ventura, Armando M. [1]
Total Authors: 8
Affiliation:
[1] Univ Sao Paulo, Dept Microbiol, Inst Ciencias Biomed, BR-05508900 Sao Paulo - Brazil
[2] Univ Estadual Campinas, Fac Ciencias Aplicadas, Sao Paulo - Brazil
[3] Inst Canc Estado Sao Paulo Octavio Frias de Olive, Ctr Invest Translac Oncol CTO, Sao Paulo - Brazil
[4] Harvard Univ, Sch Med, BIDMC Genom Ctr, Boston, MA - USA
[5] Univ Cape Town, ICGEB, ZA-7925 Cape Town - South Africa
[6] Univ Cape Town, Div Med Biochem, ZA-7925 Cape Town - South Africa
Total Affiliations: 6
Document type: Journal article
Source: VIRUS RESEARCH; v. 177, n. 1, p. 108-112, OCT 2013.
Web of Science Citations: 17
Abstract

Characterization of Human Respiratory Syncytial Virus (HRSV) protein interactions with host cell components is crucial to devise antiviral strategies. Viral nucleoprotein, phosphoprotein and matrix protein genes were optimized for human codon usage and cloned into expression vectors. HEK-293T cells were transfected with these vectors, viral proteins were immunoprecipitated, and co-immunoprecipitated cellular proteins were identified through mass spectrometry. Cell proteins identified with higher confidence scores were probed in the immunoprecipitation using specific antibodies. The results indicate that nucleoprotein interacts with arginine methyl-transferase, methylosome protein and Hsp70. Phosphoprotein interacts with Hsp70 and tropomysin, and matrix with tropomysin and nucleophosmin. Additionally, we performed immunoprecipitation of these cellular proteins in cells infected with HRSV, followed by detection of co-immunoprecipitated viral proteins. The results indicate that these interactions also occur in the context of viral infection, and their potential contribution for a HRSV replication model is discussed. (C) 2013 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 09/17587-9 - Human Respiratory Syncytial Virus immunization and molecular studies
Grantee:Armando Morais Ventura
Support Opportunities: Regular Research Grants