Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.

Baculovirus infection of Spodoptera frugiperda cells is a system of choice to produce a range of recombinant proteins, vaccines and, potentially, gene therapy vectors. While baculovirus genomes are well characterized, the genome of S. frugiperda is not sequenced and the virus-host molecular interpla...

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Main Authors: Nuno Carinhas, Aaron Mark Robitaille, Suzette Moes, Manuel José Teixeira Carrondo, Paul Jenoe, Rui Oliveira, Paula Marques Alves
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3196586?pdf=render
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spelling doaj-177ad084a98c4563a6c3cad10b7b526c2020-11-25T02:04:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2644410.1371/journal.pone.0026444Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.Nuno CarinhasAaron Mark RobitailleSuzette MoesManuel José Teixeira CarrondoPaul JenoeRui OliveiraPaula Marques AlvesBaculovirus infection of Spodoptera frugiperda cells is a system of choice to produce a range of recombinant proteins, vaccines and, potentially, gene therapy vectors. While baculovirus genomes are well characterized, the genome of S. frugiperda is not sequenced and the virus-host molecular interplay is sparsely known. Herein, we describe the application of stable isotope labeling by amino acids in cell culture (SILAC) to obtain the first comparative proteome quantitation of S. frugiperda cells during growth and early baculovirus infection. The proteome coverage was maximized by compiling a search database with protein annotations from insect species. Of interest were differentially proteins related to energy metabolism, endoplasmic reticulum and oxidative stress, yet not investigated in the scope of baculovirus infection. Further, the reduced expression of key viral-encoded proteins early in the infection cycle is suggested to be related with decreased viral replication at high cell density culture. These findings have implications for virological research and improvement of baculovirus-based bioprocesses.http://europepmc.org/articles/PMC3196586?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nuno Carinhas
Aaron Mark Robitaille
Suzette Moes
Manuel José Teixeira Carrondo
Paul Jenoe
Rui Oliveira
Paula Marques Alves
spellingShingle Nuno Carinhas
Aaron Mark Robitaille
Suzette Moes
Manuel José Teixeira Carrondo
Paul Jenoe
Rui Oliveira
Paula Marques Alves
Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
PLoS ONE
author_facet Nuno Carinhas
Aaron Mark Robitaille
Suzette Moes
Manuel José Teixeira Carrondo
Paul Jenoe
Rui Oliveira
Paula Marques Alves
author_sort Nuno Carinhas
title Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
title_short Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
title_full Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
title_fullStr Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
title_full_unstemmed Quantitative proteomics of Spodoptera frugiperda cells during growth and baculovirus infection.
title_sort quantitative proteomics of spodoptera frugiperda cells during growth and baculovirus infection.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Baculovirus infection of Spodoptera frugiperda cells is a system of choice to produce a range of recombinant proteins, vaccines and, potentially, gene therapy vectors. While baculovirus genomes are well characterized, the genome of S. frugiperda is not sequenced and the virus-host molecular interplay is sparsely known. Herein, we describe the application of stable isotope labeling by amino acids in cell culture (SILAC) to obtain the first comparative proteome quantitation of S. frugiperda cells during growth and early baculovirus infection. The proteome coverage was maximized by compiling a search database with protein annotations from insect species. Of interest were differentially proteins related to energy metabolism, endoplasmic reticulum and oxidative stress, yet not investigated in the scope of baculovirus infection. Further, the reduced expression of key viral-encoded proteins early in the infection cycle is suggested to be related with decreased viral replication at high cell density culture. These findings have implications for virological research and improvement of baculovirus-based bioprocesses.
url http://europepmc.org/articles/PMC3196586?pdf=render
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