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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  Separomics applied to the proteomics and peptidomics of low-abundance proteins: choice of methods and challenges - a review
Autores:  Baracat-Pereira,Maria Cristina
Barbosa,Meire de Oliveira
Magalhães Júnior,Marcos Jorge
Carrijo,Lanna Clicia
Games,Patrícia Dias
Almeida,Hebréia Oliveira
Sena Netto,José Fabiano
Pereira,Matheus Rodrigues
Barros,Everaldo Gonçalves de
Data:  2012-01-01
Ano:  2012
Palavras-chave:  Sample preparation
Complex protein extract
Subproteomes
Low-abundance proteins
Cell wall proteins
Resumo:  The enrichment and isolation of proteins are considered limiting steps in proteomic studies. Identification of proteins whose expression is transient, those that are of low-abundance, and of natural peptides not described in databases, is still a great challenge. Plant extracts are in general complex, and contaminants interfere with the identification of proteins involved in important physiological processes, such as plant defense against pathogens. This review discusses the challenges and strategies of separomics applied to the identification of low-abundance proteins and peptides in plants, especially in plants challenged by pathogens. Separomics is described as a group of methodological strategies for the separation of protein molecules for proteomics. Several tools have been used to remove highly abundant proteins from samples and also non-protein contaminants. The use of chromatographic techniques, the partition of the proteome into subproteomes, and an effort to isolate proteins in their native form have allowed the isolation and identification of rare proteins involved in different processes.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572012000200009
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/S1415-47572012000200009
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.35 n.1 suppl.1 2012
Direitos:  info:eu-repo/semantics/openAccess
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