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Direct evidence of cytoplasmic delivery of PKC-alpha, -epsilon and -zeta pseudosubstrate lipopeptides: study of their implication in the induction of apoptosis.
Thiam, K; Loing, E; Zoukhri, D; Rommens, C; Hodges, R; Dartt, D; Verwaerde, C; Auriault, C; Gras-Masse, H; Sergheraert, C.
Afiliação
  • Thiam K; UMR 8727, Lille II University, Institut de Biologie et Institut Pasteur de Lille, 1 rue du Pr. A. Calmette, P.O. Box 447, 59021, Lille, France. kader.thiam@pasteur-lille.fr
FEBS Lett ; 459(3): 285-90, 1999 Oct 15.
Article em En | MEDLINE | ID: mdl-10526151
ABSTRACT
Protein kinases C (PKC) are serine/threonine kinase enzymes involved in the mechanism of cell survival. Their pseudosubstrate sequences are autoinhibitory domains, which maintain the enzyme in an inactive state in the absence of allosteric activators, thus representing an attractive tool for the modulation of different PKC isoforms. Here, we report the use of palmitoylated modified PKC-alpha, -epsilon, and -zeta pseudosubstrate peptides, and determine their intracellular distribution together with their respective PKC isoenzymes. Finally, we propose that the differential distribution of the peptides is correlated with a selective induction of apoptosis and therefore argues for different involvement of PKC isoforms in the anti-apoptotic program.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteína Quinase C / Apoptose / Isoenzimas Limite: Humans Idioma: En Revista: FEBS Lett Ano de publicação: 1999 Tipo de documento: Article País de afiliação: França
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteína Quinase C / Apoptose / Isoenzimas Limite: Humans Idioma: En Revista: FEBS Lett Ano de publicação: 1999 Tipo de documento: Article País de afiliação: França