Your browser doesn't support javascript.
loading
Fluorescence resonance energy transfer analysis for detecting protein kinase C activation / 南方医科大学学报
Journal of Southern Medical University ; (12): 1867-1870, 2011.
Artigo em Chinês | WPRIM | ID: wpr-333794
ABSTRACT
<p><b>OBJECTIVE</b>To establish a sensitive and direct method for detecting the activation of protein kinase C (PKC) using fluorescence resonance energy transfer (FRET) technique.</p><p><b>METHODS</b>HEK293 cells were transfected with C kinase activity reporter (CKAR) plasmid or/and parathyroid receptor 1 plasmid , and after incubation for 72 h, the fluorescence resonance energy transfer was measured with or without parathyroid or TPA stimulation.</p><p><b>RESULTS</b>TPA reduced the efficiency of FRET and increased the emission ratio of CFP/YFP (C/Y) in HEK293 cells transfected with CKAR. PTH(1-34) could increase the emission ratio of C/Y in HEK293 cells co-transfected with CKAR and PTHR1 but not in cells transfected with CKAR.</p><p><b>CONCLUSION</b>FRET analysis using CKAR can be utilized to detect the activation of PKC, which provides a useful means for studying the signaling pathways associated with PKC.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteínas de Bactérias / Proteína Quinase C / Química / Genes Reporter / Transferência Ressonante de Energia de Fluorescência / Ativação Enzimática / Células HEK293 / Proteínas Luminescentes / Metabolismo / Métodos Limite: Humanos Idioma: Chinês Revista: Journal of Southern Medical University Ano de publicação: 2011 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteínas de Bactérias / Proteína Quinase C / Química / Genes Reporter / Transferência Ressonante de Energia de Fluorescência / Ativação Enzimática / Células HEK293 / Proteínas Luminescentes / Metabolismo / Métodos Limite: Humanos Idioma: Chinês Revista: Journal of Southern Medical University Ano de publicação: 2011 Tipo de documento: Artigo