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Coexpression of PXRLBD with SRC88 and construction of equilibrium dialysis model of screening PXR ligands / 药学学报
Acta Pharmaceutica Sinica ; (12): 427-430, 2008.
Artículo en Chino | WPRIM | ID: wpr-277836
ABSTRACT
The aim of this study was to obtain the soluble protein of human pregnane X receptor ligand binding domain (PXRLBD) through the coexpression of PXRLBD and 88 amino acids of steroid receptor coactivator-1 (SRC88) and apply the protein to constructing a new model of screening PXR ligands. Expression plasmid of pETDuet-1-SRC88-PXRLBD was constructed and transformed into Escherichia coli Rosetta (DE3) to coexpress PXRLBD and SRC88 via induction by IPTG at low temperature. Then an equilibrium dialysis model was constructed to study the interaction between PXRLBD and drugs including clotrimazole and dexamethasone, using HPLC as the analysis method. The results showed that the soluble protein of PXRLBD was obtained and the HPLC data indicated that clotrimazole bound to PXRLBD, while dexamethasone did not bind to PXRLBD, which indicated the successful establishment of a new method for studying the interaction between PXR and drugs. The new method may be useful in the screening of PXR ligands in vitro.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Plásmidos / Unión Proteica / Factores de Transcripción / Transformación Genética / Dexametasona / Receptores de Esteroides / Clotrimazol / Diálisis / Interacciones Farmacológicas / Escherichia coli Tipo de estudio: Estudio diagnóstico / Estudio pronóstico / Estudio de tamizaje Límite: Humanos Idioma: Chino Revista: Acta Pharmaceutica Sinica Año: 2008 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Plásmidos / Unión Proteica / Factores de Transcripción / Transformación Genética / Dexametasona / Receptores de Esteroides / Clotrimazol / Diálisis / Interacciones Farmacológicas / Escherichia coli Tipo de estudio: Estudio diagnóstico / Estudio pronóstico / Estudio de tamizaje Límite: Humanos Idioma: Chino Revista: Acta Pharmaceutica Sinica Año: 2008 Tipo del documento: Artículo