国家自然科学基金重点项目资助(39830400).
This work was supported by a grant from Key Program of National Natural Science Foundation of China(39830400).
建立p38丝裂原活化蛋白激酶(mitogen-activated protein kinase, MAPK)放射自显影激酶活性测定方法,并应用于血管内皮细胞中p38 MAPK活性动态变化的研究.结果表明放射自显影激酶活性测定方法具有很好的量效关系、灵敏性和特异性.在脂多糖(lipopolysaccharide, LPS)刺激的血管内皮细胞,p38 MAPK在LPS刺激15 min后活性增高,30~60 min达高峰,120 min后活性逐渐下降,较好地反映了LPS刺激的内皮细胞中p38 MAPK活性的动态变化.国内实验室完全有可能和条件,建立本国的放射自显影激酶活性测定方法,并应用于信号转导的研究.
Autoradiograph assay of p38 MAPK (mitogen-activated protein kinase) activity was established, and applied in measurement of p38 MAPK activity of vascular endothelial cell stimulated by lipopolysaccharide (LPS). Results showed that autoradiograph assay possessed specificity and sensitivity. Activity of p38 MAPK in endothelial cell treated by LPS was increased at 15 min, and reached maximum value during 30~60 min,then descended. It suggested that domestic laboratory completely had the ability to establish autoradiograph assay of kinase activity,and applied in study of signal transduction.
闫文生,姜勇,黄巧冰,赵克森. p38丝裂原活化蛋白激酶活性放射自显影测定方法的建立和应用[J].生物化学与生物物理进展,2001,28(3):410-414
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