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用于蛋白酪氨酸激酶抑制剂高通量筛选的均相时间分辨荧光免疫方法的建立
引用本文:李旭桂,王广发,张俊艳,吴少瑜,徐伟,吴曙光,张嘉杰. 用于蛋白酪氨酸激酶抑制剂高通量筛选的均相时间分辨荧光免疫方法的建立[J]. 南方医科大学学报, 2009, 29(8): 1612
作者姓名:李旭桂  王广发  张俊艳  吴少瑜  徐伟  吴曙光  张嘉杰
作者单位:南方医科大学药学院,广东,广州,510515
基金项目:广州市粤港关键领域重点突破项目
摘    要:目的 建立一种均相时间分辨荧光免疫分析方法用于蛋白酪氨酸激酶抑制剂的体外高通量筛选.方法 根据铕联穴状化合物(EuK)和异藻蓝蛋白(XL-665)两个荧光化合物在激发后的能量共振转移所发出的特异性荧光,采用多功能酶标仪在波长为612 nm和670 nm处测定荧光信号的变化;以血管内皮生长因子2(VEGFR-2)为蛋白酪氨酸激酶,检测蛋白酪氨酸激酶抑制剂Sunitinib的抑制活性.结果 建立了一种用于蛋白酪氨酸激酶抑制剂体外高通量筛选的均相时间分辨荧光免疫分析方法.在反应体系中,蛋白酪氨酸激酶VEGFR-2、三磷酸腺苷(ATP)和多肽底物浓度分别为5ng/μ1、100 μmol/L和1 μmol/L.在上述条件下,检测到Sunitinib 对 VEGFR-2酪氨酸激酶抑制活性的IC_(50)为86.7nmol/L,与文献报道的结果近似.结论 本实验所建立的均相时间分辨荧光免疫分析方法操作简便,重复性好,可用于蛋白酪氨酸激酶抑制剂的体外高通量筛选.
Abstract:
Objective To establish an in vitro homogeneous time-resolved fluorescence immunoassay method for high throughput screening of protein tyrosine kinase (PTK) inhibitors. Methods Specific fluorescence signals at 670 and 612 nm were measured by multifunctional microplate reader when the fluorescence was emitted through a resonance energy transfer between fluorescent materials (EuK and XL-665). The inhibitory activity of Sunitinib, a standard PTK inhibitor, on vascular endothelia growth factor receptor 2 (VEGFR-2) kinase activity was investigated. Results A homogeneous time-resolved fluorescence immunoassay was established for high throughput screening of PTK inhibitor. In this system, the concentrations of VEGFR-2, adenosine triphosphate (ATP) and poly-peptide substrate were 5 ng/μ1, 100 μmol/L and 1 μmol/L,respectively. Sunitinib inhibited VEGFR-2 kinase activity with an IC_(50) value of 86.7 nmol/L, which was close to the values tested using other methods. Conclusion The homogeneous time-resolved fluorescence immunoassay we established can be easily used for high throughput screening of PTK inhibitors.

关 键 词:蛋白酪氨酸激酶  时间分辨荧光免疫分析  血管内皮生长因子受体2

Establishment of homogeneous time-resolved fluorescence immunoassay for high throughput screening of protein tyrosine kinase inhibitors
LI Xu-gui,WANG Guang-fa,ZHANG Jun-yan,WU Shao-yu,XU Wei,WU Shu-guang,ZHANG Jia-jie. Establishment of homogeneous time-resolved fluorescence immunoassay for high throughput screening of protein tyrosine kinase inhibitors[J]. Journal of Southern Medical University, 2009, 29(8): 1612
Authors:LI Xu-gui  WANG Guang-fa  ZHANG Jun-yan  WU Shao-yu  XU Wei  WU Shu-guang  ZHANG Jia-jie
Affiliation:LI Xu-gui,WANG Guang-fa,ZHANG Jun-yan,WU Shao-yu,XU Wei,WU Shu-guang,ZHANG Jia-jie School of Pharmaceutical Sciences,Southern Medical University,Guangzhou 510515,China
Abstract:Objective To establish an in vitro homogeneous time-resolved fluorescence immunoassay method for high throughput screening of protein tyrosine kinase (PTK) inhibitors. Methods Specific fluorescence signals at 670 and 612 nm were measured by multifunctional microplate reader when the fluorescence was emitted through a resonance energy transfer between fluorescent materials (EuK and XL-665). The inhibitory activity of Sunitinib, a standard PTK inhibitor, on vascular endothelia growth factor receptor 2 (VEGFR-...
Keywords:protein-tyrosine kinases  vascular endothelia growth factor receptor 2  time-resolved immunofluorometric assay  
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