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作 者:李林[1] 李国[2] 陈莉莉[3] 罗海斌[3] 陈静[3] 沈旭[3] 梅长林[1]
机构地区:[1]第二军医大学长征医院肾内科,上海200003 [2]海军411医院骨科,上海200081 [3]中国科学院上海药物研究所,上海201203
出 处:《第二军医大学学报》2009年第12期1349-1352,共4页Academic Journal of Second Military Medical University
基 金:国家自然科学基金重点项目(30330640);国家自然科学基金(30170901);国家科技部重大科技专项(2002AA2Z3130)~~
摘 要:目的:建立表皮生长因子受体(epidermal growth factor receptor,EGFR)酪氨酸激酶(receptor tyrosine kinase,RTK)抑制剂的高通量筛选模型。方法:通过基因工程技术表达EGFR-RTK,ELISA法验证其生物学活性;应用表面等离子共振原理筛选与激酶具有结合活性的化合物,ELISA法检测其生物学活性。结果:在原核表达系统中成功表达具有生物学活性的EGFR-RTK蛋白。将蛋白偶联至生物芯片,阳性化合物EI 188与EGFR酪氨酸激酶结合的Kd值为5.00×10-7mol.L-1,IC50为12.37μmol.L-1,与预期结果一致。应用该模型筛选31个待测化合物,发现了6个具有结合活性和酶抑制活性的EGFR-RTK抑制剂。结论:成功建立了基于表面等离子共振原理和ELISA法的高通量EGFR-RTK抑制剂的筛选模型,为发现新型酪氨酸激酶抑制剂奠定了基础。Objective:To establish a high throughput screening(HTS) model for epidermal growth factor(EGF) receptor tyrosine kinase(RTK) inhibitor.Methods: The bioactive EGFR-RTK was expressed by genetic engineering technology.The binding activity and bioactivity of the compounds were examined by surface plasmon resonance and ELISA.Results: The bioactive EGFR-RTK protein was successfully expressed in the prokaryotic expression system and was immobilized on the sensor chip.The equilibrium constants(Kd) between TKI(EI 188) and RTK was 5.00×10^-7 mol·L^-1,and the IC50 was 12.37 μmol·L^-1,which was consistent with expected.With this model we screened 31 compounds and found that 6 compounds had binding activity and inhibitory activity.Conclusion: A novel HTS model of EGFR-TKI has been successfully established using surface plasmon resonance biosensor and ELISA,which lays a foundation for discovery of new TKIs.
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