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Investigation of effects of newly synthesized Pt(II) complex against human serum albumin and leukemia cell line of K562

机译:新合成的Pt(II)配合物对人血清白蛋白和白血病细胞株K562作用的研究

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The biological evaluation of a new synthesized Pt(II)-complex, 2,2'-bipyridin Butylglycinato Pt(II) nitrate, an anti-tumor component, was studied at different temperatures by fluorescence and far UV circular dichroism (CD) spectroscopic methods. Human serum albumin (HSA) and human tumor cell line K562 were as targets. The Pt(II)-complex has a strong ability to quench the intrinsic fluorescence of HSA. Binding and thermodynamic parameters of the interaction were calculated by fluorescence quenching method. Far-UV-CD results showed that Pt(II)-complex induced increasing in content of a helical structure of the protein and stabilized it. The 50% cytotoxic concentration (Cc(50)) of complex was determined using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay at different incubation times. Also, fluorescence staining with DAPI (4,6-diamidino-2-phenylindole) revealed some typical nuclear changes, which are characteristic of apoptosis. Above results suggest that Pt (II) complex is a promising anti-proliferative agent and should execute its biological effects by inducing apoptosis. [BMB reports 2010; 43(11): 766-771]
机译:通过荧光和远紫外圆二色性(CD)光谱方法研究了一种新合成的Pt(II)络合物2,2'-联吡啶丁基氨基甘氨酸对硝酸Pt(II)的生物学评价。 。以人血清白蛋白(HSA)和人肿瘤细胞系K562为靶标。 Pt(II)复合物具有很强的淬灭HSA固有荧光的能力。通过荧光猝灭法计算相互作用的结合力和热力学参数。远紫外线CD结果表明,Pt(II)络合物诱导蛋白质螺旋结构的含量增加并使其稳定。使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑鎓)测定法在不同的孵育时间下测定复合物的50%细胞毒性浓度(Cc(50))。同样,用DAPI(4,6-二mid基-2-苯基吲哚)进行荧光染色显示了一些典型的核变化,这是凋亡的特征。以上结果表明,Pt(II)复合物是一种有前途的抗增殖剂,应通过诱导细胞凋亡来发挥其生物学作用。 [BMB报告2010; 43(11):766-771]

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