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Conjugated Polymer-Based Real-Time Fluorescence Caspase Assays

机译:基于聚合物的共轭实时荧光胱天蛋白酶测定

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We have developed conjugated polyelectrolyte-based fluorescence turn-on assays for caspase 3 and 8. These assays are composed of a cationic polyphenylene ethynylene polymer PPE4+ and p-nitroaniline modified caspase peptide substrate. The fluorescence of the assay is initially turned-off because of the efficient quenching of the polymer by p-nitroaniline moiety on anionic peptide substrates. A turn-on effect is observed due to the cleavage of the peptide by the enzyme and formation of the neutral p-nitroaniline unit which has no quenching on the polymer. We validated this assay design and obtained kinetic parameters of caspase 3 and caspase 8. These assays demonstrated good sensitivity as in pmol/L (0.1 units/ mL) for caspase 3 and nmol/L (0.2 units/mL) for caspase 8. This method also showed high specificity by using caspase 3 assay as amodel system and the results demonstrated that other proteases including caspase 8, papain, pepsin, and trypsin did not show observable fluorescence turn-on effect. The dose-response curve of a caspase inhibitor Z-VAD-FMK was evaluated by caspase 3 assay, by which the IC_(50) value was determined to be 0.73 μM and was in a good agreement with the literature reported value at 0.62 μM. This design could be applied into the in vitro screening of small molecular inhibitors for drug discovery.
机译:我们已经开发了基于共聚电解质的半胱天冬酶3和8的荧光开启测定法。这些测定法由阳离子聚亚苯基乙炔聚合物PPE4 +和对硝基苯胺修饰的半胱氨酸蛋白酶肽底物组成。由于荧光被阴离子肽底物上的对硝基苯胺部分有效地淬灭,因此测定的荧光最初被关闭。由于酶裂解了肽并形成了对聚合物没有猝灭的中性对硝基苯胺单元,因此观察到了开启效应。我们验证了该测定设计的有效性,并获得了caspase 3和caspase 8的动力学参数。这些测定证明对caspase 3的灵敏度为pmol / L(0.1单位/ mL),对caspase 8的灵敏度为nmol / L(0.2单位/ mL)。该方法还通过使用caspase 3分析作为模型系统显示出高特异性,结果表明,包括caspase 8,木瓜蛋白酶,胃蛋白酶和胰蛋白酶在内的其他蛋白酶均未显示出可观察到的荧光开启效果。通过胱天蛋白酶3测定法评估了胱天蛋白酶抑制剂Z-VAD-FMK的剂量-反应曲线,由此确定IC_(50)值为0.73μM,并与文献报道的0.62μM值良好吻合。该设计可以用于药物发现的小分子抑制剂的体外筛选。

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