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Single-labeled peptide substrates for detection of protease activity based on the inherent fluorescence quenching ability of Cu2+

机译:基于Cu2 +固有的荧光猝灭能力的用于检测蛋白酶活性的单标记肽底物

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A general peptide substrate for the specific detection of proteases is linked with a quencher/fluorophore pair. However, labeling of the substrate with a quencher/fluorophore pair may increase the complexity for the synthesis of peptides and affect the approach of protease to the cleavage site. A peptide with a specific sequence has been shown to bind Cu2+ with high affinity. More intriguingly, Cu2+ exhibits a high inherent quenching ability towards the fluorophore by complexation with the sequence-specific peptide. Based on this fact, this work reports a general single-labeled peptide substrate for the detection of protease activity, screening of potential inhibitors and evaluation of cell apoptosis. The feasibility and applications of the method were demonstrated by assays of caspase-3 and β-secretase with a signal-on and a signal-off format, respectively.
机译:用于特异性检测蛋白酶的通用肽底物与淬灭剂/荧光团对相连。但是,用淬灭剂/荧光团对标记底物可能会增加肽合成的复杂性,并影响蛋白酶到达切割位点的途径。已显示具有特定序列的肽以高亲和力结合Cu2 +。更有趣的是,Cu2 +通过与序列特异性肽复合,表现出对荧光团的高固有淬灭能力。基于这一事实,这项工作报告了一种用于检测蛋白酶活性,筛选潜在抑制剂和评估细胞凋亡的通用单标记肽底物。该方法的可行性和应用通过分别以信号开启和信号关闭形式检测caspase-3和β-分泌酶来证明。

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