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首页> 外文期刊>Analytical Sciences >A Label-free Fluorescence Assay for Trypsin Based on the Electron Transfer between Oligonucleotide-stabilized Ag Nanoclusters and Cytochrome c
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A Label-free Fluorescence Assay for Trypsin Based on the Electron Transfer between Oligonucleotide-stabilized Ag Nanoclusters and Cytochrome c

机译:基于寡核苷酸稳定的Ag纳米团簇和细胞色素c之间电子转移的胰蛋白酶无标记荧光测定

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A label-free fluorescent assay for the detection of trypsin by using oligonucleotide-templated silver nanoclusters (Ag NCs) and cytochrome c (Cyt c) has been demonstrated. When negatively charged Ag NCs and positively charged Cyt c are mixed, they tend to form a hybrid complex, and then lead the fluorescence of Ag NCs to be quenched significantly due to electron transfer between Ag NCs and the heme cofactor of Cyt c. In the presence of trypsin, it catalyzes the hydrolytic cleavage of Cyt c to small peptide fragments, and releases the heme moiety from the Ag NCs/Cyt c complex; the quenched fluorescence restores therewith. By virtue of this specific response, the fluorescent biosensor has a linear range of from 0.7 to 4 μg mL~(?1) and from 9 to 120 μg mL~(?1) with a detection limit of 58.7 ng mL~(?1). Aside from the easy manufacture aspect, our method also possesses a high signal-to-background ratio (~11), excellent selectivity and good biocompatibility, which makes it a promising bioanalysis for a trypsin activity assay.
机译:通过使用寡核苷酸模板化的银纳米簇(Ag NCs)和细胞色素c(Cyt c),已证明了无标记荧光检测胰蛋白酶的方法。当带负电的Ag NCs和带正电的Cyt c混合时,它们趋于形成杂化复合物,然后由于Ag NCs与Cyt c的血红素辅因子之间的电子转移,导致Ag NCs的荧光显着淬灭。在胰蛋白酶存在下,它催化Cyt c水解裂解成小的肽片段,并从Ag NCs / Cyt c复合物中释放血红素部分。淬灭的荧光随之恢复。凭借这种特定的响应,荧光生物传感器的线性范围为0.7至4μgmL〜(?1)和9至120μgmL〜(?1),检测极限为58.7 ng mL〜(?1 )。除了易于制造之外,我们的方法还具有较高的信噪比(〜11),优异的选择性和良好的生物相容性,这使其成为有希望的胰蛋白酶活性测定生物分析方法。

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