School of Life Sciences, Central South University, Changsha 410013, China.
Molecules. 2022 Sep 18;27(18):6093. doi: 10.3390/molecules27186093.
A novel, label-free fluorescent assay has been developed for the detection of trypsin by using thioflavin T as a fluorescent probe. A specific DNA aptamer can be combined by adding cytochrome c. Trypsin hydrolyzes the cytochrome c into small peptide fragments, exposing the G-quadruplex part of DNA aptamer, which has a high affinity for thioflavin T, which then enhances the fluorescence intensity. In the absence of trypsin, the fluorescence intensity was inhibited as the combination of cytochrome c and the DNA aptamer impeded thioflavin T's binding. Thus, the fluorescent biosensor showed a linear relationship from 0.2 to 60 μg/mL with a detection limit of 0.2 μg/mL. Furthermore, the proposed method was also successfully employed for determining trypsin in biological samples. This method is simple, rapid, cheap, and selective and possesses great potential for the detection of trypsin in bioanalytical and biological samples and medical diagnoses.
一种新型的、无标记的荧光分析方法已经被开发出来,用于检测胰蛋白酶,使用的荧光探针是硫黄素 T。通过添加细胞色素 c,可以结合特定的 DNA 适体。胰蛋白酶将细胞色素 c 水解成小肽片段,暴露出 DNA 适体的 G-四链体部分,它与硫黄素 T 具有高亲和力,从而增强了荧光强度。在没有胰蛋白酶的情况下,由于细胞色素 c 和 DNA 适体的结合阻碍了硫黄素 T 的结合,荧光强度受到抑制。因此,荧光生物传感器在 0.2 至 60 μg/mL 的范围内呈现出线性关系,检测限为 0.2 μg/mL。此外,该方法还成功地用于测定生物样品中的胰蛋白酶。该方法简单、快速、廉价、选择性好,在生物分析和生物样品以及医学诊断中检测胰蛋白酶具有很大的潜力。