State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha 410082, P. R. China.
Anal Chem. 2020 Dec 15;92(24):16314-16321. doi: 10.1021/acs.analchem.0c04427. Epub 2020 Dec 1.
Proteases play crucial roles in the malignant progression of tumor and thus have been regarded as biomarkers for many cancers. Although protease assays such as immunoassays and fluorogenic substrate probes have been developed, it remains challenging for them to give consideration to both sensitivity and accuracy. Here, we describe a proteolysis-responsive rolling circle transcription assay (PRCTA) for the ultrasensitive and accurate detection of protease activities by the rational integration of a protease-responsive RNA polymerase and rolling circle transcription. Taking cancer biomarker matrix metalloproteinase-2 (MMP-2) as the model, the PRCTA, which can transduce and amplify each proteolysis event catalyzed by MMP-2 into the output of multiple tandem fluorescent RNAs by transcription, is constructed for the sensitive analysis of MMP-2 activities. Such a rational integration greatly enhances the signal gain in PRCTA, and it enables the limit of detection of MMP-2 as low as 3 fM. The feasibility of PRCTA has been validated by the sensitive analysis of cellular MMP-2 activities of different cell lines with good accuracy, and the readout can be readily visualized by a fluorescence imaging system. Therefore, PRCTA has achieved the detection of target protease biomarkers with femtomolar sensitivity, exhibiting promising potential in biomedicine research and cancer diagnosis.
蛋白酶在肿瘤的恶性进展中起着至关重要的作用,因此被认为是许多癌症的生物标志物。尽管已经开发出了免疫测定和荧光底物探针等蛋白酶测定法,但它们在兼顾灵敏度和准确性方面仍然具有挑战性。在这里,我们描述了一种基于酶切反应的滚环转录分析(PRCTA),通过合理整合对蛋白酶反应的 RNA 聚合酶和滚环转录,实现了对蛋白酶活性的超灵敏和准确检测。以癌症生物标志物基质金属蛋白酶-2(MMP-2)为例,该 PRCTA 可以将 MMP-2 催化的每个酶切事件转化为多个串联荧光 RNA 的转录输出,用于 MMP-2 活性的灵敏分析。这种合理的整合极大地提高了 PRCTA 的信号增益,使其能够检测到低至 3 fM 的 MMP-2。通过对不同细胞系的细胞 MMP-2 活性进行灵敏分析,验证了 PRCTA 的可行性,并且可以通过荧光成像系统轻松可视化读数。因此,PRCTA 以飞摩尔灵敏度实现了对靶蛋白酶生物标志物的检测,在生物医学研究和癌症诊断方面具有广阔的应用前景。