Liu Fang, Yang Min, Song Wenlu, Luo Xingyu, Tang Rui, Duan Zhixi, Kang Wenyuan, Xie Shiyi, Liu Qingqing, Lei Chunyang, Huang Yan, Nie Zhou, Yao Shouzhuo
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
Department of Orthopedics, The Second Xiangya Hospital, Central South University Changsha 410011 Hunan P. R. China.
Chem Sci. 2020 Feb 10;11(11):2993-2998. doi: 10.1039/c9sc04692e.
Signal amplification is an effective way to achieve sensitive analysis of biomarkers, exhibiting great promise in biomedical research and clinical diagnosis. Inspired by the transcription process, here we present a versatile strategy that enables effective amplification of proteolysis into nucleic acid signal outputs in a homogeneous system. In this strategy, a protease-activatable T7 RNA polymerase is engineered as the signal amplifier and achieves 3 orders of magnitude amplification in signal gain. The versatility of this strategy has been demonstrated by the development of sensitive and selective assays for protease biomarkers, such as matrix metalloproteinase-2 (MMP-2) and thrombin, with sub-picomole sensitivity, which is 4.3 × 10-fold lower than that of the standard peptide-based method. Moreover, the proposed assay has been further applied in the detection of MMP-2 secreted by cancer cells, as well as in the assessment of MMP-2 levels in osteosarcoma tissue samples, providing a general approach for the monitoring of protease biomarkers in clinical diagnosis.
信号放大是实现生物标志物灵敏分析的有效方法,在生物医学研究和临床诊断中展现出巨大潜力。受转录过程启发,我们在此提出一种通用策略,可在均相体系中将蛋白水解有效地放大为核酸信号输出。在该策略中,一种蛋白酶可激活的T7 RNA聚合酶被设计为信号放大器,信号增益实现了3个数量级的放大。通过开发针对蛋白酶生物标志物(如基质金属蛋白酶-2(MMP-2)和凝血酶)的灵敏且选择性的检测方法,已证明了该策略的通用性,其灵敏度达到亚皮摩尔级,比基于标准肽的方法低4.3×10倍。此外,所提出的检测方法已进一步应用于癌细胞分泌的MMP-2的检测,以及骨肉瘤组织样本中MMP-2水平的评估,为临床诊断中监测蛋白酶生物标志物提供了一种通用方法。