生物正交化学
癌胚抗原
免疫分析
细菌
生物传感器
组合化学
荧光
检出限
材料科学
色谱法
化学
纳米技术
点击化学
生物
抗体
癌症
物理
免疫学
量子力学
遗传学
作者
Yanfeng Gao,Dongtao Zhou,Qin Xu,Jingjing Li,Wen Luo,Jingjing Yang,Yongchun Pan,Ting Huang,Yanping Wang,Bangshun He,Yujun Song,Yuzhen Wang
标识
DOI:10.1021/acsami.2c21350
摘要
Ultrasensitive quantification of protein biomarkers has significant implications in disease diagnosis. Herein, we report a fluorescent bacteria counting immunoassay (FBCIA) strategy for protein biomarker detection based on a cascade signal conversion and amplification strategy including the copper metal–organic framework (Cu-MOF)-mediated Cu(I)-catalyzed azide–alkyne cycloaddition (CuAAC) for fluorescent bacteria immobilization that converted the concentration of target protein to countable bacterial number and the further self-proliferation of bacteria to amplify the detectable bacterial number. The developed low-background and enzyme-free cascade methodology achieved highly sensitive detection of carcinoembryonic antigen (CEA) and prostate-specific antigen (PSA) with detection limits down to 0.8 pg/mL and 64.5 fg/mL, respectively. On top of that, we also developed a smartphone device for visualizing individual bacteria and point-of-care counting of the resulting bacteria for the detection of clinical samples. The good consistency between FBCIA and clinical enzyme-linked immunosorbent assay (ELISA) validated the high reliability and promising potential of our developed platform in clinical applications.
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