Enzyme-free and rapid colorimetric analysis of osteopontin via triple-helix aptamer probe coupled with catalytic hairpin assembly reaction

被引:1
|
作者
Weng, Qin [1 ,2 ]
Li, Hang [3 ]
Fan, Zhichao [2 ]
Dong, Yan [2 ]
Qi, Yuchen [2 ]
Wang, Peilin [1 ]
Luo, Cheng [1 ]
Li, Jianjun [2 ]
Zhao, Xiang [2 ]
Yu, Hua [4 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Med & Life Sci, Chengdu 611137, Peoples R China
[2] Third Mil Med Univ, Army Med Univ, Southwest Hosp, Dept Oncol, Chongqing 400038, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Neurol, Beijing 100730, Peoples R China
[4] Hosp Chengdu Univ Tradit Chinese Med, Dept Gen Surg, Chengdu 610072, Peoples R China
关键词
Osteopontin; Triple-helix aptamer probe; Catalytic hairpin assembly; G-quadruplex/hemin DNAzyme; Hepatocellular carcinoma; LINKED-IMMUNOSORBENT-ASSAY; CANCER;
D O I
10.1016/j.aca.2024.342764
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Background: Osteopontin (OPN) is closely associated with tumorigenesis, growth, invasion, and immune escape and it serves as a plasma biomarker for hepatocellular carcinoma (HCC). Nevertheless, the accurate and rapid detection of low-abundance OPN still poses significant challenges. Currently, the majority of protein detection methods rely heavily on large precision instruments or involve complex procedures. Therefore, developing a simple, enzyme-free, rapid colorimetric analysis method with high sensitivity is imperative. Results: In this study, we have developed a portable colorimetric biosensor by integrating the triple-helix aptamer probe (THAP) and catalytic hairpin assembly (CHA) strategy, named as T-CHA. After binding to the OPN, the trigger probe can be released from THAP, then initiates the CHA reaction and outputs the signal through the formation of a G-quadruplex/Hemin DNAzyme with horseradish peroxidase-like activity. Consequently, this colorimetric sensor achieves visual free-labeled detection without additional fluorophore modification and allows for accurate quantification by measuring the optical density of the solution at 650 nm. Under optimal conditions, the logarithmic values of various OPN concentrations exhibit satisfactory linearity in the range of 5 pg mL(-1) to 5 ng mL(-1), with a detection limit of 2.04 pg mL(-1). Compared with the widely used ELISA strategy, the proposed T-CHA strategy is rapid (similar to 105 min), highly sensitive, and cost-effective. Significance: The T-CHA strategy, leveraging the low background leakage of THAP and the high catalytic efficiency of CHA, has been successfully applied to the detection of OPN in plasma, demonstrating significant promise for the early diagnosis of HCC in point-of-care testing. Given the programmability of DNA and the universality of T-CHA, it can be readily modified for analyzing other useful tumor biomarkers.
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页数:9
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