Metal-organic frameworks-assisted nonenzymatic cascade amplification multiplexed strategy for sensing acute myocardial infarction related microRNAs

被引:30
作者
Cheng, Xia [1 ]
Ren, Dandan [1 ]
Xu, Guanhong [1 ,2 ]
Wei, Fangdi [1 ,2 ]
Yang, Jing [1 ,2 ]
Xu, Jian [3 ]
Wang, Lin [3 ]
Hu, Qin [1 ,2 ]
Cen, Yao [1 ,2 ]
机构
[1] Nanjing Med Univ, Sch Pharm, Nanjing 211166, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Sch Pharm, Key Lab Cardiovasc & Cerebrovasc Med, Nanjing 211166, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Lab Med, Affiliated Hosp 1, Nanjing 211166, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Acute myocardial infarction; Multiple microRNA detection; Signal amplification; Simultaneous detection; Metal-organic frameworks; ULTRASENSITIVE DETECTION; DNA; BIOMARKERS;
D O I
10.1016/j.bios.2021.113706
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Amplification strategies for multiple microRNAs (miRNAs) detection are pivotal for acute myocardial infarction (AMI). Herein, we rationally developed a metal-organic frameworks-assisted nonenzymatic cascade amplification strategy for simultaneous quantification of three AMI-related miRNAs (miR-21, miR-499 and miR-133a). The fluorescence of the elaborately designed DNA molecular beacons with the respective modification of FAM, TAMRA and Cy5 in the terminal was quenched by a metal-organic framework named Fe-MIL-88. When targets miRNA appeared, they hybridized with the corresponding DNA molecular beacons, and the catalyzed hairpin assembly (CHA) reaction would be triggered, producing "Y" shaped three-branched duplex nanostructure with the targets released, and initiating subsequent another cycle. The "Y" shaped nanostructures could not be adsorbed onto the surface of Fe-MIL-88 due to the weaker affinity between Fe-MIL-88 and "Y" shaped nano structures. Therefore, the fluorescence of "Y" shaped nanostructures could not be quenched by Fe-MIL-88. In this way, three AMI-related miRNAs were simultaneously detected in the respective ranges of 0.05-30 nM, 0.08-30 nM and 0.1-20 nM with respective limits of detection down to 13, 25 and 40 pM. Furthermore, the method was successfully employed to determine three AMI-related miRNAs in human serum. The strategy offered great opportunity for ultrasensitive detecting multiple AMI-related miRNAs and substantially improving the accuracy of clinical early AMI diagnosis.
引用
收藏
页数:6
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