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A ratiometric fluorescent biosensor based on self-fluorescent MOF and target-triggered rolling circle amplification for sensitive detection of exosome-derived miRNA
被引:26
|作者:
Sun, Zhiwei
[1
,2
]
Li, Juan
[3
]
Tong, Yao
[3
]
Han, Hecheng
[1
]
Yang, Yufei
[1
]
Wang, Chuanxin
[3
,4
,5
]
Li, Hui
[1
]
Du, Lutao
[1
,3
]
Jiang, Yanyan
[1
,2
]
机构:
[1] Shandong Univ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jinan 250061, Peoples R China
[2] Shenzhen Res Inst Shandong Univ, Shenzhen 518057, Peoples R China
[3] Shandong Univ, Hosp 2, Cheeloo Coll Med, Dept Clin Lab, Jinan 250033, Peoples R China
[4] Shandong Engn & Technol Res Ctr Tumor Marker Detec, Jinan 250033, Peoples R China
[5] Shandong Prov Clin Med Res Ctr Clin Lab, Jinan 250033, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Ratiometric fluorescence;
Biosensor;
Exosomal miRNAs;
Metal -organic framework;
Rolling circle amplification;
METAL-ORGANIC FRAMEWORK;
PLATFORM;
D O I:
10.1016/j.aca.2022.340136
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
MicroRNAs (miRNAs) are considered as biomarkers and display great potential in the diagnosis of diseases. As a colorectal cancer (CRC)-associated miRNA biomarker, miR-92a-3p possesses higher concentration in exosomes than in serum, causing it more feasible to diagnose CRC by measuring the concentration of miR-92a-3p inside exosomes. Herein, a rationally-engineered ratiometric fluorescent biosensor is proposed to detect the concentration of exosomal miR-92a-3p. The metal-organic framework (MOF-525) with self-fluorescence serves as both a fluorescent reference and a quencher of the fluorescence of single-stranded reporter by adsorption. The presence of miR-92a-3p triggers the looping of 5P-template strand and the further periodic rolling circle amplification. The periodic long strands and the reporters can form double strands to prevent the reporters from being adsorbed by MOF-525. The concentration of miR-92a-3p is positively correlated with the Delta reporter/MOF-525 fluorescence intensity ratio. The biosensor exhibits a detection range of 0.1-10 pM and can differentiate miR-92a-3p from mismatched RNA sequences. The accuracy and practicality of the proposed biosensor for exosomal miRNA
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