On-Particle Hyperbranched Rolling Circle Amplification-Scaffolded Magnetic Nanoactuator Assembly for Ferromagnetic Resonance Detection of MicroRNA

被引:0
|
作者
Fang, Yuan [1 ,2 ]
Yang, Yulin [2 ]
Yao, Ziyang [2 ]
Lei, Xi [1 ]
Dong, Zhuxin [2 ,3 ]
Zhang, Meng [1 ,4 ]
Yao, Ruifeng [1 ,4 ]
Tian, Bo [2 ,3 ]
机构
[1] Hunan Univ, Coll Biol, State Key Lab Chemo Biosensing & Chemometr, Hunan Prov Key Lab Plant Funct Genom & Dev Regulat, Changsha 410082, Peoples R China
[2] Cent South Univ, Sch Basic Med Sci, Dept Biomed Engn, Changsha 410013, Peoples R China
[3] Furong Lab, Changsha 410008, Peoples R China
[4] Hunan Univ, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金;
关键词
rotating magnetic field; magnetic nanoparticles; rolling circle amplification; microRNA detection; ferromagnetic resonance spectroscopy; CASCADE AMPLIFICATION; DNA NANOMACHINE; ACTUATION; SHAPE; SIZE;
D O I
10.1021/acssensors.3c01967
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inspired by natural molecular machines, scientists are devoted to designing nanomachines that can navigate in aqueous solutions, sense their microenvironment, actuate, and respond. Among different strategies, magnetically driven nanoactuators can easily be operated remotely in liquids and thus are valuable in biosensing. Here we report a magnetic nanoactuator swarm with rotating-magnetic-field-controlled conformational changes for reaction acceleration and target quantification. By grafting nucleic acid amplification primers, magnetic nanoparticle (MNP) actuators can assemble and be fixed with a flexible DNA scaffold generated by surface-localized hyperbranched rolling circle amplification in response to the presence of a target microRNA, osa-miR156. Net magnetic anisotropy changes of the system induced by the MNP assembly can be measured by ferromagnetic resonance spectroscopy as shifts in the resonance field. With a total assay time of ca. 120 min, the proposed biosensor offers a limit of detection of 6 fM with a dynamic detection range spanning 5 orders of magnitude. The specificity of the system is validated by testing different microRNAs and salmon sperm DNA. Endogenous microRNAs extracted from Oryza sativa leaves are tested with both quantitative reverse transcription-PCR and our approach, showing comparable performances with a Pearson correlation coefficient >0.9 (n = 20).
引用
收藏
页码:4792 / 4800
页数:9
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