A novel DNA biosensor for ultrasensitive detection of DNA methyltransferase activity based on a high-density “hot spots” SERS substrate and rolling circle amplification strategy

The Analyst ◽  
2021 ◽  
Author(s):  
Shengjie Ge ◽  
Menglin Ran ◽  
Yu Mao ◽  
Yue Sun ◽  
Xinyu Zhou ◽  
...  

Herein, we proposed a novel biosensor based on the high-density “hot spots” Au@SiO2 array substrate and rolling circle amplification (RCA) strategy for ultrasensitive detection of the CpG methyltransferase (M.SssI) activity....

2016 ◽  
Vol 52 (12) ◽  
pp. 2517-2520 ◽  
Author(s):  
Haiyan Zhao ◽  
Lei Wang ◽  
Wei Jiang

A novel fluorescence detection system is developed for DNA methyltransferase activity assay based on target-protected dumbbell molecular probe mediated cascade rolling circle amplification strategy.


2014 ◽  
Vol 50 (13) ◽  
pp. 1576-1578 ◽  
Author(s):  
Liang Cui ◽  
Zhi Zhu ◽  
Ninghang Lin ◽  
Huimin Zhang ◽  
Zhichao Guan ◽  
...  

A T7 exonuclease-assisted cyclic enzymatic amplification method (CEAM) was combined with rolling circle amplification (RCA) to develop a RCA–CEAM dual amplification method for ultrasensitive detection of microRNA with excellent selectivity.


2014 ◽  
Vol 25 (7) ◽  
pp. 1047-1051 ◽  
Author(s):  
Pei Liu ◽  
Xiao-Hai Yang ◽  
Qing Wang ◽  
Jing Huang ◽  
Jian-Bo Liu ◽  
...  

2019 ◽  
Vol 10 (8) ◽  
pp. 2290-2297 ◽  
Author(s):  
Yun-Xi Cui ◽  
Xue-Nan Feng ◽  
Ya-Xin Wang ◽  
Hui-Yu Pan ◽  
Hua Pan ◽  
...  

An ultra-sensitive biosensor using only two DNA oligos to initiate multiple signal amplification cycles.


Biosensors ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 222
Author(s):  
Chenxin Fang ◽  
Ping Ouyang ◽  
Yuxing Yang ◽  
Yang Qing ◽  
Jialun Han ◽  
...  

A microRNA (miRNA) detection platform composed of a rolling circle amplification (RCA) system and an allosteric deoxyribozyme system is proposed, which can detect miRNA-21 rapidly and efficiently. Padlock probe hybridization with the target miRNA is achieved through complementary base pairing and the padlock probe forms a closed circular template under the action of ligase; this circular template results in RCA. In the presence of DNA polymerase, RCA proceeds and a long chain with numerous repeating units is formed. In the presence of single-stranded DNA (H1 and H2), multi-component nucleic acid enzymes (MNAzymes) are formed that have the ability to cleave substrates. Finally, substrates containing fluorescent and quenching groups and magnesium ions are added to the system to activate the MNAzyme and the substrate cleavage reaction, thus achieving fluorescence intensity amplification. The RCA–MNAzyme system has dual signal amplification and presents a sensing platform that demonstrates broad prospects in the analysis and detection of nucleic acids.


RSC Advances ◽  
2014 ◽  
Vol 4 (51) ◽  
pp. 27091-27097 ◽  
Author(s):  
Qingwang Xue ◽  
Yanqin Lv ◽  
Yuanfu Zhang ◽  
Shuling Xu ◽  
Qiaoli Yue ◽  
...  

A novel label-free amplified fluorescent sensing scheme based on target-responsive dumbbell probe-mediated rolling circle amplification (D-RCA) has been developed for sensitive and selective detection of mercuric ions.


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