DNA nanostructures from palindromic rolling circle amplification for the fluorescent detection of cancer-related microRNAs

Talanta ◽  
2019 ◽  
Vol 192 ◽  
pp. 175-181 ◽  
Author(s):  
Huo Xu ◽  
Shuxin Zhang ◽  
Changhe Ouyang ◽  
Zhenmeng Wang ◽  
Dong Wu ◽  
...  
2015 ◽  
Vol 51 (12) ◽  
pp. 2392-2395 ◽  
Author(s):  
Weiling Song ◽  
Qiao Zhang ◽  
Wenbo Sun

An ultrasensitive protocol for fluorescent detection of DNA is designed by combining the template enhanced hybridization process (TEHP) with Rolling Circle Amplification (RCA) and Catalytic Hairpin Assembly (CHA), showing a remarkable amplification efficiency.


2014 ◽  
Vol 50 (86) ◽  
pp. 13049-13051 ◽  
Author(s):  
Cheol Am Hong ◽  
Bora Jang ◽  
Eun Hye Jeong ◽  
Hansaem Jeong ◽  
Hyukjin Lee

Large-scale preparation of DNA nanostructures for siRNA delivery has been achieved by an isothermal enzymatic amplification process.


2018 ◽  
Vol 410 (26) ◽  
pp. 6819-6826 ◽  
Author(s):  
Zhihua Gao ◽  
Chengwei Wu ◽  
Sha Lv ◽  
Cong Wang ◽  
Nan Zhang ◽  
...  

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Tomoya Yata ◽  
Yuki Takahashi ◽  
Mengmeng Tan ◽  
Kumi Hidaka ◽  
Hiroshi Sugiyama ◽  
...  

Abstract The application of DNA as a functional material such as DNA hydrogel has attracted much attention. Despite an increasing interest, the high cost of DNA synthesis is a limiting factor for its utilization. To reduce the cost, we report here a highly efficient amplification technique for polypod-like structured DNA (polypodna) with adhesive ends that spontaneously forms DNA hydrogel. Two types of polypodna with three (tripodna) and four (tetrapodna) pods were selected and a template oligodeoxynucleotide, containing a tandem sequence of a looped tripodna or tetrapodna, respectively, along with restriction enzyme (TspRI) sites, was designed. The template was circularized using T4 DNA ligase and amplified by rolling circle amplification (RCA). The RCA product was highly viscous and resistant to restriction digestion. Observation under an electron microscope revealed microflower-like structures. These structures were composed of long DNA and magnesium pyrophosphate and their treatment with EDTA followed by restriction digestion with TspRI resulted in numerous copies of polypodna with adhesive ends, which formed a DNA hydrogel. Thus, we believe this technique provides a new approach to produce DNA nanostructures and helps in expanding their practical applications.


2017 ◽  
Author(s):  
Bo Tian ◽  
Peter Svedlindh ◽  
Mattias Strömberg ◽  
Erik Wetterskog

In this work, we demonstrate for the first time, a ferromagnetic resonance (FMR) based homogeneous and volumetric biosensor for magnetic label detection. Two different isothermal amplification methods, <i>i.e.</i>, rolling circle amplification (RCA) and loop-mediated isothermal amplification (LAMP) are adopted and combined with a standard electron paramagnetic resonance (EPR) spectrometer for FMR biosensing. For RCA-based FMR biosensor, binding of RCA products of a synthetic Vibrio cholerae target DNA sequence gives rise to the formation of aggregates of magnetic nanoparticles. Immobilization of nanoparticles within the aggregates leads to a decrease of the net anisotropy of the system and a concomitant increase of the resonance field. A limit of detection of 1 pM is obtained with an average coefficient of variation of 0.16%, which is superior to the performance of other reported RCA-based magnetic biosensors. For LAMP-based sensing, a synthetic Zika virus target oligonucleotide is amplified and detected in 20% serum samples. Immobilization of magnetic nanoparticles is induced by their co-precipitation with Mg<sub>2</sub>P<sub>2</sub>O<sub>7</sub> (a by-product of LAMP) and provides a detection sensitivity of 100 aM. The fast measurement, high sensitivity and miniaturization potential of the proposed FMR biosensing technology makes it a promising candidate for designing future point-of-care devices.<br>


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