Evidence map›Paper›PMID 31812164›Full record

ArticleJournal of nanobiotechnology2019

A novel fluorescent biosensor based on dendritic DNA nanostructure in combination with ligase reaction for ultrasensitive detection of DNA methylation.

Shu Zhang, Jian Huang, Jingrun Lu, Min Liu, Yan Li, Lichao Fang, Hui Huang, Jianjun Huang, Fei Mo, Junsong Zheng

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Current Advances in DNA Methylation Analysis Methods.BioMed research international · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Shu ZhangDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China.
Jian HuangCenter for Clinical Laboratories, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
Jingrun LuCenter for Clinical Laboratories, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
Min LiuCenter for Clinical Laboratories, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
Yan LiDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China.
Lichao FangDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China.
Hui HuangDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China.
Jianjun HuangDepartment of Breast Surgery, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
Fei MoDepartment of Basic Clinical Laboratory Medicine, School of Clinical Laboratory Science, Guizhou Medical University, Guiyang, 550004, China. mofei@gmc.edu.cn.
Junsong ZhengDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China. zhengalpha@tmmu.edu.cn.ORCID http://orcid.org/0000-0002-5248-4209
Guiyang Medical University · CNArmy Medical University · CN

Funding

Army Innovation Research Project LJ20182B060005China Postdoctoral Science Foundation 2018M643862National Natural Science Foundation of China 81401722National Natural Science Foundation of China 81572078National Natural Science Foundation of China 81860723National Natural Science Foundation of China 8186140341National Natural Science Foundation of China 8187081672National Natural Science Foundation of China 81873982The Projects of Basic Research and Frontier Exploration in Chongqing cstc2019jcyj-zdxm0037The Third Military Medical University Medical Creative Research Foundation SWH2016JCYB-33The Third Military Medical University Medical Creative Research Foundation SWH2016JCYB-62Traditional Chinese Medicine, National Medicine Science and Technology Fund QZYY-2018-019
6 · The paper itself

Abstract

backgroundDNA methylation detection is indispensable for the diagnosis and prognosis of various diseases including malignancies. Hence, it is crucial to develop a simple, sensitive, and specific detection strategy.

methodsA novel fluorescent biosensor was developed based on a simple dual signal amplification strategy using functional dendritic DNA nanostructure and signal-enriching polystyrene microbeads in combination with ligase detection reaction (LDR). Dendritic DNA self-assembled from Y-DNA and X-DNA through enzyme-free DNA catalysis of a hairpin structure, which was prevented from unwinding at high temperature by adding psoralen. Then dendritic DNA polymer labeled with fluorescent dye Cy5 was ligated with reporter probe into a conjugate. Avidin-labeled polystyrene microbeads were specifically bound to biotin-labeled capture probe, and hybridized with target sequence and dendritic DNA. LDR was triggered by adding Taq ligase. When methylated cytosine existed, the capture probe and reporter probe labeled with fluorescent dye perfectly matched the target sequence, forming a stable duplex to generate a fluorescence signal. However, after bisulfite treatment, unmethylated cytosine was converted into uracil, resulting in a single base mismatch. No fluorescence signal was detected due to the absence of duplex.

resultsThe obtained dendritic DNA polymer had a large volume. This method was time-saving and low-cost. Under the optimal experimental conditions using avidin-labeled polystyrene microbeads, the fluorescence signal was amplified more obviously, and DNA methylation was quantified ultrasensitively and selectively. The detection range of this sensor was 10

conclusionThis strategy has ultrasensitivity and high specificity for DNA methylation quantification, without requiring complex processes such as PCR and enzymatic digestion, which is thus of great value in tumor diagnosis and biomedical research.

Indexed as

DNA MethylationBiosensing TechniquesCell Line, TumorCpG IslandsDNAHumansNanostructuresSpectrometry, FluorescenceDNACatalyzed hairpin assemblyDendritic DNADNA methylationFluorescent biosensorLigation detection reaction

Identifiers

PMID31812164
PMCPMC6898925
OpenAlexW2994085198

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.