Evidence map›Paper›PMID 33310991›Full record

ArticleAnalytical sciences : the international journal of the Japan Society for Analytical Chemistry2021

Polymerase/Nicking Enzyme Powered Dual-template Multi-cycle G-Triplex Machine for HIV-1 Determination.

Gang Yi, Qiuyue Duan, Qi Yan, Yuqi Huang, Wenxiu Zhang, Shuhui Zhao

Abstract read
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In one paragraph

Article in Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. PhotocleavableChemical reviews · 2023
    Review
  3. Types and Applications of Nicking Enzyme-Combined Isothermal Amplification.International journal of molecular sciences · 2022
    Review
  4. A molecular beacon-like Ag nanocluster fluorescence probe for nucleic acid detection.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2022
    Article
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

6 authors.

Gang YiKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China. yigang666@cqmu.edu.cn.
Qiuyue DuanKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China.
Qi YanKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China.
Yuqi HuangKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China.
Wenxiu ZhangKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China.
Shuhui ZhaoKey Laboratory of Clinical Laboratory Diagnostics (Ministry of Education of China), Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We proposed a dual-template, multi-cycle DNA nanomachine driven by polymerase and a nicking enzyme with high efficiency. The reaction system simply consists of two templates (T1, T2) and two enzymes (KF polymerase, Nb.BbvCI). The two templates are similar in structure (X-X'-Y, Y-Y'-C) with a primer recognition region, a primer analogue generation region, an output region (3'-5'), and two nicking sites. The output strand of T1 is the primer of T2, and the G-rich fragment (G3) is designed as the final product. In the presence of HIV-1, numerous G3 were generated through the multi-cycle amplification strategy and formed a G-triplex/ThT complex after the addition of thioflavin T (ThT), which greatly enhanced the fluorescence intensity as a signal reporter in the label-free sensing strategy. A dynamic response range of 50 fM - 2 nM for HIV-1 gene detection can be achieved through this multi-cycle G-triplex machine, and benefiting from the high efficiency amplification strategy, the enzymatic reaction can be completed within 45 min and followed by fluorescence measurements. In addition, the analysis of other targets can be achieved by replacing the template sequence. Thus, there is a certain application potential of this strategy for trace biomarker analysis.

Indexed as

Biosensing TechniquesHIV-1DNALimit of DetectionNucleic Acid Amplification TechniquesSpectrometry, FluorescenceDNADNA machinefluorescenceHIVmulti-cycle amplificationtrace biomarker analysis

Identifiers

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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.