Evidence map›Paper›PMID 38727732›Full record

ArticleMikrochimica acta2024

Interface-constrained catalytic hairpin assembly permits highly sensitive SERS signaling of miRNA.

Yuanqi You, Yu Ren, Yujun Li, Jianguo Xu, Zhi Li, Shuai Song, Jinxing Xia, Chenlin Shen, Jie Wang

Abstract read
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In one paragraph

Article in Mikrochimica acta, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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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

9 authors.

Yuanqi You *Inflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China.
Yu Ren *Inflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China.
Yujun LiInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China.
Jianguo XuEngineering Research Center of Bio-Process, Ministry of Education, School of Food and Biological, Hefei University of Technology, Hefei, 230009, China. jgxu0816@163.com.ORCID http://orcid.org/0000-0002-0187-2623
Zhi LiSchool of Dentistry, University of California, Los Angeles, USA.
Shuai SongInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China.
Jinxing XiaInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China.
Chenlin ShenInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China. shchlin520@163.com.
Jie WangInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Institute for Liver Diseases of Anhui Medical University, Anhui Medical University, Hefei, 230032, People's Republic of China. wangjienar@163.com.ORCID http://orcid.org/0000-0001-9954-4750

Funding

Key research and development plan of Anhui Province in 2022 2022e07020060Natural Science Foundation of Anhui Province 2308085QH303the Key Natural Science project of Anhui Provincial Education Department KJ2021A0233
6 · The paper itself

Abstract

The rapid and precise monitoring of peripheral blood miRNA levels holds paramount importance for disease diagnosis and treatment monitoring. In this study, we propose an innovative research strategy that combines the catalytic hairpin assembly reaction with SERS signal congregation and enhancement. This combination can significantly enhance the stability of SERS detection, enabling stable and efficient detection of miRNA. Specifically, our paper-based SERS detection platform incorporates a streptavidin-modified substrate, biotin-labeled catalytic hairpin assembly reaction probes, 4-ATP, and primer-co-modified gold nanoparticles. In the presence of miRNA, the 4-ATP and primer-co-modified gold nanoparticles can specifically recognize the miRNA and interact with the biotin-labeled CHA probes to initiate an interfacial catalytic hairpin assembly reaction. This enzyme-free high-efficiency catalytic process can accumulate a large amount of biotin on the gold nanoparticles, which then bind to the streptavidin on the substrate with the assistance of the driving liquid, forming red gold nanoparticle stripes. These provide a multitude of hotspots for SERS, enabling enhanced signal detection. This innovative design achieves a low detection limit of 3.47 fM while maintaining excellent stability and repeatability. This conceptually innovative detection platform offers new technological possibilities and solutions for clinical miRNA detection.

Indexed as

BiotinGoldLimit of DetectionMetal NanoparticlesMicroRNAsSpectrum Analysis, RamanCatalysisHumansStreptavidinBiotinGoldMicroRNAsStreptavidinAuNPsInterfacial catalytic hairpin assemblymiRNA detectionSERS

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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.