Absolute quantification of microRNAs based on mass transport limitation under a laminar flow SPR system

IF 10.7 1区 生物学 Q1 BIOPHYSICS Biosensors and Bioelectronics Pub Date : 2023-11-06 DOI:10.1016/j.bios.2023.115776
Kai Li , Na An , Liqing Wu , Min Wang , Fukai Li , Liang Li
{"title":"Absolute quantification of microRNAs based on mass transport limitation under a laminar flow SPR system","authors":"Kai Li ,&nbsp;Na An ,&nbsp;Liqing Wu ,&nbsp;Min Wang ,&nbsp;Fukai Li ,&nbsp;Liang Li","doi":"10.1016/j.bios.2023.115776","DOIUrl":null,"url":null,"abstract":"<div><p>As an important biomarker for diagnostics and therapeutics of various diseases, the low-cost, quantitative detection method of microRNAs (miRNAs) has recently caught broad attention. However, their small size and low abundance still derive challenges to quantification detection. In this study, we developed an ultrasensitive and multiplexed surface plasmon resonance (SPR) biosensor for quantifying miRNAs without standard. We introduced the mass transport limitation (MTL) strategy for the absolute quantification of miRNAs. We first explore the mechanism of DNA capture and the condition for triggering MTL on the SPR biosensor. We demonstrated that probes of 22–25 nt in length with fewer influences of the secondary structure provide better triggering of MTL. For proof of concept studies, let-7a, miR-155 and miR-21 were selected as candidate targets. Based on the structure and kinetics analysis, we demonstrate the best capture probe efficiency, and this biosensor’s limit of detection (LOD) is 500 fM without any signal amplification. Furthermore, our biosensor achieves multiplex detection, which could detect three targets simultaneously. The quantitative results of miRNA indicated the great prospects of our biosensor in nucleic acid-related early diagnosis and biosensing.</p></div>","PeriodicalId":259,"journal":{"name":"Biosensors and Bioelectronics","volume":"244 ","pages":"Article 115776"},"PeriodicalIF":10.7000,"publicationDate":"2023-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosensors and Bioelectronics","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0956566323007182","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

As an important biomarker for diagnostics and therapeutics of various diseases, the low-cost, quantitative detection method of microRNAs (miRNAs) has recently caught broad attention. However, their small size and low abundance still derive challenges to quantification detection. In this study, we developed an ultrasensitive and multiplexed surface plasmon resonance (SPR) biosensor for quantifying miRNAs without standard. We introduced the mass transport limitation (MTL) strategy for the absolute quantification of miRNAs. We first explore the mechanism of DNA capture and the condition for triggering MTL on the SPR biosensor. We demonstrated that probes of 22–25 nt in length with fewer influences of the secondary structure provide better triggering of MTL. For proof of concept studies, let-7a, miR-155 and miR-21 were selected as candidate targets. Based on the structure and kinetics analysis, we demonstrate the best capture probe efficiency, and this biosensor’s limit of detection (LOD) is 500 fM without any signal amplification. Furthermore, our biosensor achieves multiplex detection, which could detect three targets simultaneously. The quantitative results of miRNA indicated the great prospects of our biosensor in nucleic acid-related early diagnosis and biosensing.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于层流SPR系统质量传输限制的microrna绝对定量。
作为多种疾病诊断和治疗的重要生物标志物,microRNAs (miRNAs)的低成本、定量检测方法近年来受到广泛关注。然而,它们的体积小,丰度低,仍然给定量检测带来挑战。在这项研究中,我们开发了一种超灵敏的多路表面等离子体共振(SPR)生物传感器,用于无标定量mirna。我们引入了mirna绝对定量的质量传输限制(MTL)策略。我们首先探索了DNA捕获的机制和触发SPR生物传感器MTL的条件。我们证明,22- 25nt长度的探针受二级结构影响较小,可以更好地触发MTL。为了验证概念研究,我们选择let-7a、miR-155和miR-21作为候选靶点。基于结构和动力学分析,我们证明了最佳的捕获探针效率,该生物传感器的检测极限(LOD)为500 fM,没有任何信号放大。此外,我们的生物传感器实现了多重检测,可以同时检测三个目标。miRNA的定量结果表明我们的生物传感器在核酸相关的早期诊断和生物传感方面具有广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Biosensors and Bioelectronics
Biosensors and Bioelectronics 工程技术-电化学
CiteScore
20.80
自引率
7.10%
发文量
1006
审稿时长
29 days
期刊介绍: Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.
期刊最新文献
Corrigendum to "Probiotic bacterial adsorption coupled with CRISPR/Cas12a system for mercury (II) ions detection" [Biosens. Bioelectron. 263 (2024) 116627]. Retraction notice to "A comprehensive study on transparent conducting oxides in compact microbial fuel cells: Integrated spectroscopic and electrochemical analyses for monitoring biofilm growth" [Biosens. Bioelectron. 250 (2024) 116067]. The value of electrochemical ratiometry in immunosensing: A systematic study. Conductive single enzyme nanocomposites prepared by in-situ growth of nanoscale polyaniline for high performance enzymatic bioelectrode. A skin-mountable flexible biosensor based on Cu-MOF/PEDOT composites for sweat ascorbic acid monitoring.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1