• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于杂交链式反应的相敏表面等离子体共振生物传感放大。

Biosensing Amplification by Hybridization Chain Reaction on Phase-Sensitive Surface Plasmon Resonance.

机构信息

Graduate Institute of Bioelectronics and Bioinformatics, National Taiwan University, Taipei 106, Taiwan.

Department of Medical Biotechnology and Laboratory Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.

出版信息

Biosensors (Basel). 2021 Mar 6;11(3):75. doi: 10.3390/bios11030075.

DOI:10.3390/bios11030075
PMID:33800935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7998988/
Abstract

Surface Plasmon Resonance (SPR) is widely used in biological and chemical sensing with fascinating properties. However, the application of SPR to detect trace targets is hampered by non-specific binding and poor signal. A variety of approaches for amplification have been explored to overcome this deficiency including DNA aptamers as versatile target detection tools. Hybridization chain reaction (HCR) is a high-efficiency enzyme-free DNA amplification method operated at room temperature, in which two stable species of DNA hairpins coexist in solution until the introduction of the initiator strand triggers a cascade of hybridization events. At an optimal salt condition, as the concentrations of H1 and H2 increased, the HCR signals were enhanced, leading to signal amplification reaching up to 6.5-fold of the detection measure at 30 min. This feature enables DNA to act as an amplifying transducer for biosensing applications to provide an enzyme-free alternative that can easily detect complex DNA sequences. Improvement of more diverse recognition events can be achieved by integrating HCR with a phase-sensitive SPR (pSPR)-tested aptamer stimulus. This work seeks to establish pSPR aptamer system for highly informative sensing by means of an amplification HCR. Thus, combining pSPR and HCR technologies provide an expandable platform for sensitive biosensing.

摘要

表面等离子体共振(SPR)具有迷人的特性,被广泛应用于生物和化学传感。然而,SPR 应用于痕量目标检测受到非特异性结合和信号差的限制。为了克服这一缺陷,已经探索了各种放大方法,包括 DNA 适体作为多功能的目标检测工具。杂交链式反应(HCR)是一种在室温下进行的高效无酶 DNA 扩增方法,其中两种稳定的 DNA 发夹在溶液中共存,直到引入引发链触发级联杂交事件。在最佳盐条件下,随着 H1 和 H2 浓度的增加,HCR 信号增强,导致信号放大达到 30 分钟时检测测量值的 6.5 倍。这一特性使 DNA 能够作为生物传感应用的放大换能器,提供一种无酶的替代方案,能够轻松检测复杂的 DNA 序列。通过将 HCR 与相位敏感 SPR(pSPR)-测试适体刺激相结合,可以实现更多样化识别事件的改进。本工作旨在通过放大 HCR 建立 pSPR 适体系统,实现高信息量传感。因此,结合 pSPR 和 HCR 技术为敏感的生物传感提供了一个可扩展的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/cc42fcd62298/biosensors-11-00075-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/d0dc38724490/biosensors-11-00075-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/6154655b4888/biosensors-11-00075-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/98f11dbd787c/biosensors-11-00075-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/862219aec21a/biosensors-11-00075-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/cc42fcd62298/biosensors-11-00075-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/d0dc38724490/biosensors-11-00075-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/6154655b4888/biosensors-11-00075-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/98f11dbd787c/biosensors-11-00075-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/862219aec21a/biosensors-11-00075-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae4/7998988/cc42fcd62298/biosensors-11-00075-g005.jpg

相似文献

1
Biosensing Amplification by Hybridization Chain Reaction on Phase-Sensitive Surface Plasmon Resonance.基于杂交链式反应的相敏表面等离子体共振生物传感放大。
Biosensors (Basel). 2021 Mar 6;11(3):75. doi: 10.3390/bios11030075.
2
An enzyme-free surface plasmon resonance biosensing strategy for detection of DNA and small molecule based on nonlinear hybridization chain reaction.一种基于非线性杂交链式反应的无需酶的表面等离子体共振生物传感策略,用于检测 DNA 和小分子。
Biosens Bioelectron. 2017 Jan 15;87:345-351. doi: 10.1016/j.bios.2016.08.077. Epub 2016 Aug 24.
3
Target-triggering multiple-cycle amplification strategy for ultrasensitive detection of adenosine based on surface plasma resonance techniques.基于表面等离子体共振技术的用于超灵敏检测腺苷的靶触发多循环扩增策略
Anal Chem. 2015 Jan 20;87(2):929-36. doi: 10.1021/ac503016f. Epub 2014 Dec 24.
4
Surface plasmon resonance biosensor for sensitive detection of microRNA and cancer cell using multiple signal amplification strategy.基于表面等离子体共振生物传感器的 miRNA 和癌细胞灵敏检测的多重信号放大策略
Biosens Bioelectron. 2017 Jan 15;87:433-438. doi: 10.1016/j.bios.2016.08.090. Epub 2016 Aug 27.
5
Establishment of a universal and sensitive plasmonic biosensor platform based on the hybridization chain reaction (HCR) amplification induced by a triple-helix molecular switch.基于三螺旋分子开关诱导的杂交链式反应(HCR)扩增的通用、灵敏等离子体生物传感器平台的建立。
Analyst. 2020 Jun 7;145(11):3864-3870. doi: 10.1039/d0an00249f. Epub 2020 Apr 9.
6
Microfluidic electrophoretic non-enzymatic kanamycin assay making use of a stirring bar functionalized with gold-labeled aptamer, of a fluorescent DNA probe, and of signal amplification via hybridization chain reaction.基于金标记适体功能化搅拌棒、荧光 DNA 探针,以及杂交链式反应信号放大的微流控电泳无酶卡那霉素检测法。
Mikrochim Acta. 2018 Feb 17;185(3):181. doi: 10.1007/s00604-017-2635-z.
7
Highly efficient fluorescence sensing of kanamycin using Endo IV-powered DNA walker and hybridization chain reaction amplification.基于内切酶 IV 驱动的 DNA walker 和杂交链式反应扩增的庆大霉素高灵敏荧光传感检测。
Mikrochim Acta. 2020 Mar 2;187(3):193. doi: 10.1007/s00604-020-4167-1.
8
Highly sensitive detection of Salmonella based on dual-functional HCR-mediated multivalent aptamer and amplification-free CRISPR/Cas12a system.基于双功能HCR介导的多价适体和无扩增CRISPR/Cas12a系统的沙门氏菌高灵敏度检测
Anal Chim Acta. 2023 Dec 15;1284:341998. doi: 10.1016/j.aca.2023.341998. Epub 2023 Nov 3.
9
Hairpin assembly circuit-based fluorescence cooperative amplification strategy for enzyme-free and label-free detection of small molecule.基于发夹组装的荧光协同放大策略用于酶和标记物自由的小分子检测。
Talanta. 2015 Oct 1;143:101-106. doi: 10.1016/j.talanta.2015.05.072. Epub 2015 May 27.
10
Enzyme-free surface plasmon resonance aptasensor for amplified detection of adenosine via target-triggering strand displacement cycle and Au nanoparticles.无酶表面等离子体共振适体传感器,通过靶标触发链置换循环和金纳米粒子进行扩增检测腺苷。
Anal Chim Acta. 2015 Apr 29;871:28-34. doi: 10.1016/j.aca.2015.02.028. Epub 2015 Feb 12.

引用本文的文献

1
Advances in Nanoplasmonic Biosensors: Optimizing Performance for Exosome Detection Applications.纳米等离子体生物传感器的进展:优化外泌体检测应用的性能。
Biosensors (Basel). 2024 Jun 14;14(6):307. doi: 10.3390/bios14060307.
2
Boosting the detection performance of severe acute respiratory syndrome coronavirus 2 test through a sensitive optical biosensor with new superior antibody.通过具有新型优质抗体的灵敏光学生物传感器提高严重急性呼吸综合征冠状病毒2检测性能。
Bioeng Transl Med. 2022 Sep 16;8(5):e10410. doi: 10.1002/btm2.10410.
3
Molecularly Imprinting-Aptamer Techniques and Their Applications in Molecular Recognition.

本文引用的文献

1
Point-of-care diagnostics for infectious diseases: From methods to devices.传染病的即时诊断:从方法到设备。
Nano Today. 2021 Apr;37:101092. doi: 10.1016/j.nantod.2021.101092. Epub 2021 Feb 6.
2
Nano-size dependence in the adsorption by the SARS-CoV-2 spike protein over gold colloid.新冠病毒刺突蛋白对金胶体吸附的纳米尺寸依赖性
Colloids Surf A Physicochem Eng Asp. 2021 Apr 20;615:126275. doi: 10.1016/j.colsurfa.2021.126275. Epub 2021 Feb 4.
3
Epigallocatechin-3-gallate, an active ingredient of Traditional Chinese Medicines, inhibits the 3CLpro activity of SARS-CoV-2.
分子印迹-适体技术及其在分子识别中的应用。
Biosensors (Basel). 2022 Jul 29;12(8):576. doi: 10.3390/bios12080576.
4
Loop-mediated isothermal amplification-based electrochemical sensor for detecting SARS-CoV-2 in wastewater samples.基于环介导等温扩增的电化学传感器用于检测废水样本中的新型冠状病毒2019(SARS-CoV-2)
J Environ Chem Eng. 2022 Jun;10(3):107488. doi: 10.1016/j.jece.2022.107488. Epub 2022 Feb 28.
5
A Simple Phase-Sensitive Surface Plasmon Resonance Sensor Based on Simultaneous Polarization Measurement Strategy.基于同时偏振测量策略的简单相敏表面等离子体共振传感器。
Sensors (Basel). 2021 Nov 16;21(22):7615. doi: 10.3390/s21227615.
6
Recent Advancements in Aptamer-Based Surface Plasmon Resonance Biosensing Strategies.基于适体的表面等离子体共振生物传感策略的最新进展。
Biosensors (Basel). 2021 Jul 10;11(7):233. doi: 10.3390/bios11070233.
表没食子儿茶素没食子酸酯,一种中药的有效成分,抑制 SARS-CoV-2 的 3CLpro 活性。
Int J Biol Macromol. 2021 Apr 15;176:1-12. doi: 10.1016/j.ijbiomac.2021.02.012. Epub 2021 Feb 4.
4
Spectroscopic investigation on the affinity of SARS-CoV-2 spike protein to gold nano-particles.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白与金纳米颗粒亲和力的光谱研究。
Colloid Interface Sci Commun. 2021 Jan;40:100356. doi: 10.1016/j.colcom.2020.100356. Epub 2020 Dec 26.
5
Biosensors as a future diagnostic approach for COVID-19.生物传感器作为 COVID-19 的未来诊断方法。
Life Sci. 2021 May 15;273:119117. doi: 10.1016/j.lfs.2021.119117. Epub 2021 Jan 26.
6
Potential of surface plasmon resonance biosensors in cancer detection.表面等离子体共振生物传感器在癌症检测中的应用潜力。
J Pharm Biomed Anal. 2021 Feb 5;194:113802. doi: 10.1016/j.jpba.2020.113802. Epub 2020 Nov 27.
7
Challenging TaqMan probe-based real-time PCR and loop-mediated isothermal amplification (LAMP): the two sensitive molecular techniques for the detection of toxoplasmosis, a potentially dangerous opportunistic infection in immunocompromised patients.TaqMan 探针实时 PCR 和环介导等温扩增(LAMP)技术的挑战:两种用于检测弓形虫病的敏感分子技术,弓形虫病是免疫功能低下患者潜在的危险机会性感染。
Arch Microbiol. 2020 Sep;202(7):1881-1888. doi: 10.1007/s00203-020-01903-1. Epub 2020 May 24.
8
Hybridization Chain Reactions Targeting the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).杂交链式反应靶向严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)。
Int J Mol Sci. 2020 May 1;21(9):3216. doi: 10.3390/ijms21093216.
9
Performance of the Alethia CMV Assay for Detection of Cytomegalovirus by Use of Neonatal Saliva Swabs.使用新生儿唾液拭子的Alethia巨细胞病毒检测法检测巨细胞病毒的性能
J Clin Microbiol. 2020 Mar 25;58(4). doi: 10.1128/JCM.01951-19.
10
Utilizing multiplex fluor LAMPs to illuminate multiple gene expressions in situ.利用多重荧光 LAMPs 原位检测多个基因的表达。
PLoS One. 2019 Oct 4;14(10):e0223333. doi: 10.1371/journal.pone.0223333. eCollection 2019.