• 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

通过 DNA 折纸基元上的单链置换反应对 microRNA 进行精确定量。

Accurate quantification of microRNA via single strand displacement reaction on DNA origami motif.

机构信息

Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, China.

出版信息

PLoS One. 2013 Aug 21;8(8):e69856. doi: 10.1371/journal.pone.0069856. eCollection 2013.

DOI:10.1371/journal.pone.0069856
PMID:23990889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3749204/
Abstract

DNA origami is an emerging technology that assembles hundreds of staple strands and one single-strand DNA into certain nanopattern. It has been widely used in various fields including detection of biological molecules such as DNA, RNA and proteins. MicroRNAs (miRNAs) play important roles in post-transcriptional gene repression as well as many other biological processes such as cell growth and differentiation. Alterations of miRNAs' expression contribute to many human diseases. However, it is still a challenge to quantitatively detect miRNAs by origami technology. In this study, we developed a novel approach based on streptavidin and quantum dots binding complex (STV-QDs) labeled single strand displacement reaction on DNA origami to quantitatively detect the concentration of miRNAs. We illustrated a linear relationship between the concentration of an exemplary miRNA as miRNA-133 and the STV-QDs hybridization efficiency; the results demonstrated that it is an accurate nano-scale miRNA quantifier motif. In addition, both symmetrical rectangular motif and asymmetrical China-map motif were tested. With significant linearity in both motifs, our experiments suggested that DNA Origami motif with arbitrary shape can be utilized in this method. Since this DNA origami-based method we developed owns the unique advantages of simple, time-and-material-saving, potentially multi-targets testing in one motif and relatively accurate for certain impurity samples as counted directly by atomic force microscopy rather than fluorescence signal detection, it may be widely used in quantification of miRNAs.

摘要

DNA 折纸术是一种新兴的技术,它可以将数百个订书钉和一条单链 DNA 组装成特定的纳米图案。它已广泛应用于各个领域,包括检测生物分子如 DNA、RNA 和蛋白质。MicroRNAs(miRNAs)在转录后基因沉默以及细胞生长和分化等许多其他生物学过程中发挥重要作用。miRNAs 表达的改变与许多人类疾病有关。然而,通过折纸技术定量检测 miRNAs 仍然是一个挑战。在本研究中,我们开发了一种基于链霉亲和素和量子点结合复合物(STV-QDs)标记单链置换反应的新型方法,用于定量检测 miRNAs 的浓度。我们说明了示例性 miRNA(miRNA-133)的浓度与 STV-QDs 杂交效率之间的线性关系;结果表明,它是一种准确的纳米级 miRNA 定量分子。此外,还测试了对称矩形图案和不对称中国地图图案。在这两种图案中都具有显著的线性关系,我们的实验表明,具有任意形状的 DNA 折纸图案都可以应用于这种方法。由于我们开发的这种基于 DNA 折纸术的方法具有独特的优势,例如简单、省时省力、在一个图案中可以进行多靶点测试,并且对于某些杂质样品相对准确,因为可以直接通过原子力显微镜而不是荧光信号检测进行计数,因此它可能广泛应用于 miRNAs 的定量检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/7bc668faef26/pone.0069856.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/fa0bf2b38755/pone.0069856.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/e9cfbf08fff2/pone.0069856.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/072fc1996d1a/pone.0069856.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/7bc668faef26/pone.0069856.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/fa0bf2b38755/pone.0069856.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/e9cfbf08fff2/pone.0069856.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/072fc1996d1a/pone.0069856.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9c/3749204/7bc668faef26/pone.0069856.g004.jpg

相似文献

1
Accurate quantification of microRNA via single strand displacement reaction on DNA origami motif.通过 DNA 折纸基元上的单链置换反应对 microRNA 进行精确定量。
PLoS One. 2013 Aug 21;8(8):e69856. doi: 10.1371/journal.pone.0069856. eCollection 2013.
2
[Single-molecule detection and characterization of DNA replication based on DNA origami].基于DNA折纸术的DNA复制的单分子检测与表征
Nan Fang Yi Ke Da Xue Xue Bao. 2014 Aug;34(9):1235-40.
3
DNA origami frame filled with two types of single-stranded tiles.DNA 折纸框架中填充有两种类型的单链瓦片。
Nanoscale. 2022 Apr 7;14(14):5340-5346. doi: 10.1039/d1nr05583f.
4
Highly selective and sensitive detection of miRNA based on toehold-mediated strand displacement reaction and DNA tetrahedron substrate.基于链置换反应和 DNA 四面体质子化底物的高选择性和高灵敏度 miRNA 检测。
Biosens Bioelectron. 2015 Sep 15;71:401-406. doi: 10.1016/j.bios.2015.04.067. Epub 2015 Apr 22.
5
Nanomechanical DNA origami 'single-molecule beacons' directly imaged by atomic force microscopy.原子力显微镜直接成像纳米机械 DNA 折纸“单分子信标”。
Nat Commun. 2011 Aug 23;2:449. doi: 10.1038/ncomms1452.
6
Nanomechanical molecular devices made of DNA origami.由 DNA 折纸术制成的纳米机械分子器件。
Acc Chem Res. 2014 Jun 17;47(6):1742-9. doi: 10.1021/ar400328v. Epub 2014 Apr 29.
7
Assembly of a DNA Origami Chinese Knot by Only 15% of the Staple Strands.仅用 15%的订书钉链组装 DNA 折纸中国结。
Chembiochem. 2020 Aug 3;21(15):2132-2136. doi: 10.1002/cbic.202000106. Epub 2020 Apr 9.
8
Stepwise and reversible nanopatterning of proteins on a DNA origami scaffold.在 DNA 折纸支架上逐步且可逆的蛋白质纳米图案化。
Chem Commun (Camb). 2010 Jul 28;46(28):5127-9. doi: 10.1039/c0cc00044b. Epub 2010 Jun 9.
9
Organizing DNA origami tiles into larger structures using preformed scaffold frames.使用预制支架框架将 DNA 折纸瓦片组织成更大的结构。
Nano Lett. 2011 Jul 13;11(7):2997-3002. doi: 10.1021/nl201603a. Epub 2011 Jun 23.
10
In situ monitoring of single molecule binding reactions with time-lapse atomic force microscopy on functionalized DNA origami.利用功能化 DNA 折纸术的延时原子力显微镜对单分子结合反应进行原位监测。
Nanoscale. 2011 Jun;3(6):2481-4. doi: 10.1039/c1nr10181a. Epub 2011 Apr 28.

引用本文的文献

1
Single-Molecule FRET: A Tool to Characterize DNA Nanostructures.单分子荧光共振能量转移:一种表征DNA纳米结构的工具。
Front Mol Biosci. 2022 Mar 7;9:835617. doi: 10.3389/fmolb.2022.835617. eCollection 2022.
2
DNA Origami-Enabled Biosensors.DNA 折纸术赋能的生物传感器。
Sensors (Basel). 2020 Dec 3;20(23):6899. doi: 10.3390/s20236899.
3
DNA nanotechnology approaches for microRNA detection and diagnosis.DNA 纳米技术在 microRNA 检测和诊断中的应用

本文引用的文献

1
DNA origami as a carrier for circumvention of drug resistance.DNA 折纸术作为克服耐药性的载体。
J Am Chem Soc. 2012 Aug 15;134(32):13396-403. doi: 10.1021/ja304263n. Epub 2012 Aug 1.
2
Rolling up gold nanoparticle-dressed DNA origami into three-dimensional plasmonic chiral nanostructures.将金纳米粒子包裹的 DNA 折纸滚成三维等离子体手性纳米结构。
J Am Chem Soc. 2012 Jan 11;134(1):146-9. doi: 10.1021/ja209861x. Epub 2011 Dec 13.
3
MiR-133a induces apoptosis through direct regulation of GSTP1 in bladder cancer cell lines.
Nucleic Acids Res. 2019 Nov 18;47(20):10489-10505. doi: 10.1093/nar/gkz580.
4
Duplex-Specific Nuclease-Amplified Detection of MicroRNA Using Compact Quantum Dot-DNA Conjugates.使用紧凑型量子点-DNA 偶联物的双链特异性核酸酶扩增检测 microRNA。
ACS Appl Mater Interfaces. 2018 Aug 29;10(34):28290-28300. doi: 10.1021/acsami.8b07250. Epub 2018 Aug 16.
5
A Novel Self-Assembling DNA Nano Chip for Rapid Detection of Human Papillomavirus Genes.一种用于快速检测人乳头瘤病毒基因的新型自组装DNA纳米芯片。
PLoS One. 2016 Oct 5;11(10):e0162975. doi: 10.1371/journal.pone.0162975. eCollection 2016.
6
Investigation of the Application of miR10b and miR135b in the Identification of Semen Stains.miR10b和miR135b在精液斑鉴定中的应用研究
PLoS One. 2015 Sep 10;10(9):e0137067. doi: 10.1371/journal.pone.0137067. eCollection 2015.
7
Molecular processes studied at a single-molecule level using DNA origami nanostructures and atomic force microscopy.利用DNA折纸纳米结构和原子力显微镜在单分子水平上研究的分子过程。
Molecules. 2014 Sep 3;19(9):13803-23. doi: 10.3390/molecules190913803.
miR-133a 通过直接调控 GSTP1 诱导膀胱癌细胞系凋亡。
Urol Oncol. 2013 Jan;31(1):115-23. doi: 10.1016/j.urolonc.2010.09.017. Epub 2011 Mar 10.
4
miR-145, miR-133a and miR-133b: Tumor-suppressive miRNAs target FSCN1 in esophageal squamous cell carcinoma.miR-145、miR-133a 和 miR-133b:抑癌 miRNAs 在食管鳞癌细胞中靶向 FSCN1。
Int J Cancer. 2010 Dec 15;127(12):2804-14. doi: 10.1002/ijc.25284.
5
Orthogonal protein decoration of DNA origami.DNA折纸的正交蛋白质修饰
Angew Chem Int Ed Engl. 2010 Dec 3;49(49):9378-83. doi: 10.1002/anie.201005931.
6
A DNA-Origami chip platform for label-free SNP genotyping using toehold-mediated strand displacement.一种用于无标记单核苷酸多态性基因分型的DNA折纸芯片平台,采用了引发链介导的链置换技术。
Small. 2010 Sep 6;6(17):1854-8. doi: 10.1002/smll.201000908.
7
Programmable periodicity of quantum dot arrays with DNA origami nanotubes.利用 DNA 折纸纳米管实现量子点阵列的可编程周期性。
Nano Lett. 2010 Sep 8;10(9):3367-72. doi: 10.1021/nl101079u.
8
Asymmetric DNA origami for spatially addressable and index-free solution-phase DNA chips.用于空间可寻址且无索引的溶液相DNA芯片的不对称DNA折纸术。
Adv Mater. 2010 Jun 25;22(24):2672-5. doi: 10.1002/adma.201000151.
9
IDH1 and IDH2 gene mutations identify novel molecular subsets within de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study.IDH1 和 IDH2 基因突变在新诊断的细胞遗传学正常急性髓系白血病中确定新的分子亚群:癌症和白血病组 B 研究。
J Clin Oncol. 2010 May 10;28(14):2348-55. doi: 10.1200/JCO.2009.27.3730. Epub 2010 Apr 5.
10
Single-molecule chemical reactions on DNA origami.DNA 折纸术上单分子化学反应。
Nat Nanotechnol. 2010 Mar;5(3):200-3. doi: 10.1038/nnano.2010.5. Epub 2010 Feb 28.