• 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

荧光编码 DNA 纳米结构探针系统,通过原位筛选双重细胞内 microRNA 特征实现肿瘤异质性的区分。

Fluorescence-coded DNA Nanostructure Probe System to Enable Discrimination of Tumor Heterogeneity via a Screening of Dual Intracellular microRNA Signatures in situ.

机构信息

School of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea.

School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea.

出版信息

Sci Rep. 2017 Oct 18;7(1):13499. doi: 10.1038/s41598-017-13456-3.

DOI:10.1038/s41598-017-13456-3
PMID:29044199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5647416/
Abstract

Since the delivery kinetics of different cell types are different, the signal from the target cell is greatly affected by the noise signal of the diagnostic system. This is a major obstacle hindering the practical application of intracellular diagnostic systems, such as tumor heterogeneity. To address these issues, here we present a microRNA detection platform using fluorescence-encoded nanostructured DNA-based probes. The nanostructured DNA was designed to include molecular beacons for detecting cytosolic microRNA as well as additional fluorophores. When the intracellular diagnostic system is delivered, fluorescence signals are generated by the molecular beacons, depending on the concentration of the target microRNA. The fluorescence signals are then normalized to the intensity of the additional fluorophore. Through this simple calculation, the concentration of intracellular microRNA can be determined without interference from the diagnosis system itself. And also it enabled discrimination of microRNA expression heterogeneity in five different breast cancer cell lines.

摘要

由于不同细胞类型的释放动力学不同,因此目标细胞的信号会受到诊断系统噪声信号的很大影响。这是阻碍细胞内诊断系统(如肿瘤异质性)实际应用的主要障碍。为了解决这些问题,我们在这里提出了一种使用荧光编码纳米结构 DNA 探针进行 microRNA 检测的平台。纳米结构 DNA 被设计为包含分子信标,用于检测细胞质 microRNA 以及其他荧光团。当递送到细胞内诊断系统时,分子信标根据目标 microRNA 的浓度产生荧光信号。然后将荧光信号归一化为附加荧光团的强度。通过这种简单的计算,可以确定细胞内 microRNA 的浓度,而不会受到诊断系统本身的干扰。并且还能够区分五种不同乳腺癌细胞系中 microRNA 表达的异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/ff4057ad4860/41598_2017_13456_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/f9f98a4cd3ad/41598_2017_13456_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/f639e32f85f3/41598_2017_13456_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/9660f8c3a97b/41598_2017_13456_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/bd369ba3bd2a/41598_2017_13456_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/8573f775ad9e/41598_2017_13456_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/a5b8eb0471fa/41598_2017_13456_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/ff4057ad4860/41598_2017_13456_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/f9f98a4cd3ad/41598_2017_13456_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/f639e32f85f3/41598_2017_13456_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/9660f8c3a97b/41598_2017_13456_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/bd369ba3bd2a/41598_2017_13456_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/8573f775ad9e/41598_2017_13456_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/a5b8eb0471fa/41598_2017_13456_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6f/5647416/ff4057ad4860/41598_2017_13456_Fig7_HTML.jpg

相似文献

1
Fluorescence-coded DNA Nanostructure Probe System to Enable Discrimination of Tumor Heterogeneity via a Screening of Dual Intracellular microRNA Signatures in situ.荧光编码 DNA 纳米结构探针系统,通过原位筛选双重细胞内 microRNA 特征实现肿瘤异质性的区分。
Sci Rep. 2017 Oct 18;7(1):13499. doi: 10.1038/s41598-017-13456-3.
2
Intracellular MicroRNA Imaging with MoS-Supported Nonenzymatic Catassembly of DNA Hairpins.基于 MoS 支撑的非酶 DNA 发夹自组装的细胞内 MicroRNA 成像。
ACS Appl Mater Interfaces. 2019 Jun 12;11(23):20725-20733. doi: 10.1021/acsami.9b04883. Epub 2019 May 30.
3
Nanolantern-Based DNA Probe and Signal Amplifier for Tumor-Related Biomarker Detection in Living Cells.基于纳米灯笼的 DNA 探针和信号放大器用于活细胞中肿瘤相关生物标志物的检测。
Anal Chem. 2019 Oct 15;91(20):13165-13173. doi: 10.1021/acs.analchem.9b03453. Epub 2019 Sep 24.
4
Dual amplification ratiometric biosensor based on a DNA tetrahedron nanostructure and hybridization chain reaction for the ultrasensitive detection of microRNA-133a.基于 DNA 四面体纳米结构和杂交链式反应的双扩增比率型生物传感器用于超灵敏检测 microRNA-133a。
Chem Commun (Camb). 2019 Sep 24;55(77):11551-11554. doi: 10.1039/c9cc05592d.
5
High-Discrimination Factor Nanosensor Based on Tetrahedral DNA Nanostructures and Gold Nanoparticles for Detection of MiRNA-21 in Live Cells.基于四面体 DNA 纳米结构和金纳米粒子的高分辨因子纳米传感器用于活细胞中 miRNA-21 的检测。
Theranostics. 2018 Mar 27;8(9):2424-2434. doi: 10.7150/thno.23852. eCollection 2018.
6
The construction of a novel nucleic acids detection microplatform based on the NSET for one-step detecting TK1-DNA and microRNA-21.基于 NSET 的新型核酸检测微平台的构建,用于一步法检测 TK1-DNA 和 microRNA-21。
Biosens Bioelectron. 2017 Nov 15;97:26-33. doi: 10.1016/j.bios.2017.05.039. Epub 2017 May 23.
7
Multicolor-Encoded Reconfigurable DNA Nanostructures Enable Multiplexed Sensing of Intracellular MicroRNAs in Living Cells.多色编码可重构 DNA 纳米结构可实现活细胞内多种细胞内 microRNAs 的多重检测。
ACS Appl Mater Interfaces. 2016 Jun 1;8(21):13303-8. doi: 10.1021/acsami.6b03165. Epub 2016 May 19.
8
Hybridization chain reaction amplification of microRNA detection with a tetrahedral DNA nanostructure-based electrochemical biosensor.基于四面体 DNA 纳米结构的电化学生物传感器杂交链式反应扩增 miRNA 检测。
Anal Chem. 2014 Feb 18;86(4):2124-30. doi: 10.1021/ac4037262. Epub 2014 Feb 4.
9
Specific and Direct Amplified Detection of MicroRNA with MicroRNA:Argonaute-2 Cleavage (miRACle) Beacons.利用 miRACle 探针特异性和直接扩增检测 microRNA:Argonaute-2 切割
Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13704-13708. doi: 10.1002/anie.201707366. Epub 2017 Sep 27.
10
Bioinspired Framework Nucleic Acid Capture Sensitively and Rapidly Resolving MicroRNAs Biomarkers in Living Cells.仿生框架核酸灵敏快速捕获活细胞中的 microRNAs 生物标志物。
Anal Chem. 2020 Mar 17;92(6):4411-4418. doi: 10.1021/acs.analchem.9b05304. Epub 2020 Feb 26.

引用本文的文献

1
Nano-Biosensors for mRNA-Based Cell Sorting Using Intracellular Markers at the Early Stage of Cell Reprogramming.用于在细胞重编程早期使用细胞内标志物进行基于mRNA的细胞分选的纳米生物传感器。
Adv Funct Mater. 2025 Jan 2;35(1). doi: 10.1002/adfm.202410910. Epub 2024 Nov 30.
2
Hybrid material of structural DNA with inorganic compound: synthesis, applications, and perspective.结构DNA与无机化合物的杂化材料:合成、应用及展望
Nano Converg. 2020 Jan 6;7(1):2. doi: 10.1186/s40580-019-0211-4.
3
Static DNA Nanostructures For Cancer Theranostics: Recent Progress In Design And Applications.

本文引用的文献

1
Towards clinically translatable nanodiagnostics.迈向临床可转化的纳米诊断技术。
Nat Rev Mater. 2017 May;2(5). doi: 10.1038/natrevmats.2017.14. Epub 2017 May 3.
2
DNA Tetrahedron Delivery Enhances Doxorubicin-Induced Apoptosis of HT-29 Colon Cancer Cells.DNA四面体递送增强阿霉素诱导的HT-29结肠癌细胞凋亡。
Nanoscale Res Lett. 2017 Aug 15;12(1):495. doi: 10.1186/s11671-017-2272-9.
3
Protecting microRNAs from RNase degradation with steric DNA nanostructures.利用空间位阻DNA纳米结构保护微小RNA免受核糖核酸酶降解。
用于癌症诊疗的静态DNA纳米结构:设计与应用的最新进展
Nanotechnol Sci Appl. 2019 Oct 15;12:25-46. doi: 10.2147/NSA.S227193. eCollection 2019.
4
A Low-Cost Time-Correlated Single Photon Counting Portable DNA Analyzer.一种低成本的时间相关单光子计数便携式 DNA 分析仪。
Sensors (Basel). 2019 Jun 26;19(13):2838. doi: 10.3390/s19132838.
Chem Sci. 2017 Feb 1;8(2):1062-1067. doi: 10.1039/c6sc01829g. Epub 2016 Sep 14.
4
Nondestructive nanostraw intracellular sampling for longitudinal cell monitoring.用于纵向细胞监测的非破坏性纳米吸管细胞内采样。
Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):E1866-E1874. doi: 10.1073/pnas.1615375114. Epub 2017 Feb 21.
5
Advances in the clinical translation of nanotechnology.纳米技术临床转化的进展
Curr Opin Biotechnol. 2017 Aug;46:66-73. doi: 10.1016/j.copbio.2017.01.002. Epub 2017 Feb 7.
6
Precision diagnostics: moving towards protein biomarker signatures of clinical utility in cancer.精准诊断:向癌症临床应用的蛋白质生物标志物特征迈进。
Nat Rev Cancer. 2017 Mar;17(3):199-204. doi: 10.1038/nrc.2016.153. Epub 2017 Feb 3.
7
Self-Assembly of Hierarchical DNA Nanotube Architectures with Well-Defined Geometries.具有明确定位几何形状的分级 DNA 纳米管结构的自组装。
ACS Nano. 2017 Feb 28;11(2):1927-1936. doi: 10.1021/acsnano.6b08008. Epub 2017 Jan 19.
8
New Advances in Nanotechnology-Based Diagnosis and Therapeutics for Breast Cancer: An Assessment of Active-Targeting Inorganic Nanoplatforms.基于纳米技术的乳腺癌诊断与治疗新进展:主动靶向无机纳米平台评估
Bioconjug Chem. 2017 Jan 18;28(1):135-152. doi: 10.1021/acs.bioconjchem.6b00591. Epub 2017 Jan 4.
9
Controlling DNA-nanoparticle serum interactions.控制DNA纳米颗粒与血清的相互作用。
Proc Natl Acad Sci U S A. 2016 Nov 29;113(48):13600-13605. doi: 10.1073/pnas.1610028113. Epub 2016 Nov 16.
10
Cancer nanomedicine: progress, challenges and opportunities.癌症纳米医学:进展、挑战与机遇。
Nat Rev Cancer. 2017 Jan;17(1):20-37. doi: 10.1038/nrc.2016.108. Epub 2016 Nov 11.