Suppr超能文献

基于 DNA 功能化量子点的褶皱硅纳米粒子对膀胱癌 microRNAs 的无扩增分析。

Amplification-Free Analysis of Bladder Cancer MicroRNAs on Wrinkled Silica Nanoparticles with DNA-Functionalized Quantum Dots.

机构信息

Laboratory Medicine Center, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210011, China.

Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210011, China.

出版信息

Anal Chem. 2024 Mar 26;96(12):4860-4867. doi: 10.1021/acs.analchem.3c05204. Epub 2024 Mar 13.

Abstract

Bladder cancer (BC) occurrence and progression are accompanied by alterations in microRNAs (miRNAs) expression levels. Simultaneous detection of multiple miRNAs contributes to the accuracy and reliability of the BC diagnosis. In this work, wrinkled silica nanoparticles (WSNs) were applied as the microreactor for multiplex miRNAs analysis without enzymes or nucleic acid amplification. Conjugated on the surface of WSNs, the S9.6 antibody was adopted as the universal module for binding DNA/miRNA duplexes, regardless of their sequence. Furthermore, single-stranded DNA (ssDNA) was labeled with quantum dots (QDs) for identifying a given miRNA to form QDs-ssDNA/miRNA, which enabled the specific capture of the corresponding QDs on the wrinkled surface of WSNs. Based on the detection of fluorescence signals that were ultimately focused on WSNs, target miRNAs could be sensitively identified to a femtomolar level (5 fM) with a wide dynamic range of up to 6 orders of magnitude. The proposed strategy achieved high specificity to obviously distinguish single-base mutation sequences and possessed multiplex assay capability. Moreover, the assay exhibited excellent practicability in the multiplex detection of miRNAs in clinical serum specimens.

摘要

膀胱癌(BC)的发生和发展伴随着 microRNAs(miRNAs)表达水平的改变。同时检测多种 miRNAs 有助于提高 BC 诊断的准确性和可靠性。在这项工作中,我们应用皱状硅纳米粒子(WSNs)作为微反应器,无需酶或核酸扩增即可进行多重 miRNAs 分析。在 WSNs 表面结合的 S9.6 抗体被用作结合 DNA/miRNA 双链的通用模块,而与它们的序列无关。此外,单链 DNA(ssDNA)用量子点(QDs)标记以识别特定的 miRNA,形成 QDs-ssDNA/miRNA,这使得相应的 QDs 能够特异性地捕获到 WSNs 的皱状表面上。基于最终聚焦在 WSNs 上的荧光信号检测,可以以皮摩尔级(5 fM)的灵敏度敏感地识别靶 miRNAs,动态范围高达 6 个数量级。所提出的策略具有高特异性,能够明显区分单碱基突变序列,并具有多重分析能力。此外,该测定法在临床血清标本中 miRNA 的多重检测中表现出优异的实用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验