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基于一维微流控珠阵列的阳离子荧光聚合物核酸检测

Nucleic acids detection using cationic fluorescent polymer based on one-dimensional microfluidic beads array.

作者信息

Yang Xiaohai, Zhao Xiang, Zuo Xinbing, Wang Kemin, Wen Jianhui, Zhang He

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Engineering Center for Biomedicine, Institute of life science and Biotechnology, Changsha, PR China.

出版信息

Talanta. 2009 Jan 15;77(3):1027-31. doi: 10.1016/j.talanta.2008.08.001. Epub 2008 Aug 19.

Abstract

An assay for rapid and direct detection of DNA/mRNA using cationic fluorescent polymer based on one-dimensional microfluidic beads array (1-D chip) has been developed. The cationic water-soluble polythiophene derivatives can easily transduce hybridization events into measurable optical signal due to the conformational changes of the conjugated backbone, when mixed with single-stranded or double-stranded oligonucleotides. In this paper, the polymer was introduced into 1-D chip for fluorescence detection of nucleic acids, and demonstrated its capability on rapid detection of p53 complementary DNA (cDNA) with different concentration. Using this system, we have evaluated the mRNA expression changes of three tumor-associated genes (p53, c-myc and cyclin-d1) in human nasopharyngeal carcinoma CNE2 cell lines before and after 5-flouorouracil (5-FU) stimuli. These results were validated by the conventional reverse transcriptase-PCR. The most important advantage of this assay is not needed target or report labeling prior to hybridization, which makes the experiment process easy to handle and low-cost for multi-target measurement.

摘要

一种基于一维微流控珠阵列(一维芯片)使用阳离子荧光聚合物快速直接检测DNA/mRNA的分析方法已被开发出来。阳离子水溶性聚噻吩衍生物在与单链或双链寡核苷酸混合时,由于共轭主链的构象变化,能够轻松地将杂交事件转化为可测量的光学信号。在本文中,该聚合物被引入一维芯片用于核酸的荧光检测,并展示了其对不同浓度的p53互补DNA(cDNA)进行快速检测的能力。使用该系统,我们评估了人鼻咽癌CNE2细胞系在5-氟尿嘧啶(5-FU)刺激前后三种肿瘤相关基因(p53、c-myc和细胞周期蛋白d1)的mRNA表达变化。这些结果通过传统的逆转录聚合酶链反应得到了验证。该分析方法最重要的优点是在杂交前不需要对靶标或报告分子进行标记,这使得实验过程易于操作且多靶标测量成本低。

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