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基于悬臂式生物传感器的产毒蓝藻铜绿微囊藻 16S rRNA 检测方法。

A cantilever biosensor-based assay for toxin-producing cyanobacteria Microcystis aeruginosa using 16S rRNA.

机构信息

Department of Chemical and Biological Engineering, Drexel University , Philadelphia, Pennsylvania 19104, United States.

出版信息

Environ Sci Technol. 2013;47(21):12333-41. doi: 10.1021/es402925k. Epub 2013 Oct 10.

Abstract

Monitoring of cyanotoxins in source waters is currently done through toxin-targeting assays which suffer from low sensitivity due to poor antibody avidity. We present a biosensor-based method as an alternative for detecting toxin-producing cyanobacteria M. aeruginosa via species-selective region of 16S rRNA at concentrations as low as 50 cells/mL, and over a five-log dynamic range. The cantilever biosensor was immobilized with a 27-base DNA strand that is complementary to the target variable region of 16S rRNA of M. aeruginosa. The cantilever sensor detects mass-changes through shifts in its resonant frequency. Increase in the biosensor's effective mass, caused by hybridization of target strand with the biosensor-immobilized complementary strand, showed consistent and proportional frequency shift to M. aeruginosa concentrations. The sensor hybridization response was verified in situ by two techniques: (a) presence of duplex DNA structure postdetection via fluorescence measurements, and (b) secondary hybridization of nanogold-labeled DNA strands to the captured 16S rRNA strands. The biosensor-based assay, conducted in a flow format (∼ 0.5 mL/min), is relatively short, and requires a postextraction analysis time of less than two hours. The two-step detection protocol (primary and secondary hybridization) is less prone to false negatives, and the technique as a whole can potentially provide an early warning for toxin presence in source waters.

摘要

目前,对水源中蓝藻毒素的监测是通过针对毒素的检测方法进行的,但由于抗体亲和力差,这些方法的灵敏度较低。我们提出了一种基于生物传感器的方法,用于通过 16S rRNA 的种特异性区域来检测产毒蓝藻铜绿微囊藻,其检测浓度低至 50 个细胞/mL,动态范围为五个对数级。悬臂式生物传感器通过与铜绿微囊藻 16S rRNA 目标可变区互补的 27 个碱基 DNA 链固定化。悬臂传感器通过其共振频率的变化来检测质量变化。由于目标链与生物传感器固定化的互补链杂交,增加了生物传感器的有效质量,从而导致生物传感器的共振频率发生一致的、成比例的偏移,与铜绿微囊藻的浓度相对应。通过两种技术原位验证了传感器的杂交反应:(a)通过荧光测量检测到双链 DNA 结构的存在,以及(b)纳米金标记的 DNA 链与捕获的 16S rRNA 链的二次杂交。基于生物传感器的检测方法以流动形式(约 0.5 mL/min)进行,相对较短,并且提取后的分析时间不到两个小时。两步检测方案(初级和次级杂交)不太容易出现假阴性,并且整个技术有可能为水源中存在毒素提供早期预警。

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