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本文引用的文献

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Micro total analysis systems: latest achievements.微全分析系统:最新成果
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2
Charge-coupled device operated in a time-delayed integration mode as an approach to high-throughput flow-based single molecule analysis.电荷耦合器件以延时积分模式运行,作为一种基于高通量流式单分子分析的方法。
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用于监测生化反应的高通量单分子检测

High throughput single molecule detection for monitoring biochemical reactions.

作者信息

Okagbare Paul I, Soper Steven A

机构信息

Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Analyst. 2009 Jan;134(1):97-106. doi: 10.1039/b816383a. Epub 2008 Nov 24.

DOI:10.1039/b816383a
PMID:19082181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2664543/
Abstract

The design, performance and application of a novel optical system for high throughput single molecule detection (SMD) configured in a continuous flow format using microfluidics is reported. The system consisted of a microfabricated polymer-based multi-channel fluidic network situated within the optical path of a laser source (lambda(ex) = 660 nm) with photon transduction accomplished using an electron-multiplying charge coupled device (EMCCD) operated in a frame transfer mode that allowed tracking single molecules as they passed through a large field-of-view (FoV) illumination zone. The microfluidic device consisted of 30 microchannels possessing dimensions of 30 microm (width) x 20 microm (depth) with a 25 microm pitch. Individual molecules were electrokinetically driven through the fluidic network and excited within the wide-field illumination area with the resulting fluorescence collected via an objective and imaged onto the EMCCD camera. The detection system demonstrated sufficient sensitivity to detect single DNA molecules labeled with a fluorescent tag (AlexaFluor 660) identified through their characteristic emission wavelength and the burst of photons produced during their transit through the excitation volume. In its present configuration and fluidic architecture, the sample processing throughput was approximately 4.02 x 10(5) molecules s(-1), but could be increased dramatically through the use of narrower channels and a smaller pitch. The system was further evaluated using a single molecule-based fluorescence quenching assay for measuring the population differences between duplexed and single-stranded DNA molecules as a function of temperature for determining the duplex melting temperature, T(m).

摘要

报道了一种新型光学系统的设计、性能及应用,该系统采用微流控技术以连续流动形式配置,用于高通量单分子检测(SMD)。该系统由一个基于聚合物微加工的多通道流体网络组成,该网络位于激光源(激发波长λ(ex)=660 nm)的光路中,利用在帧转移模式下工作的电子倍增电荷耦合器件(EMCCD)实现光子转换,从而能够跟踪单分子通过大视场(FoV)照明区的过程。微流控装置由30个微通道组成,通道尺寸为30微米(宽)×20微米(深),间距为25微米。单个分子通过电动驱动穿过流体网络,并在宽场照明区域内被激发,产生的荧光通过物镜收集并成像到EMCCD相机上。该检测系统具有足够的灵敏度,能够检测用荧光标签(AlexaFluor 660)标记的单个DNA分子,通过其特征发射波长以及在其穿过激发体积期间产生的光子爆发来识别。在其当前配置和流体结构下,样品处理通量约为4.02×10⁵个分子·秒⁻¹,但通过使用更窄的通道和更小的间距可显著提高通量。该系统还通过基于单分子的荧光猝灭测定法进行了进一步评估,以测量双链和单链DNA分子群体差异随温度的变化,从而确定双链解链温度T(m)。