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腔内 DNA 熔解分析与光流控激光。

Intracavity DNA melting analysis with optofluidic lasers.

机构信息

Department of Biomedical Engineering, University of Michigan, 1101 Beal Avenue, Ann Arbor, Michigan 48109, United States.

出版信息

Anal Chem. 2012 Nov 6;84(21):9558-63. doi: 10.1021/ac302416g. Epub 2012 Oct 9.

DOI:10.1021/ac302416g
PMID:23017119
Abstract

DNA melting analysis holds great promise for simple and fast DNA sequence discrimination. However, conventional fluorescence-based methods suffer from a small differential signal and demanding melting curve analysis, both of which make it difficult to distinguish the target DNA from the mismatched one. Herein, we propose and demonstrate a highly specific intracavity DNA melting analysis scheme utilizing an optofluidic laser. The laser optically amplifies the small yet intrinsic thermal dynamic difference between the target and the single-base-mismatched DNA, resulting in a differential signal that is orders of magnitude greater than with fluorescence-based methods. In particular, the existence of a phase transition between the stimulated laser emission and fluorescence (i.e., spontaneous emission) enables accurate determination of the DNA transition temperature difference. Furthermore, the high differential signal in the intracavity detection allows for scanning of the laser excitation at a fixed temperature to distinguish two DNA sequences, which provides another means for rapid DNA analysis. In this paper, we first theoretically investigate DNA melting analysis using an optofluidic laser and then experimentally explore this scheme with a high-quality optofluidic ring resonator. Distinction of two DNA sequences of up to 100 bases long is demonstrated. The intracavity detection developed here will lead to novel optofluidic devices that enable rapid and simple analysis of DNAs with very long sequences.

摘要

DNA 熔解分析在简单、快速的 DNA 序列鉴别方面具有广阔的应用前景。然而,传统的荧光基方法存在差分信号小和熔解曲线分析要求高的问题,这使得难以将目标 DNA 与错配的 DNA 区分开来。在此,我们提出并展示了一种基于光流体激光的高特异性腔内 DNA 熔解分析方案。该激光光学放大了目标 DNA 和单碱基错配 DNA 之间微小但固有的热动力学差异,产生了比荧光基方法大几个数量级的差分信号。特别是,受激激光发射与荧光(即自发发射)之间的相变能够准确确定 DNA 相变温度差。此外,腔内检测的高差分信号允许在固定温度下扫描激光激发,以区分两种 DNA 序列,这为快速 DNA 分析提供了另一种手段。在本文中,我们首先从理论上研究了基于光流体激光的 DNA 熔解分析,然后使用高质量的光流体环形谐振器对该方案进行了实验探索。实验证明,该方案可以区分长达 100 个碱基的两种 DNA 序列。这里开发的腔内检测将导致新型的光流体器件的出现,从而实现对具有非常长序列的 DNA 的快速、简单分析。

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