Optical detection of two-color-fluorophore barcode for nanopore DNA sensing

M. Zhang, I. Sychugov, T. Schmidt, J. Linnros
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Abstract

A simple schematic on parallel optical detection of two-fluorophore barcode for single-molecule nanopore sensing is presented. The chosen two fluorophores, ATTO-532 and DY-521-XL, emitting in well-separated spectrum range can be excited at the same wavelength. A beam splitter was employed to separate signals from the two fluorophores and guide them to the same CCD camera. Based on a conventional microscope, sources of background in the nanopore sensing system, including membranes, compounds in buffer solution, and a detection cell was characterized. By photoluminescence excitation measurements, it turned out that silicon membrane has a negligible photoluminescence under the examined excitation from 440 nm to 560 nm, in comparison with a silicon nitrite membrane. Further, background signals from the detection cell were suppressed. Brownian motion of 450 bps DNA labelled with single ATTO-532 or DY-521-XL was successfully recorded by our optical system.
用于纳米孔DNA传感的双色荧光条形码光学检测
提出了一种用于单分子纳米孔传感的双荧光团条形码平行光学检测的简单原理图。所选择的两个荧光团,ATTO-532和DY-521-XL,在分离良好的光谱范围内发射,可以在同一波长下被激发。采用分束器分离来自两个荧光团的信号,并将它们引导到同一个CCD相机。基于传统显微镜,表征了纳米孔传感系统的背景源,包括膜、缓冲溶液中的化合物和检测细胞。通过光致发光激发测量,发现与亚硝酸盐硅膜相比,硅膜在440 nm ~ 560 nm范围内的光致发光可以忽略不计。此外,来自检测单元的背景信号被抑制。我们的光学系统成功记录了单ATTO-532或DY-521-XL标记的450 bps DNA的布朗运动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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