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连续均匀拉伸流中的单分子DNA嵌入

Single molecule DNA intercalation in continuous homogenous elongational flow.

作者信息

Griffis Joshua W, Safranovitch Mikhail M, Vyas Shilpi P, Gerrin Sean, Protozanova Ekaterina, Malkin Gene, Meltzer Robert H

机构信息

PathoGenetix, Woburn, MA 01801, USA.

出版信息

Lab Chip. 2014 Oct 7;14(19):3881-93. doi: 10.1039/c4lc00781f.

Abstract

Sequence-nonspecific staining of DNA with intercalating fluorophores is required for fluorescence-based length estimation of elongated DNA in optical mapping techniques. However, the observed length of a DNA molecule is affected by the relative concentrations of DNA and dye. In some applications, predetermination of DNA concentration may not be possible. Here we present a microfluidic approach in which individual DNA molecules are entrained by converging laminar sheath flows containing the intercalating dye PO-PRO-1. This provides uniform staining regardless of DNA concentration, and uniform elastic stretching of DNA in continuous elongational flow. On-chip intercalation provides a unique process for concentration-independent staining of long DNA fragments for the optical mapping method Genome Sequence Scanning (GSS), and normalizes intramolecular elasticity across a broad range of molecule lengths. These advances permit accurate mapping of observed molecules to sequence derived templates, thus improving detection of complex bacterial mixtures using GSS.

摘要

在光学图谱技术中,基于荧光的伸长DNA长度估计需要使用嵌入荧光团对DNA进行序列非特异性染色。然而,观察到的DNA分子长度受DNA和染料相对浓度的影响。在某些应用中,可能无法预先确定DNA浓度。在此,我们提出一种微流体方法,其中单个DNA分子通过汇聚的含有嵌入染料PO-PRO-1的层流鞘流被夹带。这提供了与DNA浓度无关的均匀染色,以及在连续伸长流中DNA的均匀弹性拉伸。芯片上的嵌入为光学图谱方法基因组序列扫描(GSS)中长DNA片段的浓度无关染色提供了独特的过程,并在广泛的分子长度范围内归一化分子内弹性。这些进展允许将观察到的分子准确映射到序列衍生模板,从而改进使用GSS对复杂细菌混合物的检测。

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