Pathogenetix, Inc., 12 Gill St., Suite 3150, Woburn, MA 01801, USA.
Lab Chip. 2013 Jan 21;13(2):240-51. doi: 10.1039/c2lc40943g. Epub 2012 Dec 3.
Genome Sequence Scanning (GSS) is a bacterial identification technology that detects sparse sequence-specific fluorescent tags on long DNA molecules linearized in a continuous-flow microfunnel. The efficiency and sensitivity of GSS depends on the detection throughput of well-stretched molecules. Previous studies have investigated the fundamental roles of elongational and shear flow on DNA stretching in continuous flow devices. Here, we present a novel compound funnel design that significantly improves effective molecule throughput over previously described devices. First, exploring the relationship between fluid strain rate and molecule tension allows for design of funnel geometries that accommodate high fluid velocities without compromising molecules due to overstretching under high tension. Second, a constant-strain detection channel is utilized to significantly reduce the number of molecules lost to further analysis due to shear-induced molecular tumbling and relaxation. Finally, application of the constant-strain detection channel allows for a priori prediction of spatial resolution bias due to accelerating flow. In all, the refined funnel geometries presented here yield over thirty-fold increase in effective molecule throughput due to increased fluid flow and improved retention of stretched molecules, compared to previously described devices.
基因组序列扫描(GSS)是一种细菌鉴定技术,它可以检测在线性连续流微流控装置中的长 DNA 分子上稀疏的序列特异性荧光标签。GSS 的效率和灵敏度取决于充分拉伸分子的检测通量。先前的研究已经研究了伸长和剪切流对连续流装置中 DNA 拉伸的基本作用。在这里,我们提出了一种新颖的复合漏斗设计,与之前描述的装置相比,显著提高了有效分子的吞吐量。首先,探索流体应变速率与分子张力之间的关系,设计出的漏斗几何形状能够适应高流速,而不会因高张力下的过度拉伸而损坏分子。其次,利用恒应变速率检测通道,可以大大减少由于剪切诱导的分子翻滚和松弛而导致的进一步分析中丢失的分子数量。最后,恒应变速率检测通道的应用可以预先预测由于加速流动而导致的空间分辨率偏差。总之,与之前描述的装置相比,这里提出的改进后的漏斗几何形状由于增加了流体流量和改善了拉伸分子的保留,使得有效分子的吞吐量增加了三十多倍。