School of Mechanical Engineering, and ‡Weldon School of Biomedical Engineering, Purdue University , West Lafayette, Indiana 47906, United States.
Anal Chem. 2017 Dec 19;89(24):13334-13341. doi: 10.1021/acs.analchem.7b03513. Epub 2017 Dec 6.
Analytical characterization of DNA microviscosity provides critical biophysical insights into nuclear crowding, nucleic acid based pharmaceutical development, and nucleic acid based biosensor device design. However, most viscosity characterization methods require large sample volumes and destructive testing. In contrast, particle diffusometry permits in situ analysis of DNA microviscosity with short measurement times (8 s) using small volumes (<3 μL) which are compatible with DNA preparatory procedures. This unconventional biosensing approach involves measuring the change in sample viscosity using image processing and correlation-based algorithms. Particle diffusometry requires only a fluorescence microscope equipped with a charge-coupled device (CCD) camera and is a nondestructive measurement method. We use particle diffusometry to characterize the effect of DNA topology, length, and concentration on solution viscosity. In addition, we use particle diffusometry to detect the amplification of DNA from Staphylococcus aureus and Klebsiella pneumoniae, two pathogens commonly related to neonatal sepsis. Successful characterization of pathogen amplification with particle diffusometry provides a new opportunity to apply viscosity characterization toward downstream applications in nucleic acid based pathogen detection.
DNA 微粘度的分析特性为核拥挤、基于核酸的药物开发以及基于核酸的生物传感器设备设计提供了关键的生物物理见解。然而,大多数粘度特性化方法需要大的样品体积和破坏性测试。相比之下,粒子扩散测量法允许使用小体积(<3 μL)和短测量时间(8 s)原位分析 DNA 微粘度,这与 DNA 预备程序兼容。这种非常规的生物传感方法涉及使用图像处理和基于相关的算法来测量样品粘度的变化。粒子扩散测量法仅需要配备电荷耦合器件(CCD)相机的荧光显微镜,并且是一种非破坏性的测量方法。我们使用粒子扩散测量法来表征 DNA 拓扑结构、长度和浓度对溶液粘度的影响。此外,我们还使用粒子扩散测量法来检测金黄色葡萄球菌和肺炎克雷伯菌(两种与新生儿败血症有关的常见病原体)的 DNA 扩增。粒子扩散测量法成功地对病原体扩增进行了特征描述,为将粘度特征化应用于基于核酸的病原体检测的下游应用提供了新的机会。