Biomedical Engineering Department, Johns Hopkins University, Baltimore, Maryland 21218, USA.
J Am Chem Soc. 2011 May 11;133(18):6898-901. doi: 10.1021/ja200279y. Epub 2011 Apr 19.
Single-molecule free solution hydrodynamic separation (SML-FSHS) cohesively integrates cylindrical illumination confocal spectroscopy with free solution hydrodynamic separation. This technique enables single-molecule analysis of size separated DNA with 100% mass detection efficiency, high sizing resolution and wide dynamic range, surpassing the performance of single molecule capillary electrophoresis. Furthermore, SML-FSHS required only a bare fused silica microcapillary and simple pressure control rather than complex high voltage power supplies, sieving matrices, and wall coatings. The wide dynamic range and high sizing resolution of SML-FSHS was demonstrated by separating both large DNA (23 vs 27 kbp) and small DNA (100 vs 200 bp) under identical conditions. Separations were successfully performed with near zero sample consumption using as little as 5 pL of sample and 240 yoctomoles (∼150 molecules) of DNA. Quantitative accuracy was predominantly limited by molecular shot noise. Furthermore, the ability of this method to analyze of single molecule nanosensors was investigated. SML-FSHS was used to examine the thermodynamic equilibrium between stochastically open molecular beacon and target-bound molecular beacon in the detection of E. coli 16s rRNA targets.
单分子自由溶液流体动力学分离(SML-FSHS)将圆柱形照明共焦光谱学与自由溶液流体动力学分离紧密结合在一起。该技术能够对尺寸分离的 DNA 进行单分子分析,具有 100%的质量检测效率、高尺寸分辨率和宽动态范围,超过了单分子毛细管电泳的性能。此外,SML-FSHS 仅需要裸熔融二氧化硅微毛细管和简单的压力控制,而不需要复杂的高压电源、筛分基质和壁涂层。SML-FSHS 的宽动态范围和高尺寸分辨率通过在相同条件下分离大 DNA(23 与 27 kbp)和小 DNA(100 与 200 bp)来证明。使用仅 5 pL 的样品和 240 zeptomoles(约 150 个分子)的 DNA,就可以成功地进行接近零样品消耗的分离。定量准确性主要受分子射击噪声限制。此外,还研究了该方法分析单分子纳米传感器的能力。SML-FSHS 用于研究随机开放分子信标与目标结合的分子信标之间的热力学平衡,以检测大肠杆菌 16s rRNA 靶标。