Howard P. Isermann Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
Langmuir. 2010 Aug 17;26(16):13393-8. doi: 10.1021/la101679n.
This manuscript describes the influence of chain length on the diffusion and electrophoresis of single stranded DNA (ssDNA) adsorbed on heterogeneous cationic supported lipid bilayers. These studies are motivated by the increasing interest in developing novel strategies for the separation of DNA. We studied ssDNA molecules with the number of bases (N) varying from 21 to 84. Fluorescence recovery after photobleaching (FRAP) studies revealed that the diffusivity (D) of adsorbed ssDNA varied with N as D approximately N(-1), similar to a trend previously observed for the diffusion of double stranded DNA on homogeneous supported lipid bilayers. In contrast, the electrophoretic mobility of the adsorbed ssDNA in the presence of an applied tangential electric field was independent of N. Our studies indicated that the motion of ssDNA in the presence of an applied electric field was primarily due to electrophoresis and was not influenced significantly by electro-osmotic flow. Our results also suggest that the use of asymmetric diffusion barriers or other tunable obstacles may assist DNA separation on supported lipid bilayers.
本文描述了链长对吸附在异质阳离子支撑脂质双层上的单链 DNA(ssDNA)扩散和电泳的影响。这些研究的动机是为了开发分离 DNA 的新策略。我们研究了碱基数量(N)从 21 到 84 的 ssDNA 分子。荧光漂白后荧光恢复(FRAP)研究表明,吸附的 ssDNA 的扩散系数(D)随 N 的变化而变化,类似于先前在均相支撑脂质双层上观察到的双链 DNA 扩散的趋势。相比之下,在施加切向电场的情况下,吸附的 ssDNA 的电泳迁移率与 N 无关。我们的研究表明,在施加电场的情况下,ssDNA 的运动主要是由于电泳,而电渗流的影响不大。我们的结果还表明,使用不对称扩散屏障或其他可调障碍可能有助于在支撑脂质双层上进行 DNA 分离。