Nitta Takahiro, Hess Henry
Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
Nano Lett. 2005 Jul;5(7):1337-42. doi: 10.1021/nl050586t.
Active transport driven by molecular motors is a key technology for the continued miniaturization of lab-on-a-chip devices, because it is expected to enable nanofluidic devices with channel diameters of less than 1 microm and total channel lengths on the order of 1 mm. An important metric for a transport mechanism employed in an analytic device is dispersion, because it critically affects the sensitivity and resolution. Here, we investigate the mechanisms responsible for the dispersion of a swarm of "molecular shuttles", consisting of functionalized microtubules propelled by surface-adhered kinesin motor proteins. Using a simple model and measurements of the path persistence length, motional diffusion coefficient, and the distribution of average velocities, we found that, at the time scale relevant in the envisioned nanobiodevices, variations in the time-averaged velocities between shuttles will make a stronger contribution to the dispersion of the swarm than both the fluctuations around the time-averaged velocity of an individual shuttle and the fluctuations in path length due to wiggling within the channel. Overall, the dispersion of such molecular shuttles is comparable to the dispersion of a sample plug transported by electroosmotic flow.
由分子马达驱动的主动运输是实现芯片实验室设备持续小型化的关键技术,因为它有望实现通道直径小于1微米且总通道长度约为1毫米的纳米流体设备。分析设备中采用的运输机制的一个重要指标是扩散,因为它会严重影响灵敏度和分辨率。在此,我们研究了由表面附着的驱动蛋白马达蛋白推动的功能化微管组成的“分子穿梭体”群扩散的机制。通过使用一个简单的模型并测量路径持续长度、运动扩散系数和平均速度分布,我们发现,在设想的纳米生物设备相关的时间尺度上,穿梭体之间时间平均速度的变化对群体扩散的贡献将比单个穿梭体时间平均速度周围的波动以及通道内摆动导致的路径长度波动都更大。总体而言,这种分子穿梭体的扩散与电渗流运输的样品塞的扩散相当。