Cabodi Mario, Turner Stephen W P, Craighead Harold G
School of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA.
Anal Chem. 2002 Oct 15;74(20):5169-74. doi: 10.1021/ac025879a.
A novel technique that can rapidly separate long-strand polymers according to length is presented. The separation mechanism is mediated by a confinement-induced entropic force at the abrupt interface between regions of vastly different configuration entropy. To demonstrate this technique, DNA molecules were partially inserted into a dense array of nanopillars (an entropically unfavorable region) using a pulsed electric field and allowed to relax to their natural state by removal of the field. Molecules of dissimilar lengths (T2 and T7 coliphage DNA) were inserted into this region in such a way that shorter molecules were fully inserted in this region, while longer molecules remained partially across the interface. The longer T2 molecules were observed to recoil entirely out of the pillar array, leaving the shorter T7 molecules inserted, and effecting separation of the two species in a single step. To show how this method can be used for separation of unknown samples, the inserting electric field was pulsed for progressively longer times, allowing passage of progressively longer molecules and producing the equivalent of a conventional electropherogram. The effects limiting resolution in this device are discussed, and the expected separating power of a multistage device is reported. The extracted resolution and running separation time compare favorably with current conventional separation techniques.
本文提出了一种能够根据长度快速分离长链聚合物的新技术。分离机制是由在构型熵差异极大的区域之间的突变界面处的限域诱导熵力介导的。为了演示该技术,使用脉冲电场将DNA分子部分插入密集的纳米柱阵列(一个熵不利区域),然后通过去除电场使其松弛至自然状态。将不同长度的分子(T2和T7噬菌体DNA)以这样的方式插入该区域:较短的分子完全插入该区域,而较长的分子部分留在界面处。观察到较长的T2分子完全从柱阵列中反冲出来,而较短的T7分子仍留在插入状态,从而在一步中实现了两种分子的分离。为了展示该方法如何用于分离未知样品,对插入电场进行了逐渐延长时间的脉冲处理,允许逐渐更长的分子通过,并产生了相当于传统电泳图的结果。讨论了限制该装置分辨率的因素,并报告了多级装置的预期分离能力。提取的分辨率和运行分离时间与当前的传统分离技术相比具有优势。