Han J, Craighead H G
School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.
Science. 2000 May 12;288(5468):1026-9. doi: 10.1126/science.288.5468.1026.
A nanofluidic channel device, consisting of many entropic traps, was designed and fabricated for the separation of long DNA molecules. The channel comprises narrow constrictions and wider regions that cause size-dependent trapping of DNA at the onset of a constriction. This process creates electrophoretic mobility differences, thus enabling efficient separation without the use of a gel matrix or pulsed electric fields. Samples of long DNA molecules (5000 to approximately 160,000 base pairs) were efficiently separated into bands in 15-millimeter-long channels. Multiple-channel devices operating in parallel were demonstrated. The efficiency, compactness, and ease of fabrication of the device suggest the possibility of more practical integrated DNA analysis systems.
一种由许多熵阱组成的纳米流体通道装置被设计并制造出来,用于分离长链DNA分子。该通道包括狭窄的收缩区和较宽的区域,这些区域会在收缩开始时导致DNA因尺寸不同而被捕获。这个过程产生了电泳迁移率差异,从而无需使用凝胶基质或脉冲电场就能实现高效分离。长链DNA分子(5000至约160,000个碱基对)的样本在15毫米长的通道中被高效分离成条带。展示了并行运行的多通道装置。该装置的高效性、紧凑性和易于制造表明了构建更实用的集成DNA分析系统的可能性。