A versatile method for generating single DNA molecule patterns: Through the combination of directed capillary assembly and (micro/nano) contact printing

被引:13
作者
Cerf, Aline [1 ,2 ]
Dollat, Xavier [1 ,2 ]
Chalmeau, Jerome [1 ,2 ,3 ]
Coutable, Angelique [4 ,5 ]
Vieu, Christophe [1 ,2 ]
机构
[1] CNRS, LAAS, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, INSA, INP,ISAE,LAAS, F-31077 Toulouse, France
[3] Univ Minnesota, Dept Phys, Minneapolis, MN 55416 USA
[4] Univ Toulouse, INSA, UPS, INP,LISBP, F-31077 Toulouse, France
[5] CNRS, UMR5504, INRA, Ingn Syst Biol & Proc UMR792, F-31400 Toulouse, France
关键词
ATOMIC-FORCE MICROSCOPY; STRETCHED DNA; CHIPS; NANOWIRES; ARRAYS; CONSTRUCTION; MANIPULATION; LITHOGRAPHY; POLYMER; SURFACE;
D O I
10.1557/jmr.2010.12
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
One of the challenges in the development of molecular scale devices is the integration of nano-objects or molecules onto desired locations on a surface. This integration comprises their accurate positioning, their alignment, and the preservation of their functionality. Here, we proved how capillary assembly in combination with soft lithography can be used to perform DNA molecular combing to generate chips of isolated DNA strands for genetic analysis and diagnosis. The assembly of DNA molecules is achieved on a topologically micropatterned polydimethylsiloxane stamp inducing almost simultaneously the trapping and stretching of single molecules. The DNA molecules are then transferred onto aminopropyltriethoxysilane-coated surfaces. In fact, this technique offers the possibility to tightly control the experimental parameters to direct the assembly process. This technique does not induce a selection in size of the objects, therefore it can handle complex solutions of long (tens of kbp) but also shorter (a few thousands of bp) molecules directly in solution to allow the construction of future one-dimensional nanoscale building templates.
引用
收藏
页码:336 / 346
页数:11
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