Single molecule adsorption at compositionally patterned self-assembled monolayers on gold: Role of domain boundaries

被引:12
|
作者
Park, HY
Li, HW
Yeung, ES
Porter, MD [1 ]
机构
[1] Iowa State Univ, Ames Lab, USDOE, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[3] Iowa State Univ, Ames Lab, USDOE, Dept Chem, Ames, IA 50011 USA
[4] Iowa State Univ, Dept Biol & Chem Engn, Ames, IA 50011 USA
[5] Iowa State Univ, Inst Combinatorial Discovery, Ames, IA 50011 USA
关键词
D O I
10.1021/la053100x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper examines the single-molecule adsorption of YOYO-I-labeled lambda-DNA at compositionally patterned self-assembled monolayers (SAMs). The interactions of fluorescently labeled lambda-DNA molecule with the patterned SAMs, which are comprised of different functional groups (i.e., amine-, alcohol-, and acid-terminated thiolates), were monitored at optically transparent gold films using total internal reflection fluorescence microscopy. The role of solution pH, A-DNA concentration, and domain size was investigated. In addition to delineation of the relative adsorption strength as a function of terminal group identity (NH2 > COOH > OH), the potential importance of structural defects was also revealed. The latter result, found both at the disordered boundaries between domains and at adlayers in which structural order was affected by the length of the alkyl chain, points to the subtle but preferential adsorption of the "sticky ends" of lambda-DNA. These experiments also detected an intriguing dependence of adsorption with respect to domain size.
引用
收藏
页码:4244 / 4249
页数:6
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