Organization of 'nanocrystal molecules' using DNA

被引:2511
作者
Alivisatos, AP [1 ]
Johnsson, KP [1 ]
Peng, XG [1 ]
Wilson, TE [1 ]
Loweth, CJ [1 ]
Bruchez, MP [1 ]
Schultz, PG [1 ]
机构
[1] UNIV CALIF BERKELEY,LAWRENCE BERKELEY NATL LAB,INST MOL DESIGN,BERKELEY,CA 94701
关键词
D O I
10.1038/382609a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
PATTERNING matter on the nanometre scale is an important objective of current materials chemistry and physics. It is driven by both the need to further miniaturize electronic components and the fact that at the nanometre scale, materials properties are strongly size-dependent and thus can be tuned sensitively(1). In nanoscale crystals, quantum size effects and the large number of surface atoms influence the, chemical, electronic, magnetic and optical behaviour(2-4). 'Top-down' (for example, lithographic) methods for nanoscale manipulation reach only to the upper end of the nanometre regime(5); but whereas 'bottom-up' wet chemical techniques allow for the preparation of monodisperse, defect-free crystallites just 1-10 nm in size(6-10), ways to control the structure of nanocrystal assemblies are scarce. Here we describe a strategy for the synthesis of 'nanocrystal molecules', in which discrete numbers of gold nanocrystals are organized into spatially defined structures based on Watson-Crick base-pairing interactions. We attach single-stranded DNA oligonucleotides of defined length and sequence to individual nanocrystals, and these assemble into dimers and trimers on addition of a complementary single-stranded DNA template, We anticipate that this approach should allow the construction of more complex two- and three-dimensional assemblies.
引用
收藏
页码:609 / 611
页数:3
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