Sequential self-assembly of DNA functionalized droplets

被引:58
作者
Zhang, Yin [1 ]
McMullen, Angus [1 ]
Pontani, Lea-Laetitia [1 ,3 ]
He, Xiaojin [1 ]
Sha, Ruojie [2 ]
Seeman, Nadrian C. [2 ]
Brujic, Jasna [1 ]
Chaikin, Paul M. [1 ]
机构
[1] NYU, Phys Dept, Ctr Soft Matter Res, 4 Washington Pl, New York, NY 10003 USA
[2] NYU, Chem Dept, 100 Washington Sq East, New York, NY 10003 USA
[3] Univ Paris 06, Ctr Natl Rech Sci, Inst NanoSci Paris, UMR 7588, 4 Pl Jussieu, Paris, France
基金
美国国家科学基金会;
关键词
STRAND DISPLACEMENT; COLLOIDAL CRYSTALS; EXCHANGE MECHANISM; BIOPHYSICS; EMULSIONS; KINETICS; VALENCE; FORCES;
D O I
10.1038/s41467-017-00070-0
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
Complex structures and devices, both natural and manmade, are often constructed sequentially. From crystallization to embryogenesis, a nucleus or seed is formed and built upon. Sequential assembly allows for initiation, signaling, and logical programming, which are necessary for making enclosed, hierarchical structures. Although biology relies on such schemes, they have not been available in materials science. Here, we demonstrate programmed sequential self-assembly of DNA functionalized emulsions. The droplets are initially inert because the grafted DNA strands are pre-hybridized in pairs. Active strands on initiator droplets then displace one of the paired strands and thus release its complement, which in turn activates the next droplet in the sequence, akin to living polymerization. Our strategy provides time and logic control during the self-assembly process, and offers a new perspective on the synthesis of materials.
引用
收藏
页数:7
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