Transient self-organisation of DNA coated colloids directed by enzymatic reactions

被引:16
作者
Dehne, H. [1 ]
Reitenbach, A. [1 ]
Bausch, A. R. [1 ]
机构
[1] Tech Univ Munich, Lehrstuhl Zellbiophys, James Franck Str 1, D-85748 Garching, Germany
关键词
PARTICLES; CLUSTERS; GOLD;
D O I
10.1038/s41598-019-43720-7
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
Dynamic self-organisation far from equilibrium is a key concept towards building autonomously acting materials. Here, we report the coupling of an antagonistic enzymatic reaction of RNA polymerisation and degradation to the aggregation of micron sized DNA coated colloids into fractal structures. A transient colloidal aggregation process is controlled by competing reactions of RNA synthesis of linker strands by a RNA polymerase and their degradation by a ribonuclease. By limiting the energy supply (NTP) of the enzymatic reactions, colloidal clusters form and subsequently disintegrate without the need of external stimuli. Here, the autonomous colloidal aggregation and disintegration can be modulated in terms of lifetime and cluster size. By restricting the enzyme activity locally, a directed spatial propagation of a colloidal aggregation and disintegration front is realised.
引用
收藏
页数:9
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