Combinatorial-Entropy-Driven Aggregation in DNA-Grafted Nanoparticles

被引:18
作者
Sciortino, Francesco [1 ]
Zhang, Yugang [2 ]
Gang, Oleg [2 ,3 ,4 ]
Kumar, Sanat K. [3 ]
机构
[1] Sapienza Univ Roma, Dept Phys, I-00185 Rome, Italy
[2] Brookhaven Natl Labs, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[4] Columbia Univ, Dept Appl Phys & Appl Math, New York, NY 10027 USA
关键词
DNA; grafted colloids; entropic effects; crystallization; simulation; POLYMERS; MODEL; CRYSTALLIZATION; NETWORKS;
D O I
10.1021/acsnano.9b10123
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We use computer simulations and experiments to study the interactions between nanoparticles (NPs) grafted with self-complementary DNA strands. Each strand ends with a sticky palindromic single-stranded sequence, allowing it to associate equally favorably with strands grafted on the same particle or on different NPs. Surprisingly we find an attractive interaction between a pair of NPs, and we demonstrate that at low temperature it arises purely from a combinatorial-entropy contribution. We evaluate theoretically and verify numerically this entropic contribution originating from the number of distinct bonding patterns associated with intra- and interparticle binding. This entropic attraction becomes more favorable with decreasing inter-NP distance because more sticky ends can participate in making this choice.
引用
收藏
页码:5628 / 5635
页数:8
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