Adjacent cationic-aromatic sequences yield strong electrostatic adhesion of hydrogels in seawater

被引:311
作者
Fan, Hailong [1 ,2 ]
Wang, Jiahui [3 ]
Tao, Zhen [3 ]
Huang, Junchao [2 ]
Rao, Ping [3 ]
Kurokawa, Takayuki [2 ,4 ]
Gong, Jian Ping [1 ,2 ,4 ]
机构
[1] Hokkaido Univ, Inst Chem React Design & Discovery WPIICReDD, Kita Ku, N21W10, Sapporo, Hokkaido 0010021, Japan
[2] Hokkaido Univ, Fac Adv Life Sci, Kita Ku, N21W11, Sapporo, Hokkaido 0010021, Japan
[3] Hokkaido Univ, Grad Sch Life Sci, Kita Ku, N21W11, Sapporo, Hokkaido 0010021, Japan
[4] Hokkaido Univ, Global Stn Soft Matter GI CoRE, Kita Ku, N21W11, Sapporo, Hokkaido 0010021, Japan
关键词
MUSSEL; POLYMERIZATION; COACERVATION; RESIDUES; BINDING;
D O I
10.1038/s41467-019-13171-9
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
Electrostatic interaction is strong but usually diminishes in high ionic-strength environments. Biosystems can use this interaction through adjacent cationic-aromatic amino acids sequence of proteins even in a saline medium. Application of such specific sequence to the development of cationic polymer materials adhesive to negatively charged surfaces in saline environments is challenging due to the difficulty in controlling the copolymer sequences. Here, we discover that copolymers with adjacent cation-aromatic sequences can be synthesized through cation-ic complex-aided free-radical polymerization. Sequence controlled hydrogels from diverse cation/aromatic monomers exhibit fast, strong but reversible adhesion to negatively charged surfaces in seawater. Aromatics on copolymers are found to enhance the electrostatic interactions of their adjacent cationic residues to the counter surfaces, even in a high ionic-strength medium that screens the electrostatic interaction for common polyelectrolytes. This work opens a pathway to develop adhesives using saline water.
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页数:8
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