Adjacent cationic-aromatic sequences yield strong electrostatic adhesion of hydrogels in seawater.
Hailong FanJiahui WangZhen TaoJunchao HuangPing RaoTakayuki KurokawaJian Ping GongPublished in: Nature communications (2019)
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-π 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.
Keyphrases
- amino acid
- ionic liquid
- biofilm formation
- molecular dynamics simulations
- drug release
- drug delivery
- pseudomonas aeruginosa
- staphylococcus aureus
- candida albicans
- hyaluronic acid
- extracellular matrix
- escherichia coli
- molecularly imprinted
- genome wide
- tissue engineering
- genetic diversity
- wound healing
- cell migration
- high resolution
- single cell
- cell adhesion