贻贝
水下
粘附
比索
部分
材料科学
纳米技术
化学
胶粘剂
生态学
立体化学
生物
地质学
有机化学
图层(电子)
海洋学
作者
Sohee Park,Sangsik Kim,YongSeok Jho,Dong Soo Hwang
出处
期刊:Langmuir
[American Chemical Society]
日期:2019-08-17
卷期号:35 (48): 16002-16012
被引量:47
标识
DOI:10.1021/acs.langmuir.9b01976
摘要
Mussel underwater adhesion is a model phenomenon important for the understanding of broader biological adhesion and the development of biomimetic wet adhesives. The catechol moiety of 3,4-dihydroxyphenyl-l-alanine (DOPA) is known to be actively involved in the mechanism of mussel underwater adhesion; however, other underwater adhesion mechanisms are also crucial. The surface forces apparatus (SFA) has often been used to explore the contributions of other mechanisms to mussel underwater adhesion; e.g., recent SFA-based nanomechanical studies have revealed that cation−π interactions, one of the strongest intermolecular interactions in water, are the pivotal interactions of adhesive proteins involved in underwater mussel adhesion. This mini-review surveys recent research on cation−π interactions and their contributions to strong mussel underwater adhesion, shedding light on some biological processes and facilitating the development of biomedical adhesives.
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