Li Yiran, Liu Huanyu, Wang Tiankuo, Qin Meng, Cao Yi, Wang Wei
National Laboratory of Solid State Microstructure, Department of Physics, Nanjing University, 22 Hankou Road, Nanjing, Jiangsu, 210093, China.
Chemphyschem. 2017 Jun 2;18(11):1466-1469. doi: 10.1002/cphc.201600374. Epub 2016 Jun 7.
Inspired by marine mussel adhesive systems, numerous 3,4-dihydroxyphenylalanine (DOPA)-containing surface coating materials have been recently designed. It is well known that DOPA has a strong adhesion ability to different kinds of wet surfaces. However, the molecular mechanism of DOPA adhesion remains elusive. Recent biophysical studies of DOPA adhesion by both surface force apparatus (SFA) and atomic force microscopy (AFM) suggest that DOPA can bind to a wide range of surfaces exhibiting diverse chemical properties through different binding mechanisms. Here, using AFM-based single-molecule force spectroscopy, we show that even for chemically well-defined crystal surfaces, DOPA can bind to them by multiple binding modes. The binding forces between DOPA and different rutile TiO surfaces can vary within a broad range from 40-800 pN at a pulling speed of 1000 nm s and are largely dependent on the surface properties. Our findings indicate that the local chemical environment can greatly affect DOPA adhesion, and that single-molecule force spectroscopy is a unique tool to reveal the heterogeneity of DOPA adhesion to the same surface.
受海洋贻贝粘附系统的启发,最近人们设计了许多含3,4-二羟基苯丙氨酸(DOPA)的表面涂层材料。众所周知,DOPA对不同种类的潮湿表面具有很强的粘附能力。然而,DOPA粘附的分子机制仍然难以捉摸。最近通过表面力仪(SFA)和原子力显微镜(AFM)对DOPA粘附进行的生物物理研究表明,DOPA可以通过不同的结合机制与具有不同化学性质的广泛表面结合。在这里,我们使用基于AFM的单分子力谱表明,即使对于化学性质明确的晶体表面,DOPA也可以通过多种结合模式与它们结合。在1000 nm s的拉伸速度下,DOPA与不同金红石TiO表面之间的结合力可以在40 - 800 pN的宽范围内变化,并且在很大程度上取决于表面性质。我们的研究结果表明,局部化学环境可以极大地影响DOPA的粘附,并且单分子力谱是揭示DOPA对同一表面粘附异质性的独特工具。