Li Yiran, Wang Tiankuo, Xia Lei, Wang Lei, Qin Meng, Li Ying, Wang Wei, Cao Yi
Collaborative Innovation Center of Advanced Microstructures, National Laboratory of Solid State Microstructure, Department of Physics, Nanjing University, Nanjing 210093, P. R. China.
J Mater Chem B. 2017 Jun 21;5(23):4416-4420. doi: 10.1039/c7tb00131b. Epub 2017 Mar 10.
Using AFM based single-molecule force spectroscopy, we studied the synergy between Dopa and lysine for wet adhesion on titania (TiO) and mica surfaces. We found that the binding forces for lysine-Dopa dipeptides are significantly higher when the positive charge of lysine is unprotected on both surfaces. However, such a synergistic effect is absent when the sequence is reversed. We attribute such differential synergistic effects to their distinct structure for load distribution within the molecules, which may represent a general principle for synergistic strong adhesion.
我们使用基于原子力显微镜的单分子力谱技术,研究了多巴和赖氨酸在二氧化钛(TiO)和云母表面上的湿附着力协同作用。我们发现,当赖氨酸的正电荷在两个表面上均未被保护时,赖氨酸 - 多巴二肽的结合力显著更高。然而,当序列颠倒时,这种协同效应不存在。我们将这种不同的协同效应归因于它们在分子内负载分布的独特结构,这可能代表了协同强附着力的一般原理。