Raichur A M, Vörös J, Textor M, Fery A
Max Planck Institute for Colloids and Interfaces, Golm 14476 Germany.
Biomacromolecules. 2006 Aug;7(8):2331-6. doi: 10.1021/bm060270v.
Adhesion of PAH/PSS and PDADMAC/PSS capsules through electrostatic and specific interactions has been investigated using reflective interference contrast microscopy (RICM). Adhesion of capsules via electrostatic interactions was found to be spontaneous and strong. Capsules functionalized with poly(l-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) did not exhibit significant adhesion (as determined by the adhesion area) to streptavidin-coated substrates, whereas capsules functionalized with biotinylated PLL-g-PEG showed a significantly larger adhesion area. Using continuum mechanical models, the total adhesion energies for these cases were calculated and were found to correspond to several tens of individual biotin-streptavidin pairs. The application of specific interactions such as the biotin-streptavidin system for controlled capsule adhesion has been demonstrated in this study.
已使用反射干涉对比显微镜(RICM)研究了聚对苯二甲酸乙二酯/聚苯乙烯磺酸钠(PAH/PSS)和聚二烯丙基二甲基氯化铵/聚苯乙烯磺酸钠(PDADMAC/PSS)胶囊通过静电和特异性相互作用的粘附情况。发现通过静电相互作用的胶囊粘附是自发且强烈的。用聚(L-赖氨酸)-接枝-聚(乙二醇)(PLL-g-PEG)功能化的胶囊对链霉亲和素包被的底物没有表现出明显的粘附(由粘附面积确定),而用生物素化的PLL-g-PEG功能化的胶囊显示出明显更大的粘附面积。使用连续介质力学模型计算了这些情况下的总粘附能,发现其对应于几十对单个生物素-链霉亲和素对。本研究证明了特异性相互作用如生物素-链霉亲和素系统在控制胶囊粘附中的应用。