Raynal Bertrand D E, Hardingham Timothy E, Thornton David J, Sheehan John K
Wellcome Trust Centre for Cell-Matrix Research, School of Biological Sciences, University of Manchester, 2.205 Stopford Building, Manchester M13 9PT, UK.
Biochem J. 2002 Mar 1;362(Pt 2):289-96. doi: 10.1042/0264-6021:3620289.
We have developed a new approach to study the molecular organization of salivary mucus and salivary mucins using confocal fluorescence recovery after photobleaching (confocal-FRAP). MUC5B mucin, its reduced subunit and T-domains were prepared from saliva and fluorescently labelled. The translational self-diffusion coefficients were determined up to 3.6 mg/ml by confocal-FRAP. The results suggest that, in solutions of purified MUC5B mucin, at concentrations at which the hydrodynamic domains overlap, the intermolecular interactions are predominantly due to dynamic entanglements, and there was no evidence of specific self-association of MUC5B mucin, or of its subunits, or T-domains. The analysis of the salivary mucus gel also showed no specific interactions with the purified MUC5B components, but it was much less permeable than expected from its MUC5B content. The saliva was completely permeable to microspheres of 207 nm diameter, but showed size-dependent effects on the diffusion of larger microspheres (499 nm and 711 nm diameter). From these analyses the salivary mucus was shown to be both permeable and dynamic, and with the characteristics of a semi-dilute transient network at physiological concentration. Comparison of the results from saliva and purified MUC5B mucin solutions showed that the network properties of saliva were equivalent to a solution of purified MUC5B mucin of 10-20 times higher concentration. This showed that saliva has additional structure and organization not present in the purified MUC5B mucin and suggests there are other interactions and/or components within saliva that combine with MUC5B to produce its complete properties.
我们开发了一种新方法,利用共聚焦光漂白后荧光恢复技术(共聚焦-FRAP)来研究唾液黏液和唾液黏蛋白的分子组织。从唾液中制备了MUC5B黏蛋白、其降解亚基和T结构域,并进行了荧光标记。通过共聚焦-FRAP测定了浓度高达3.6 mg/ml时的平移自扩散系数。结果表明,在纯化的MUC5B黏蛋白溶液中,当流体动力学结构域重叠时,分子间相互作用主要是由于动态缠结,没有证据表明MUC5B黏蛋白及其亚基或T结构域存在特异性自缔合。对唾液黏液凝胶的分析也表明,它与纯化的MUC5B成分没有特异性相互作用,但它的渗透性比根据其MUC5B含量预期的要低得多。唾液对直径为207 nm的微球完全可渗透,但对较大微球(直径499 nm和711 nm)的扩散表现出尺寸依赖性影响。通过这些分析表明,唾液黏液既具有渗透性又具有动态性,在生理浓度下具有半稀释瞬态网络的特征。唾液和纯化的MUC5B黏蛋白溶液结果的比较表明,唾液的网络特性相当于浓度高10-20倍的纯化MUC5B黏蛋白溶液。这表明唾液具有纯化的MUC5B黏蛋白中不存在的额外结构和组织,表明唾液中存在其他与MUC5B结合以产生其完整特性的相互作用和/或成分。