Academic Unit of Ophthalmology, Bristol Eye Hospital, University of Bristol, Bristol, United Kingdom.
Biophys J. 2012 Jan 4;102(1):176-84. doi: 10.1016/j.bpj.2011.08.058. Epub 2012 Jan 3.
Moist mucosal epithelial interfaces that are exposed to external environments are dominated by sugar epitopes, some of which (e.g., sialic acids) are involved in host defense. In this study, we determined the abundance and distribution of two sialic acids to assess differences in their availability to an exogenous probe in isolated mucins and mucous gels. We used atomic force microscopy to obtain force maps of human preocular mucous and purified ocular mucins by probing and locating the interactions between tip-tethered lectins Maackia amurensis and Sambucus nigra and their respective receptors, α-2,3 and α-2,6 N-acetylneuraminic (sialic) acids. The rupture force distributions were not affected by neighboring sugar-bearing molecules. Energy contours for both lectin-sugar bonds were fitted to a two-barrier model, suggesting a conformational change before dissociation. In contrast to data from purified mucin molecules, the preocular gels presented numerous large clusters (19,000 ± 4000 nm(2)) of α-2,6 sialic acids, but very few small clusters (2000 ± 500 nm(2)) of α-2,3 epitopes. This indicates that mucins, which are rich in α-2,3 sialic acids, are only partially exposed at the surface of the mucous gel. Microorganisms that recognize α-2,3 sialic acids will encounter only isolated ligands, and the adhesion of other microorganisms will be enhanced by large islands of neighboring α-2,6 sialic acids. We have unveiled an additional level of mucosal surface heterogeneity, specifically in the distribution of pro- and antiadhesive sialic acids that protect underlying epithelia from viruses and bacteria.
暴露于外部环境的湿润黏膜上皮界面主要由糖表位组成,其中一些(例如唾液酸)参与宿主防御。在这项研究中,我们确定了两种唾液酸的丰度和分布,以评估它们在分离的粘蛋白和粘液凝胶中对外源探针的可及性差异。我们使用原子力显微镜通过探测和定位尖端连接的凝集素 Maackia amurensis 和 Sambucus nigra 及其各自的受体α-2,3 和 α-2,6 N-乙酰神经氨酸(唾液酸)与人类眼前粘液和纯化的眼粘液之间的相互作用,获得了人眼前粘液和纯化的眼粘液的力图谱。断裂力分布不受相邻带糖分子的影响。两种凝集素-糖键的能量轮廓均拟合到双势垒模型,表明在解离之前存在构象变化。与来自纯化粘蛋白分子的数据相比,眼前凝胶呈现出许多大的α-2,6 唾液酸簇(19,000 ± 4000nm²),但α-2,3 表位的小簇(2000 ± 500nm²)却很少。这表明富含α-2,3 唾液酸的粘蛋白仅部分暴露于粘液凝胶的表面。识别α-2,3 唾液酸的微生物将仅遇到分离的配体,而相邻α-2,6 唾液酸的大岛将增强其他微生物的粘附。我们揭示了粘膜表面异质性的另一个层次,特别是在保护上皮免受病毒和细菌侵害的亲水性和抗粘性唾液酸的分布上。