Almond Andrew
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, United Kingdom.
Carbohydr Res. 2005 Apr 11;340(5):907-20. doi: 10.1016/j.carres.2005.01.014.
Complex carbohydrates are implicated in many important biological processes, and have a strong interaction with water. This close interplay with molecular water through multiple hydroxyls may be an integral part of their emergent structure and dynamics, as selected during evolution. Using molecular dynamics simulations with explicit water the interactions at the linkages within a variety of oligosaccharides are investigated and contrasted, in order to establish correlations between linkage orientation, sugar epimerization, and water interaction. In particular, interactions at alpha linkages, and between mannose and glucose residues, that are common in oligosaccharides are considered. Sugars joined by alpha linkages at the 2-, 3-, and 6-position were found to interact via a combination of weak hydrogen-bonds and water-bridges, which is dependent on the epimerization state of the sugars. Due to their three-dimensional structure, they are also likely to interact with noncontiguous sugar residues in an oligosaccharide, which can lead to ordered structures through the exclusion of water. On the other hand, beta linkages (to 3- and 4-position) maintain strong hydrogen-bonds, have a limited ability to be involved in water-bridges, and predominantly interact with the directly attached sugars. Therefore, sequences of alpha-linked sugars form compact, branched structures that have conformational flexibility, and beta linkages form extended, relatively rigid structures, suitable for structural molecules, and at the termini of protein bound oligosaccharides. These results provide further tentative ties between chemical structure, water interactions, and the emergent form and function of specific sugars and linkages in oligosaccharides.
复合碳水化合物参与许多重要的生物过程,并与水有强烈的相互作用。通过多个羟基与分子水的这种紧密相互作用可能是其在进化过程中所选择的新兴结构和动力学的一个组成部分。使用含有显式水的分子动力学模拟,研究并对比了多种寡糖内连接键处的相互作用,以建立连接键取向、糖差向异构化和水相互作用之间的相关性。特别考虑了寡糖中常见的α连接键处以及甘露糖和葡萄糖残基之间的相互作用。发现在2-、3-和6-位通过α连接键连接的糖通过弱氢键和水桥的组合相互作用,这取决于糖的差向异构化状态。由于它们的三维结构,它们也可能与寡糖中不相邻的糖残基相互作用,这可能通过排除水导致有序结构。另一方面,β连接键(连接到3-和4-位)保持强氢键,参与水桥的能力有限,并且主要与直接连接的糖相互作用。因此,α连接的糖序列形成具有构象灵活性的紧凑、分支结构,而β连接键形成适合于结构分子以及蛋白质结合寡糖末端的延伸、相对刚性的结构。这些结果进一步提供了化学结构、水相互作用以及寡糖中特定糖和连接键的新兴形式和功能之间的初步联系。