Xu Q, Mohan S, Bush C A
Department of Chemistry and Biochemistry, University of Maryland, Baltimore 21228, USA.
Biopolymers. 1996 Mar;38(3):339-53. doi: 10.1002/(SICI)1097-0282(199603)38:3%3C339::AID-BIP7%3E3.0.CO;2-V.
We report on the conformation of a tetrasaccharide fragment in the repeating subunit of the cell wall polysaccharide of Streptococcus mitis J22, a receptor for the lectin of Actinomyces viscosus T14V in a bacterial coaggregation that is important in the ecological interactions of oral bacteria. Although there is considerable overlap of the 1H-nmr signals, some cross peaks can be extracted from conventional two-dimensional nuclear Overhauser effect spectroscopy (NOESY) data on the polysaccharide. These data cannot be fit to a single conformation of the tetrasaccharide fragment. Therefore we have prepared a polysaccharide sample fully enriched in 13C from which we have determined accurate NOESY cross-peak volumes in a three-dimensional heteronuclear-resolved spectrum that allows accurate determination of many more NOESY cross peaks than does conventional two-dimensional spectroscopy. We have also used the 13C enriched polysaccharide to measure accurate values of long-range 13C-1H coupling constants that can be correlated with glycosidic dihedral angles. Molecular modeling calculations on the polysaccharide fragment, including molecular dynamics simulations, identify multiple low-energy conformations. This result is to be contrasted with previous calculations on blood group oligosaccharides in our laboratory using similar methods that showed relatively rigid conformations with little flexibility of the glycosidic linkages. The present NOESY and 3JCH data can be reconciled with a model for the antigenic tetrasaccharide in which three distinct conformations are in fast exchange. We propose that some carbohydrate epitopes such as those of the blood group oligosaccharides are relatively rigid while others such as the tetrasaccharide fragment in these studies exhibit much greater flexibility.
我们报道了缓症链球菌J22细胞壁多糖重复亚基中四糖片段的构象,该多糖是粘性放线菌T14V凝集素在细菌共聚作用中的受体,而这种共聚作用在口腔细菌的生态相互作用中很重要。尽管1H-nmr信号有相当大的重叠,但仍可从多糖的传统二维核Overhauser效应光谱(NOESY)数据中提取一些交叉峰。这些数据无法拟合到四糖片段的单一构象。因此,我们制备了完全富含13C的多糖样品,从中我们在三维异核分辨光谱中确定了准确的NOESY交叉峰体积,与传统二维光谱相比,该光谱能准确测定更多的NOESY交叉峰。我们还使用富含13C的多糖来测量可与糖苷二面角相关的远程13C-1H耦合常数的准确值。对多糖片段进行的分子建模计算,包括分子动力学模拟,确定了多个低能量构象。这一结果与我们实验室之前使用类似方法对血型寡糖进行的计算形成对比,之前的计算显示其构象相对刚性,糖苷键的灵活性很小。目前的NOESY和3JCH数据可以与抗原四糖的模型相吻合,在该模型中三种不同的构象处于快速交换状态。我们提出,一些碳水化合物表位,如血型寡糖的表位,相对刚性,而其他一些表位,如本研究中的四糖片段,则表现出更大的灵活性。