Department of Molecular Physiology, Niigata University School of Medicine, Niigata, Japan.
Department of Otorhinolaryngology-Head and Neck Surgery, Niigata University School of Medicine, Niigata, Japan.
Sci Rep. 2019 Feb 7;9(1):1551. doi: 10.1038/s41598-018-38079-0.
Membrane proteins (such as ion channels, transporters, and receptors) and secreted proteins are essential for cellular activities. N-linked glycosylation is involved in stability and function of these proteins and occurs at Asn residues. In several organs, profiles of N-glycans have been determined by comprehensive analyses. Nevertheless, the cochlea of the mammalian inner ear, a tiny organ mediating hearing, has yet to be examined. Here, we focused on the stria vascularis, an epithelial-like tissue in the cochlea, and characterised N-glycans by liquid chromatography with mass spectrometry. This hypervascular tissue not only expresses several ion transporters and channels to control the electrochemical balance in the cochlea but also harbours different transporters and receptors that maintain structure and activity of the organ. Seventy-nine N-linked glycans were identified in the rat stria vascularis. Among these, in 55 glycans, the complete structures were determined; in the other 24 species, partial glycosidic linkage patterns and full profiles of the monosaccharide composition were identified. In the process of characterisation, several sialylated glycans were subjected sequentially to two different alkylamidation reactions; this derivatisation helped to distinguish α2,3-linkage and α2,6-linkage sialyl isomers with mass spectrometry. These data should accelerate elucidation of the molecular architecture of the cochlea.
膜蛋白(如离子通道、转运蛋白和受体)和分泌蛋白是细胞活动所必需的。N-连接糖基化参与这些蛋白质的稳定性和功能,并发生在 Asn 残基上。在几个器官中,通过综合分析已经确定了 N-聚糖的图谱。然而,哺乳动物内耳的耳蜗——一个介导听力的微小器官——尚未被检测到。在这里,我们专注于血管纹,耳蜗中的一种上皮样组织,并通过液相色谱-质谱法对 N-聚糖进行了表征。这个高度血管化的组织不仅表达了几种离子转运体和通道来控制耳蜗中的电化学平衡,还拥有不同的转运体和受体,维持着器官的结构和功能。在大鼠血管纹中鉴定出了 79 种 N-连接聚糖。在这些糖中,有 55 种糖的完整结构被确定;在其他 24 种糖中,鉴定出了部分糖苷键模式和单糖组成的完整图谱。在表征过程中,几种唾液酸化聚糖依次进行了两种不同的烷基酰胺化反应;这种衍生化有助于通过质谱法区分α2,3-连接和α2,6-连接唾液酸异构体。这些数据应该会加速耳蜗的分子结构的阐明。