Carlstedt I, Herrmann A, Karlsson H, Sheehan J, Fransson L A, Hansson G C
Department of Physiological Chemistry 2, University of Lund, Sweden.
J Biol Chem. 1993 Sep 5;268(25):18771-81.
The highly glycosylated domains of rat small intestinal mucins were isolated after reduction and trypsin digestion and separated into two populations (A and B) by gel chromatography. The molecular mass values were 650 and 335 kDa, respectively, and the relative yields suggest that the two glycopeptides occur in equimolar proportions. Electron microscopy revealed linear structures with weight average lengths of 230 nm (A) and 110 nm (B) corresponding to a mass/unit length of about 3 kDa/nm. The protein cores (17-19%) contain large amounts of threonine (over 40%), serine (17-24%), and proline (18-19%). Carbohydrate and sulfate account for approximately 80 and 0.5%, respectively, and gas chromatography-mass spectrometry showed that the patterns of neutral and sialic acid-containing glycans are very similar in the two glycopeptides. Both contain a significant amount (7-10 mol %) of single GalNAc residues, the average oligosaccharide is about 4 sugar residues long, and the largest species observed are heptasaccharides. The major neutral and sialic acid-containing oligosaccharides are Fuc1-2Gal1-3GalNAcol and GlcNAc1-6(NeuGc2-Gal1-3)GalNAcol, respectively. Sialic acid is present as both N-acetyl- and N-glycoloyl-neuraminic acid. Repeated extractions of the tissue with guanidinium chloride left approximately 80% of the mucus glycoproteins as an insoluble glycoprotein complex whereas exposure to dithiothreitol or high speed homogenization accomplished complete solubilization. The "subunits" obtained after reduction with dithiothreitol are larger than glycopeptides A and B, and fragments corresponding in size to the latter are obtained after cleavage with trypsin. Most of the mucins from rat small intestine thus occurs as an insoluble glycoprotein complex composed of subunits joined with disulfide bonds. The subunits contain two highly glycosylated regions with different lengths substituted with very similar oligosaccharides.
大鼠小肠黏蛋白的高糖基化结构域在还原和胰蛋白酶消化后被分离出来,并通过凝胶色谱法分为两个群体(A和B)。分子量值分别为650和335 kDa,相对产量表明这两种糖肽以等摩尔比例存在。电子显微镜显示线性结构,重均长度分别为230 nm(A)和110 nm(B),对应于约3 kDa/nm的质量/单位长度。蛋白质核心(17 - 19%)含有大量的苏氨酸(超过40%)、丝氨酸(17 - 24%)和脯氨酸(18 - 19%)。碳水化合物和硫酸盐分别约占80%和0.5%,气相色谱 - 质谱分析表明,两种糖肽中中性和含唾液酸聚糖的模式非常相似。两者都含有大量(7 - 10摩尔%)的单个GalNAc残基,平均寡糖约为4个糖残基长,观察到的最大种类是七糖。主要的中性和含唾液酸寡糖分别是Fuc1 - 2Gal1 - 3GalNAcol和GlcNAc1 - 6(NeuGc2 - Gal1 - 3)GalNAcol。唾液酸以N - 乙酰 - 和N - 糖基 - 神经氨酸的形式存在。用氯化胍反复提取组织后,约80%的黏液糖蛋白作为不溶性糖蛋白复合物残留,而暴露于二硫苏糖醇或高速匀浆可实现完全溶解。用二硫苏糖醇还原后得到的“亚基”比糖肽A和B大,用胰蛋白酶切割后得到与后者大小相当的片段。因此,大鼠小肠中的大多数黏蛋白以由通过二硫键连接的亚基组成的不溶性糖蛋白复合物的形式存在。这些亚基包含两个高度糖基化的区域,长度不同,但被非常相似的寡糖取代。