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首页> 外文期刊>Journal of Virology >Monosaccharide Sequence of Protein-Bound Glycans of Uukuniemi Virus
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Monosaccharide Sequence of Protein-Bound Glycans of Uukuniemi Virus

机译:uukuniemi病毒的蛋白质结合聚糖的单糖序列

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Uukuniemi virus, a member of the Bunyaviridae family, was grown in BHK-21 cells in the presence of [3H]mannose. The purified virions were disrupted with sodium dodecyl sulfate and digested with pronase. The [3H]mannose-labeled glycopeptides of the mixture of the two envelope glycoproteins G1 and G2 were characterized by degrading the glycans with specific exo-and endoglycosidases, by chemical methods, and by analyzing the products with lectin affinity and gel chromatography. The glycopeptides of Uukuniemi virus fell into three categories: complex, high-mannose type, and intermediate. The complex glycopeptides probably contained mainly two NeuNAc-Gal-GlcNAc branches attached to a core (Man)3(GlcNAc)2 peptide. The high-mannose-type glycans were estimated to contain at least five mannose units attached to two N-acetylglucosamine residues. Both glycan species appeared to be similar to the asparagine-linked oligosaccharides found in many soluble and membrane glycoproteins. The results suggested that the intermediate glycopeptides contained a mannosyl core. In about half of the molecules, one branch appeared to be terminated in mannose, and one appeared to be terminated in N-acetylglucosamine. Such glycans are a novel finding in viral membrane proteins. They may represent intermediate species in the biosynthetic pathway from high-mannose-type to complex glycans. Their accumulation could be connected with the site of maturation of the members of the Bunyaviridae family. Electron microscopic data suggest that the virions bud into smooth-surfaced cisternae in the Golgi region. The relative amounts of [3H]mannose in the complex, high-mannose-type, and intermediate glycans were 25, 62, and 13%, respectively, which corresponded to the approximate relative number of oligosaccharide chains of 2:2.8:1, respectively, in the roughly equimolar mixture of G1 and G2. Endoglycosidase H digestion of isolated [35S]methionine-labeled G1 and G2 proteins suggested that most of the complex and intermediate chains were attached to G1 and that most of the high-mannose-type chains were attached to G2.
机译:uukuniemi病毒是Bunyaviridae家族的成员,在[ 3 h]甘露糖存在下在BHK-21细胞中生长。纯化的病毒粒子用十二烷基硫酸钠破坏并用蛋白酶消化。通过化学方法将具有特异性外糖苷和内糖苷酶的聚糖降解,并通过分析产品,通过分析产品,并通过分析产品来表征两种包膜糖蛋白G1和G2的混合物的甘露糖标记的糖肽。凝集素亲和力和凝胶色谱。 uukuniemi病毒的糖肽分为三类:复杂,高甘露糖类型和中间体。复合糖肽可能主要含有两个连接到核心(人)<亚> 3 (glcnac) 2 肽的肌瘤 - GLCNAC分支。估计高甘露糖型聚糖含有至少五个甘露糖单元,其附着在两个 N - 乙酰甘氨酸残基。糖粉种类似乎类似于许多可溶性和膜糖蛋白中发现的天冬酰胺连接的寡糖。结果表明中间糖肽含有甘露糖基核。在大约一半的分子中,一个分支似乎在甘露糖中终止,并且似乎终止于 n - 乙酰葡糖胺中。这种聚糖是病毒膜蛋白的新发现。它们可以代表生物合成途径中的中间物种从高甘露糖类型到复合聚糖。它们的积累可以与Bunyaviridae家族成员的成熟部位相关联。电子显微镜数据表明,病毒粒芽在高尔基地区的光滑表面。复合物高甘露糖型和中间聚糖中[ 3 h]甘露糖的相对量分别为25,62和13%,其对应于寡糖链的近似相对数量分别在G1和G2的大致等摩尔混合物中分别为2:2.8:1。分离的内皮糖苷酶H消化[ 35 s]甲硫氨酸标记的g1和g2蛋白表明,大多数复合链和中间链附着于g1,并且大多数高甘露糖型链附着G2。

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