Beeley J G
Biochem J. 1976 Nov;159(2):335-45. doi: 10.1042/bj1590335.
Tryptic glycopeptides were purified from the sialic acid-free variant of ovomucoid, O1, and its CNBr fragments. The amino acid sequences adjacent to the four major sites of carbohydrate (Carb.) attachment were: (1), Phe-Pro-Asn(Carb.)-Ala-Thr-Asp-Lys-Glu-Gly-Lys; (2), Ala-Try-Ser-Ile-Glu-Phe-Gly-Thr-Asn (Carb.)-Ile-Ser-Lys; (3), Glu, Thr-Val-Pro-Met-Asn(Carb.)-cys-Ser; (4), Ser-Ser-Tyr-Ala-Asn (Carb.)-Thr-Thr-Ser-Glu-Asp-Gly-Lys, Glycosylated Asn residues were located at position 10, between residues 49 and 60, and at positions 69 and 75, in the primary sequence. All of these carbohydrate groups contained GlcNAc, Man and Gal in the approximate molar proprotions 5:3:0.5. A further glycopeptide containing His was isolated in low yield, suggesting that some carbohydrate is attached at a fifth site. Two of the carbohydrate-attachment sites (Asn-10 and Asn-75) occur in sequences that show internal homologies. These are presumed to have evolved as a consequence of partial gene duplication. Three of the carbohydrate-attachment sites occur in similar positions to the carbohydrate groups in quail ovomucoid [Laskowski (1976) Protides Biol. Fluids Proc. Colloq. 23, in the press]. Prediction of peptide conformation from the sequence data by the method of Chou & Fasman [(1974) Biochemistry 13, 222-225] indicated that four glycosylated Asn residues in hen ovomucoid are very close to groups of amino acids that occur with high frequency in beta-turns. The possible significance of peptide-chain conformation in the attachment of carbohydrate to glycoproteins is briefly discussed.
从无唾液酸的类卵黏蛋白变体O1及其溴化氰片段中纯化出胰蛋白酶消化的糖肽。与四个主要碳水化合物(Carb.)连接位点相邻的氨基酸序列为:(1)苯丙氨酸-脯氨酸-天冬酰胺(Carb.)-丙氨酸-苏氨酸-天冬氨酸-赖氨酸-谷氨酸-甘氨酸-赖氨酸;(2)丙氨酸-色氨酸-丝氨酸-异亮氨酸-谷氨酸-苯丙氨酸-甘氨酸-苏氨酸-天冬酰胺(Carb.)-异亮氨酸-丝氨酸-赖氨酸;(3)谷氨酸、苏氨酸-缬氨酸-脯氨酸-甲硫氨酸-天冬酰胺(Carb.)-半胱氨酸-丝氨酸;(4)丝氨酸-丝氨酸-酪氨酸-丙氨酸-天冬酰胺(Carb.)-苏氨酸-苏氨酸-丝氨酸-谷氨酸-天冬氨酸-甘氨酸-赖氨酸。糖基化的天冬酰胺残基在一级序列中的位置为第10位、第49和60位之间以及第69和75位。所有这些碳水化合物基团中GlcNAc、甘露糖和半乳糖的摩尔比例约为5:3:0.5。还以低产率分离出一种含组氨酸的糖肽,这表明在第五个位点上有一些碳水化合物连接。其中两个碳水化合物连接位点(天冬酰胺-10和天冬酰胺-75)所在的序列显示出内部同源性。推测这是部分基因重复的结果。其中三个碳水化合物连接位点与鹌鹑类卵黏蛋白中的碳水化合物基团位置相似[拉斯科夫斯基(1976年)《生物流体中的蛋白质,会议论文集》第23卷,即将出版]。用周和法斯曼[(1974年)《生物化学》第13卷,222 - 225页]的方法根据序列数据预测肽构象表明,母鸡类卵黏蛋白中的四个糖基化天冬酰胺残基非常靠近β-转角中高频出现的氨基酸基团。简要讨论了肽链构象在碳水化合物与糖蛋白连接中的可能意义。