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来自猕猴(食蟹猴)腮腺唾液中的磷蛋白。富含脯氨酸的磷酸糖蛋白的分离与特性鉴定以及富含脯氨酸的磷酸肽的完整共价结构。

Phosphoproteins in the parotid saliva from the subhuman primate Macaca fascicularis. Isolation and characterization of a proline-rich phosphoglycoprotein and the complete covalent structure of a proline-rich phosphopeptide.

作者信息

Oppenheim F G, Offner G D, Troxler R F

出版信息

J Biol Chem. 1982 Aug 25;257(16):9271-82.

PMID:7107568
Abstract

Parotid saliva from the cynomolgus monkey (Macaca fascicularis) and from pooled human collections displayed the same groups of proteins when fractionated by anion exchange and gel filtration chromatography. We have isolated and characterized a proline-rich phosphoglycoprotein (MPRP) and a proline-rich phosphopeptide (M-statherin) from macaque parotid saliva. MPRP has an apparent molecular weight of 16,900 and displays an unusual chemical composition. It is enriched in proline, glycine, and acidic amino acids, but lacks cysteine, methionine, and tyrosine. MPRP contains 25% (w/w) carbohydrate with 7.0 mol of neutral hexoses, 5.3 mol of galactosamine, 5.9 mol of sialic acid, and 3 mol of phosphorus/mol of protein. M-statherin is a 42-residue phosphopeptide with a high proline, glutamic acid, and tyrosine content, but which lacks threonine, valine, cysteine, methionine, isoleucine, and histidine. The complete covalent structure of M-statherin (Mr = 5,368) is: NH2-Asp-Pse-Pse-Glu-Glu-Lys-Phe-Leu-Arg-Arg-Leu-Arg-Arg-Phe-Asp-Glu-Gly-Arg-Tyr- -Gly-Pro-Tyr-Gln-Pro-Phe-Ala-Pro-Gln-Pro-Leu-Tyr-Pro-Gln-Pro-Tyr-Gln-Pro-Tyr-Gln-Pro-Gln-Tyr-COOH This is the first complete amino acid sequence of a component in the salivary secretion of a subhuman primate. Phosphoserine occurs at residues 2 and 3. All 13 acidic and basic amino acids are located in the NH2-terminal half of the molecule. The carboxyl-terminal half of the molecule is hydrophobic where the tripeptide Tyr-Gln-Pro is repeated three times, the dipeptide Gln-Pro occurs twice, and the tripeptides Tyr-Gly-Pro, Phe-Ala-Pro, and Leu-Tyr-Pro occur once. Evaluation of secondary structure by the Chou-Fasman method predicts an alpha helix in the NH2-terminal half (residue 4-16) and a beta pleated sheet in the carboxyl-terminal half (residues 22-26; 38-42) of the molecule. Both MPRP and M-statherin inhibit spontaneous and seeded precipitation from solutions supersaturated with respect to calcium phosphate salts. This suggests that these macaque compounds may function by maintaining saliva supersaturated with respect to calcium phosphate salts, a necessary requirement for stabilization of hydroxyapatite in the surface layers of teeth.U

摘要

通过阴离子交换和凝胶过滤色谱法分级分离时,食蟹猴(猕猴)的腮腺唾液和混合的人类唾液样本显示出相同的蛋白质组。我们从猕猴腮腺唾液中分离并鉴定了一种富含脯氨酸的磷糖蛋白(MPRP)和一种富含脯氨酸的磷肽(M-牙本质磷蛋白)。MPRP的表观分子量为16,900,具有不寻常的化学组成。它富含脯氨酸、甘氨酸和酸性氨基酸,但不含半胱氨酸、甲硫氨酸和酪氨酸。MPRP含有25%(w/w)的碳水化合物,每摩尔蛋白质含有7.0摩尔中性己糖、5.3摩尔半乳糖胺、5.9摩尔唾液酸和3摩尔磷。M-牙本质磷蛋白是一种由42个残基组成的磷肽,脯氨酸、谷氨酸和酪氨酸含量高,但不含苏氨酸、缬氨酸、半胱氨酸、甲硫氨酸、异亮氨酸和组氨酸。M-牙本质磷蛋白(Mr = 5,368)的完整共价结构为:NH2-Asp-Pse-Pse-Glu-Glu-Lys-Phe-Leu-Arg-Arg-Leu-Arg-Arg-Phe-Asp-Glu-Gly-Arg-Tyr- -Gly-Pro-Tyr-Gln-Pro-Phe-Ala-Pro-Gln-Pro-Leu-Tyr-Pro-Gln-Pro-Tyr-Gln-Pro-Tyr-Gln-Pro-Gln-Tyr-COOH这是亚人类灵长类动物唾液分泌成分的首个完整氨基酸序列。磷酸丝氨酸出现在第2和第3位残基处。所有13个酸性和碱性氨基酸都位于分子的NH2末端一半。分子的羧基末端一半是疏水的,其中三肽Tyr-Gln-Pro重复三次,二肽Gln-Pro出现两次,三肽Tyr-Gly-Pro、Phe-Ala-Pro和Leu-Tyr-Pro各出现一次。用Chou-Fasman方法评估二级结构预测,分子的NH2末端一半(第4-16位残基)有一个α螺旋,羧基末端一半(第22-26位残基;38-42位残基)有一个β折叠片。MPRP和M-牙本质磷蛋白都能抑制相对于磷酸钙盐过饱和溶液的自发沉淀和晶种沉淀。这表明这些猕猴化合物可能通过使唾液相对于磷酸钙盐保持过饱和来发挥作用,这是牙齿表面层中羟基磷灰石稳定的必要条件。

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