Webster D M, Fisher W K, Koureas D D, Thompson E O
Aust J Biol Sci. 1981;34(5-6):505-14. doi: 10.1071/bi9810505.
Ovalbumin isolated from eggs of the Japanese quail, C. c. japonica, was subjected to limited proteolysis by subtilisin to give plakalbumin and then fractionated on Sephadex G75 in acid-urea to give plakalbumin S-protein and S-peptide. The plakalbumin peptide was recovered, oxidized with performic acid, and the sequence of amino acids determined from the peptides formed by enzyme digestion. There were two cysteine residues in the 33-residue sequence. The ovalbumin was also oxidized with performic acid and digested with thermolysin and pepsin before isolating, from a sulfonated polystyrene column, the acidic cysteic acid peptides, as well as acetylated N-terminal peptides and phosphorylated peptides, and determining their amino acid sequence. Additional peptide sequences containing cysteine or half-cystine were characterized. Quail ovalbumin was reduced and carboxymethylated with [2-14C]iodoacetic acid. Peptides containing labelled S-carboxymethylcysteine residues were isolated from thermolytic digests of the carboxymethylated ovalbumin by paper ionophoresis and chromatography. Their amino acid sequence was determined and five different sequences involving labelled S-carboxymethylcysteine residues were established. The presence of two half-cystine residues and the location of the disulfide bond were shown by blocking the cysteine residues with non-radioactive iodoacetic acid, reducing the disulfide bond and labelling the half-cystine residues with [2-14C]iodoacetic acid. After thermolytic digestion of the protein, radioactive peptides were isolated by paper ionophoresis and chromatography. These studies have thus shown that quail ovalbumin contains one cystine residue and three cysteine residues, which is one residue of cysteine less than in ovalbumin from the hen (Gallus gallus domesticus). There is strong homology in the amino acid sequences of hen ovalbumin and quail ovalbumin determined in these investigations.
从日本鹌鹑(C. c. japonica)的卵中分离出的卵清蛋白,用枯草杆菌蛋白酶进行有限度的蛋白水解得到 plakalbumin,然后在酸性尿素条件下于 Sephadex G75 上进行分级分离,得到 plakalbumin S-蛋白和 S-肽。回收 plakalbumin 肽,用过甲酸氧化,通过酶消化形成的肽来确定氨基酸序列。在 33 个残基的序列中有两个半胱氨酸残基。卵清蛋白也用过甲酸氧化,并用嗜热菌蛋白酶和胃蛋白酶消化,然后从磺化聚苯乙烯柱上分离出酸性半胱氨酸肽、乙酰化 N 端肽和磷酸化肽,并确定它们的氨基酸序列。鉴定了其他含有半胱氨酸或半胱氨酸残基的肽序列。鹌鹑卵清蛋白用[2-14C]碘乙酸进行还原和羧甲基化。通过纸电泳和色谱法从羧甲基化卵清蛋白的嗜热菌蛋白酶消化物中分离出含有标记的 S-羧甲基半胱氨酸残基的肽。确定了它们的氨基酸序列,并建立了涉及标记的 S-羧甲基半胱氨酸残基的五种不同序列。通过用非放射性碘乙酸封闭半胱氨酸残基、还原二硫键并用[2-14C]碘乙酸标记半胱氨酸残基,显示了两个半胱氨酸残基的存在和二硫键的位置。蛋白质经嗜热菌蛋白酶消化后,通过纸电泳和色谱法分离出放射性肽。这些研究表明,鹌鹑卵清蛋白含有一个胱氨酸残基和三个半胱氨酸残基,比家鸡(Gallus gallus domesticus)的卵清蛋白少一个半胱氨酸残基。在这些研究中确定的家鸡卵清蛋白和鹌鹑卵清蛋白的氨基酸序列有很强的同源性。