Chen K C, Kindt T J, Krause R M
J Biol Chem. 1975 May 10;250(9):3280-8.
Primary structural studies have been carried out on the light chain of a homogeneous rabbit antibody to Group C streptococcal carbohydrate. Approximately 20 g of this antibody were obtained by multiple exchange transfusions at the peak of the antibody response. The isolated antibody was homogeneous by several antigenic and chemical criteria. The light chain was isolated and modified, and then digested with alpha-chymotrypsin or thermolysin. The resulting peptides were isolated by gel filtration, paper electrophoresis, and paper chromatography. The amino acid sequences of these peptides were determined by Edman degradation plus dansylation. This supplied sufficient information to assign approximately 90 percent of the residues in the chain. The destruction of tyrosine during acid hydrolysis of peptides which had been eluted from a paper chromatogram was investigated. This destruction is due to inpurities in the paper which contaminate the peptides. Prevention of such destruction can be achieved by predevelopment of the paper with 1 N NH4OH prior to paper chromatography.
已对一种针对C组链球菌碳水化合物的同源兔抗体的轻链进行了一级结构研究。在抗体反应高峰期,通过多次换血获得了约20克这种抗体。通过多种抗原和化学标准,分离出的抗体是均一的。轻链被分离、修饰,然后用α-胰凝乳蛋白酶或嗜热菌蛋白酶消化。所得肽段通过凝胶过滤、纸电泳和纸色谱法分离。这些肽段的氨基酸序列通过埃德曼降解法加丹磺酰化法测定。这提供了足够的信息来确定轻链中约90%的残基。对从纸色谱图上洗脱下来的肽段在酸水解过程中酪氨酸的破坏情况进行了研究。这种破坏是由于纸张中的杂质污染了肽段所致。在纸色谱之前用1N氢氧化铵对纸张进行预展开可防止这种破坏。