Kabir S
Department of Immunology, Karolinska Institute, Stockholm, Sweden.
Comp Immunol Microbiol Infect Dis. 1993 Apr;16(2):153-61. doi: 10.1016/0147-9571(93)90008-s.
Immunoglobulins of IgA and IgG isotypes are formed in host intestines after enteric infections with bacteria such as Vibrio cholerae. A method has been developed for the separation of intestinal immunoglobulins from rabbits immunized intraduodenally with live V. cholerae cells by sequential affinity chromatography on immobilized jacalin and immobilized protein A. The jacalin-Sepharose 4B bound IgA was desorbed with 0.5 M galactose. The protein A-Sepharose 4B bound IgG was desorbed with 0.1 M citrate buffer. The quality of the isolated IgA and IgG was checked by immunodiffusion in agarose gels, enzyme-linked immunosorbent assay and sodium dodecyl sulphate-polyacrylamide gel electrophoresis. The procedure described here is rapid and convenient. It can be used to isolate intestinal IgA and IgG in pure form.
在肠道受到霍乱弧菌等细菌感染后,宿主肠道中会形成IgA和IgG亚型的免疫球蛋白。已开发出一种方法,通过在固定化红豆凝集素和固定化蛋白A上进行连续亲和层析,从经十二指肠接种活霍乱弧菌细胞免疫的兔子中分离肠道免疫球蛋白。用0.5M半乳糖使结合在红豆凝集素-琼脂糖4B上的IgA解吸。用0.1M柠檬酸盐缓冲液使结合在蛋白A-琼脂糖4B上的IgG解吸。通过琼脂糖凝胶免疫扩散、酶联免疫吸附测定和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳检查分离出的IgA和IgG的质量。这里描述的方法快速且方便。它可用于以纯形式分离肠道IgA和IgG。