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小鼠乳汁中分泌型IgA的纯化与测定

Purification and measurement of secretory IgA in mouse milk.

作者信息

Parr E L, Bozzola J J, Parr M B

机构信息

Department of Anatomy, Southern Illinois University, Carbondale 62901, USA.

出版信息

J Immunol Methods. 1995 Mar 27;180(2):147-57. doi: 10.1016/0022-1759(94)00310-s.

Abstract

An important factor limiting better understanding of the protective role of sIgA at mucosal surfaces is the limited availability of the purified immunoglobulin. Among other things, purified sIgA is needed for use as a standard in measurements of the concentration of this immunoglobulin in mucosal secretions, particularly in mice, where several models of mucosal infections are available. We describe here a simple method by which one can obtain a mean of 3.5 ml of milk per mouse without a breast pump. Immunoblotting studies after native PAGE demonstrated that the milk contained mainly 420 kDa dimeric sIgA and higher polymeric forms of sIgA; only a trace of monomeric IgA was present. Similar immunoblotting studies after SDS-PAGE revealed that a portion of the sIgA was dissociated by this treatment. The 420 kDa sIgA was purified by salt fractionation, gel filtration, and affinity chromatography, and the purity of the final product was demonstrated by immunoblot analysis of biotinylated polypeptides after reduction of biotinylated protein. The concentration of 420 kDa sIgA in whey was measured by densitometry of immunoblot bands, using the purified 420 kDa sIgA as a standard, and found to be 1.0 +/- 0.3 mg/ml.

摘要

限制人们更好地理解分泌型免疫球蛋白A(sIgA)在黏膜表面保护作用的一个重要因素是纯化免疫球蛋白的可得性有限。其中,纯化的sIgA需要用作测量黏膜分泌物中这种免疫球蛋白浓度的标准,特别是在小鼠中,因为有多种黏膜感染模型。我们在此描述一种简单方法,无需使用吸奶器,每只小鼠平均可获得3.5毫升乳汁。天然聚丙烯酰胺凝胶电泳(PAGE)后的免疫印迹研究表明,乳汁中主要含有420 kDa的二聚体sIgA和更高聚合形式的sIgA;仅存在微量的单体IgA。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)后的类似免疫印迹研究显示,部分sIgA经此处理后发生解离。通过盐分级分离、凝胶过滤和亲和层析纯化420 kDa的sIgA,并通过对生物素化蛋白还原后的生物素化多肽进行免疫印迹分析来证明最终产物的纯度。以纯化的420 kDa sIgA为标准,通过免疫印迹条带的光密度测定法测量乳清中420 kDa sIgA的浓度,结果发现为1.0 +/- 0.3毫克/毫升。

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