Suppr超能文献

固相糖脂结合分析测定抗-αGal 试剂的抗原结合特异性。α1,3GalT-KO 猪小肠中完全缺乏 αGal 糖脂反应性。

Antigen-binding specificity of anti-αGal reagents determined by solid-phase glycolipid-binding assays. A complete lack of αGal glycolipid reactivity in α1,3GalT-KO pig small intestine.

机构信息

Department of Surgery, Sahlgrenska Academy at Gothenburg University, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Xenotransplantation. 2011 Jan-Feb;18(1):28-39. doi: 10.1111/j.1399-3089.2011.00623.x.

Abstract

BACKGROUND

αGal-specific lectins, monoclonal and polyclonal antibodies (Abs) are widely used in xenotransplantation research. Immunological assays such as immunohistochemistry, flow cytometry, Western blot and thin layer chromatography are often the only applicable characterization procedures when limited amount of tissue is available and biochemical characterization is impossible. Hence, detailed knowledge of the Ab/lectin carbohydrate-binding specificity is essential.

METHODS

The binding specificity of human blood group AB serum, three different affinity-purified human polyclonal anti-Gal Ab batches, and two anti-Gal mAb clones (TH5 and 15.101) as well as Griffonia simplicifolia isolectin B4 and Marasmius oreades agglutinin were examined for reactivity with glycolipid fractions isolated from human and pig (wild-type and α1,3GalT-KO) tissues using thin layer chromatogram and microtiter well binding assays.

RESULTS

All anti-Gal-specific reagents reacted with the pentaglycosylceramide Galα1,3nLc4, and several 6-12 sugar compounds in wild-type pig kidneys. However, their staining intensity with different αGal antigens varied considerably. Some, but not all, anti-Gal reagents cross-reacted with a pure iGb3 glycolipid reference compound. No reactivity with glycolipids isolated from α1,3GalT-KO pig small intestine or human tissues was found, confirming the specificity of the anti-Gal reagents in those tissues for α1,3Gal-epitopes produced by the α1,3GalT (GGTA1).

CONCLUSIONS

Different anti-Gal reagents vary in their carbohydrate epitope specificity. Mono-/polyclonal Abs and lectins have different carbohydrate epitope fine specificity toward pig glycolipids as well as purified Galα1,3nLc4, and iGb3. Despite the difference in αGal specificity, all reagents were completely non-reactive with glycolipids isolated from α1,3GalT-KO pig small intestine.

摘要

背景

αGal 特异性凝集素、单克隆和多克隆抗体(Abs)广泛应用于异种移植研究。当组织量有限且无法进行生化特性分析时,免疫组织化学、流式细胞术、Western blot 和薄层色谱等免疫测定方法通常是唯一适用的鉴定程序。因此,详细了解 Ab/凝集素的碳水化合物结合特异性至关重要。

方法

使用薄层色谱和微量滴定孔结合测定法,检测人 AB 型血清、三种不同亲和纯化的人多克隆抗 Gal Ab 批次以及两种抗 Gal mAb 克隆(TH5 和 15.101)以及 Griffonia simplicifolia isolectin B4 和 Marasmius oreades 凝集素与人和猪(野生型和 α1,3GalT-KO)组织中分离的糖脂级分的反应性。

结果

所有抗 Gal 特异性试剂均与五糖神经酰胺 Galα1,3nLc4 以及野生型猪肾脏中的几种 6-12 糖化合物发生反应。然而,它们与不同的αGal 抗原的染色强度差异很大。一些但不是所有的抗 Gal 试剂与纯 iGb3 糖脂参考化合物发生交叉反应。从 α1,3GalT-KO 猪小肠或人组织中分离的糖脂未发现任何反应性,证实了这些组织中抗 Gal 试剂对由 α1,3GalT(GGTA1)产生的α1,3Gal 表位的特异性。

结论

不同的抗 Gal 试剂在其碳水化合物表位特异性上存在差异。单克隆/多克隆 Abs 和凝集素对猪糖脂以及纯化的 Galα1,3nLc4 和 iGb3 的碳水化合物表位具有不同的精细特异性。尽管 αGal 特异性存在差异,但所有试剂与从 α1,3GalT-KO 猪小肠中分离的糖脂完全没有反应性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验