Okuda Tetsuya, Fukui Asami
Bio-Design Research Group, Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan; Molecular and Biological Technology Research Group, Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Sapporo, Japan.
Molecular and Biological Technology Research Group, Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Sapporo, Japan.
Biochem Biophys Res Commun. 2018 Mar 18;497(4):983-989. doi: 10.1016/j.bbrc.2018.02.113. Epub 2018 Feb 16.
Here we report a new method for the efficient generation of antibodies that recognize the fine structures of oligosaccharides on glycoproteins. We found a newly designed artificial glycosphingolipid carrying a very long chain fatty acid to be a strong immunogen in mice, with the serum of immunized mice containing antibodies recognizing the oligosaccharide structure of the immunogen. First, we found that conjugation of a simple ceramide analogue to target oligosaccharides could enhance the immunogenicity of these oligosaccharides in these immunized mice. This effect was confirmed in mice immunized with the artificial glycosphingolipids carrying 6'-Sialyl-LacNAc, 3'-Sialyl-LacNAc and LacNAc. Next, we tried to improve the immunogenic enhancing effect of the ceramide analogue. In a model experiment using 6'-Sialyl-LacNAc oligosaccharide, we manipulated the alkyl chains to several lengths, and found that a longer alkyl chain length of the fatty acid correlated with high immunogenicity. Among these we examined, artificial glycosphingolipids conjugated with a ceramide analogue carrying a very long chain fatty acid (lignoceric acid) showed the strongest immunogenicity. By using the artificial glycosphingolipid containing 6'-Sialy-LacNAc and lignoceric acid, we succeeded in the generation of a new anti-6'-Sialyl-LacNAc antibody that recognizes 6'-Sialyl-LacNAc carrying glycoproteins but does not bind to 6'-Sialyllactose, asialo-glycoporoteins and glycoproteins carrying 3'-Sialyl-LacNAc. These results indicate that the established technology is valuable for the targeted generation of monoclonal antibodies against glycoproteins containing specific oligosaccharide structures.
在此,我们报告一种高效生成识别糖蛋白上寡糖精细结构抗体的新方法。我们发现一种新设计的携带超长链脂肪酸的人工糖鞘脂在小鼠中是一种强免疫原,免疫小鼠的血清中含有识别该免疫原寡糖结构的抗体。首先,我们发现将一种简单的神经酰胺类似物与目标寡糖偶联可增强这些寡糖在这些免疫小鼠中的免疫原性。在用携带6'-唾液酸乳糖胺、3'-唾液酸乳糖胺和乳糖胺的人工糖鞘脂免疫的小鼠中证实了这种效果。接下来,我们试图提高神经酰胺类似物的免疫增强效果。在使用6'-唾液酸乳糖胺寡糖的模型实验中,我们将烷基链调整为几种长度,发现脂肪酸的烷基链长度越长,免疫原性越高。在我们检测的这些物质中,与携带超长链脂肪酸(木蜡酸)的神经酰胺类似物偶联的人工糖鞘脂显示出最强的免疫原性。通过使用含有6'-唾液酸乳糖胺和木蜡酸的人工糖鞘脂,我们成功生成了一种新的抗6'-唾液酸乳糖胺抗体,该抗体识别携带6'-唾液酸乳糖胺的糖蛋白,但不与6'-唾液酸乳糖、去唾液酸糖蛋白和携带3'-唾液酸乳糖胺的糖蛋白结合。这些结果表明,所建立的技术对于靶向生成针对含有特定寡糖结构的糖蛋白的单克隆抗体具有重要价值。