Tsuji H, Bando N, Hiemori M, Yamanishi R, Kimoto M, Nishikawa K, Ogawa T
Department of Nutrition, School of Medicine, University of Tokushima, Japan.
Biosci Biotechnol Biochem. 1997 Jun;61(6):942-7. doi: 10.1271/bbb.61.942.
At least 15 allergenic proteins have been found in soybean using the sera of soybean-sensitive patients with atopic dermatitis [T. Ogawa et al., J. Nutr. Sci. Vitaminol., 35, 555-565 (1991)]. In the present study, a monoclonal antibody (mAb) against Gly m Bd 28K, one of the major allergens of soybean, was prepared, and Gly m Bd 28K was purified from defatted soybean flakes by five purification steps, including immunoaffinity chromatography with the mAb as a ligand. The purified allergen was found to be a glycoprotein with a molecular mass of 26 kDa. During the purification process the allergen was converted to more acidic proteins with the same molecular mass, suggesting that the allergen is unstable. The sugar composition and amino acid sequence of Gly m Bd 28K suggest that the allergen is a new glycoprotein with an Asn-linked sugar moiety. The distribution of the allergen in soybean products was examined by an immunoblotting technique with the mAb.
利用患有特应性皮炎的大豆敏感患者的血清,在大豆中已发现至少15种致敏蛋白[T. 小川等人,《营养科学与维生素学杂志》,35,555 - 565(1991)]。在本研究中,制备了一种针对大豆主要过敏原之一Gly m Bd 28K的单克隆抗体(mAb),并通过五个纯化步骤从脱脂大豆片中纯化出Gly m Bd 28K,其中包括以该mAb作为配体的免疫亲和色谱法。发现纯化后的过敏原是一种分子量为26 kDa的糖蛋白。在纯化过程中,该过敏原转化为具有相同分子量的酸性更强的蛋白质,这表明该过敏原不稳定。Gly m Bd 28K的糖组成和氨基酸序列表明,该过敏原是一种带有天冬酰胺连接糖部分的新型糖蛋白。采用mAb免疫印迹技术检测了该过敏原在大豆制品中的分布情况。