Apold J, Florvaag E, Elsayed S
Int Arch Allergy Appl Immunol. 1981;64(4):439-47.
A major allergen from birch pollen (Betula verrucosa) was isolated by a combination of gel permeation chromatography and preparative isoelectric focusing, and was found adequate for further immunological and chemical characterization. The crude aqueous pollen extract was eluted in 6 UV-absorbance peaks from an Ultrogel AcA-54 column. The main allergenic components were detected in two peaks of molecular weights 29,000 (BV4) and 40,000 daltons, respectively. BV4 contained one quantitatively dominating antigen as assessed by crossed immunoelectrophoresis, and was selected for further purification by isoelectric focusing. Column isoelectric focusing of BV4 gave four protein fractions with pI values corresponding to 5.18, 5.42, 5.76, and 5.94. The pI 5.18 protein was quantitatively dominating. This protein inhibited the radio-allergosorbent test in 8 out of 10 sera from birch pollen-sensitive individuals. Using a serum pool, the inhibition curve of BV4 pI 5.18 was parallel to that of the crude extract and gave a similar maximum inhibition. This allergen was shown to be homogeneous as judged by a single, symmetrical precipitate in crossed immunoelectrophoresis, one band in high-volt electrophoresis and a sharp strip in thin-layer analytical electrofocusing. Amino acid analysis showed a high content of serine. The N-terminal analysis as well as the carbohydrate concentration were preliminarily reported and will be confirmed in future studies.
通过凝胶渗透色谱法和制备性等电聚焦相结合的方法,从桦树花粉(疣枝桦)中分离出一种主要过敏原,并发现其足以进行进一步的免疫学和化学特性分析。粗制的水性花粉提取物从Ultrogel AcA - 54柱上以6个紫外吸收峰洗脱。主要过敏原成分分别在分子量为29,000(BV4)和40,000道尔顿的两个峰中检测到。通过交叉免疫电泳评估,BV4含有一种在数量上占主导的抗原,并被选择通过等电聚焦进行进一步纯化。BV4的柱等电聚焦得到四个蛋白质组分,其pI值分别对应于5.18、5.42、5.76和5.94。pI为5.18的蛋白质在数量上占主导。这种蛋白质在10份来自桦树花粉敏感个体的血清中有8份抑制了放射变应原吸附试验。使用混合血清,BV4 pI 5.18的抑制曲线与粗提取物的抑制曲线平行,并给出了相似的最大抑制率。通过交叉免疫电泳中的单一对称沉淀、高压电泳中的一条带以及薄层分析电聚焦中的一条清晰条带判断,该过敏原显示为均一的。氨基酸分析表明丝氨酸含量很高。初步报道了N端分析以及碳水化合物浓度,未来研究将予以证实。