[Comparative study of A, B, and H substances in stromas with and without lipid removal. Studies of the erythrocyte membrane].

A Le Bec, R Waitz
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Abstract

Human erythrocyte membranes were prepared by hypotonic hemolysis and extracted with water pH 7, EDTA and mercapto-ethanol solutions pH 8. The complex residue which contains lipids, proteins and the A, B, H antigens was dissolved in SDS and analysed by preparative acrylamide gel electrophoresis in the presence of SDS. Each fraction was assayed for A, B or H blood-group activity by hemagglutination inhibition tests. Two experiments were done for each blood-group A, B, O. One with entire ghosts, another after extraction of the ghosts residue with a mixture of chloroform-methanol. The comparison of results showed that the distribution of proteins and blood-group antigen activity among the different fractions is not modified and that, in the two experiments, the elution of H substance is delayed by comparison with elution of A and B substances. The blood-group A, B and H antigens are known to be glycosphingolipids and are not entirely eliminated by treatment of the ghosts with cloroform and methanol. It has recently been reported [7] that these antigens are complex glycosphingolipids with hydrophilic character and remain in the aqueous phase after extraction of the erythrocyte membrane with organic solvents.

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[去脂和不去脂的基质中A、B和H物质的比较研究。]红细胞膜的研究]。
采用低渗溶血法制备人红细胞膜,分别用pH为7的水、EDTA和pH为8的巯基乙醇溶液进行提取。将含有脂质、蛋白质和A、B、H抗原的复合残基溶解在SDS中,在SDS存在下用制备丙烯酰胺凝胶电泳进行分析。通过血凝抑制试验测定各组分的A、B或H血型活性。对A、B、o血型各做两次实验,一次用完整的鬼液,另一次用氯仿-甲醇混合物提取鬼液残留物。结果比较表明,蛋白质和血型抗原活性在不同组分之间的分布没有改变,并且在两个实验中,H物质的洗脱比A和B物质的洗脱延迟。已知A、B和H血型抗原是鞘糖脂,用氯仿和甲醇处理幽灵不能完全消除。最近有报道[7],这些抗原是具有亲水性的复合鞘糖脂,用有机溶剂提取红细胞膜后仍留在水相中。
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First International Workshop on Monoclonal Antibodies Against Red Blood Cell and Related Antigens. Paris, September 21-24, 1987. Vol. II: Other blood group systems. [Procurement of plasma by filtration]. First International Workshop on Monoclonal Antibodies against Human Red Blood Cells and Related Antigens. Part I: ABH and other glycoconjugates. Paris, September 21-24, 1987. [Platelet pool versus single platelet donor]. [New evaluation of 3 immunoenzyme assay kits for the detection of anti-LAV antibodies].
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