Victoria E J, Branks M J, Masouredis S P
Transfusion. 1987 Jan-Feb;27(1):32-5. doi: 10.1046/j.1537-2995.1987.27187121469.x.
Skeleton-free microvesicles derived from D-positive red cells immunospecifically bind anti-D. Anti-D saturation binding yielded an equilibrium constant value (K = 1-2 X 10(8) I mole-1) similar to intact red cells. The vesicles contained band 3, the major sialoglycoproteins and, at high protein loads, low-molecular-weight polypeptides. Anti-D binding was referenced to total protein, phospholipid, and band 3 content to determine whether there was nonrandom segregation of the D antigen into vesicles. Selective segregation of the D antigen into vesicles could not be demonstrated unequivocally based on the methods and the assumptions of this study. The results, however, indicate that D reactivity does not require a membrane skeletal association.
来源于D阳性红细胞的无骨架微泡能免疫特异性结合抗-D。抗-D饱和结合产生的平衡常数(K = 1 - 2×10⁸ I mol⁻¹)与完整红细胞相似。这些微泡含有带3蛋白、主要的唾液糖蛋白,在高蛋白负载时还含有低分子量多肽。抗-D结合以总蛋白、磷脂和带3蛋白含量为参照,以确定D抗原是否非随机地分离到微泡中。基于本研究的方法和假设,无法明确证明D抗原选择性地分离到微泡中。然而,结果表明D反应性并不需要与膜骨架相关联。