Schenkel-Brunner H
Wien Klin Wochenschr. 1980 Nov 7;92(21):749-51.
Human O and A2 erythrocytes were incubated with the alpha-N-acetyl-galactosaminyltransferases isolated from the plasma of A1 and A2 individuals in the presence of labelled UDP-N-acetylgalactosamine. It could be shown that both O and A2 cells could be agglutinated by anti-A1 reagent when treated with the A2 transferase. Furthermore, the incorporated radioactivity was about equal for both cell types, corresponding to about 600.000 A sites newly formed; this number, however, is considerably higher than that found in native A2 cells (i.e. about 260.000). The results presented thus provide good evidence that the development of the subgroups A1 and A2 is based mainly on differences in enzyme kinetics of the A1 and A2 gene-dependent N-acetylgalactosaminyltransferases, rather than on variations in their substrate specificities.
将人O型和A2型红细胞与从A1型和A2型个体血浆中分离出的α-N-乙酰半乳糖胺基转移酶一起,在标记的UDP-N-乙酰半乳糖胺存在的情况下进行孵育。结果表明,当用A2转移酶处理时,O型和A2型细胞都能被抗A1试剂凝集。此外,两种细胞类型掺入的放射性大致相等,对应于新形成的约600,000个A位点;然而,这个数字远高于天然A2细胞中的数量(即约260,000个)。因此,所呈现的结果充分证明,A1和A2亚组的形成主要基于A1和A2基因依赖性N-乙酰半乳糖胺基转移酶的酶动力学差异,而非其底物特异性的变化。