Moriyasu M, Ito A
Cell Struct Funct. 1986 Dec;11(4):351-8. doi: 10.1247/csf.11.351.
The procedure for immunochemical adsorption of vesicles with specific antigen on their outer surfaces was improved. When microsomal vesicles were mixed with Staphylococcus aureus cells coated with the antibody against NADPH-cytochrome c reductase, more than 90% of the enzyme activity was adsorbed on the cell, whereas, only about 10% of the activity was adsorbed on cells coated with the same amount of anti-ovalbumin antibody. NADH-cytochrome c reductase and aldehyde dehydrogenase activities were adsorbed on the cell to the same extent as was NADPH-cytochrome c reductase activity. Under this condition, there was no adsorption of the activities of the marker enzymes of lysosomes and Golgi apparatus, whereas large amounts of the activities of the plasma membrane enzymes were adsorbed. The specific activity of NADPH-cytochrome c reductase in the adsorbed vesicles from the microsomal fractions increased considerably. In contrast, marker enzymes of the Golgi or of the plasma membranes could be enriched in unadsorbed vesicles from the Golgi fractions.
改进了用外表面带有特异性抗原的囊泡进行免疫化学吸附的方法。当微粒体囊泡与包被有抗NADPH - 细胞色素c还原酶抗体的金黄色葡萄球菌细胞混合时,超过90%的酶活性被吸附到细胞上,而用相同量的抗卵清蛋白抗体包被的细胞仅吸附约10%的活性。NADH - 细胞色素c还原酶和醛脱氢酶活性被吸附到细胞上的程度与NADPH - 细胞色素c还原酶活性相同。在这种条件下,溶酶体和高尔基体的标记酶活性没有被吸附,而大量的质膜酶活性被吸附。微粒体组分中被吸附囊泡内NADPH - 细胞色素c还原酶的比活性显著增加。相反,高尔基体或质膜的标记酶可以在高尔基体组分未被吸附的囊泡中富集。