Sherman I W, Jones L A
J Protozool. 1979 Aug;26(3):489-501. doi: 10.1111/j.1550-7408.1979.tb04659.x.
Plasma membranes of normal duckling erythrocytes were prepared by blender homogenization and nitro-en decompression. Surface membrane vesicles of red cells infected with the avian malaria Plasmodium lophurae were produced by nitrogen decompression. Membranes of erythrocyte-free malaria parasites were removed from cytoplasmic constituents by Dounce homogenization. These membranes were collected by centrifugation in a sucrose step gradient and purified on a linear sucrose gradient. Red cell membranes had a buoyant density of 1.159 g/cm3, whereas plasmodial membranes banded at 2 densities: 1.110 g/cm3 and 1.158 g/cm3. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of the isolated red cell membranes revealed 7 major protein bands with molecular weights (MW) ranging from 230, 000 to 22,000, and 3 glycoprotein bands with MW of 160,000, 88,000 and 37,000. Parasite membranes also had 7 major bands with MW ranging from 100,000 to 22,000. No glycoproteins were identifiable in these membranes. The proteins of the surface membranes from infected red cells had MW similar to those from normal red cells; however, there was some evidence of a reduction in the amount of the high MW polypeptides. The red cell membrane contained 79 nmoles sialic acid/mg membrane protein, whereas plasmodial membranes had 8 nmoles sialic acid/mg membrane protein. The sialic acid content of the surface membranes of infected red cells was significantly smaller than that of normal cells. Lactoperoxidase-glucose oxidase-catalyzed iodination of intact normal and malaria-infected erythrocytes labeled 7 surface components. Although no observable differences in iodinatable proteins were seen in these preparations, there was a striking reduction in the iodinatability of erythrocytic membranes obtained from P. lophurae-infected cells. Erythrocyte-free plasmodia bound very little radioactive iodine; the small amount of radioactivity was distributed among 3 major bands with MW of 42,000, 32,000 and 28,000. It is suggested that the alterations of the surface of the P. lophurae-infected erythrocyte do not occur by a wholesale insertion of plasmodial membrane proteins into the red cell plasma membrane, but rather that there are parasite-mediated modifications of existing membrane polypeptides.
通过搅拌器匀浆和氮气减压制备正常雏鸭红细胞的质膜。通过氮气减压制备感染禽疟原虫洛氏疟原虫的红细胞表面膜囊泡。通过杜恩斯匀浆从细胞质成分中去除无红细胞疟原虫的膜。这些膜通过在蔗糖阶梯梯度中离心收集,并在线性蔗糖梯度上纯化。红细胞膜的浮力密度为1.159 g/cm³,而疟原虫膜在两个密度处形成条带:1.110 g/cm³和1.158 g/cm³。对分离的红细胞膜进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,发现7条主要蛋白带,分子量(MW)范围为230,000至22,000,以及3条糖蛋白带,分子量分别为160,000、88,000和37,000。疟原虫膜也有7条主要带,分子量范围为100,000至22,000。在这些膜中未鉴定出糖蛋白。感染红细胞表面膜的蛋白质分子量与正常红细胞的相似;然而,有一些证据表明高分子量多肽的量减少。红细胞膜含有79 nmol唾液酸/mg膜蛋白,而疟原虫膜含有8 nmol唾液酸/mg膜蛋白。感染红细胞表面膜的唾液酸含量明显低于正常细胞。乳过氧化物酶-葡萄糖氧化酶催化完整的正常和感染疟疾的红细胞碘化,标记了7种表面成分。虽然在这些制剂中未观察到可碘化蛋白质的差异,但从感染洛氏疟原虫的细胞获得的红细胞膜的可碘化性显著降低。无红细胞疟原虫结合的放射性碘很少;少量放射性分布在分子量为42,000、32,000和28,000的3条主要带中。有人提出,感染洛氏疟原虫的红细胞表面的改变不是通过将疟原虫膜蛋白大量插入红细胞质膜而发生的,而是存在寄生虫介导的对现有膜多肽的修饰。