Ruangjirachuporn W, Udomsangpetch R, Carlsson J, Drenckhahn D, Perlmann P, Berzins K
Department of Immunology, Stockholm University, Sweden.
Exp Parasitol. 1991 Jul;73(1):62-72. doi: 10.1016/0014-4894(91)90008-k.
The location of the Plasmodium falciparum vaccine candidate antigen Pf155/RESA in the membrane of infected erythrocytes was analzyed by means of selective surface radioiodination and immunofluorescence of surface-modified cells. The lack of radiolabel in Pf155/RESA as well as its localization by immunofluorescence similar to that of the N-terminal region of erythrocyte band 3 suggests that the antigen is associated with the cytoplasmic phase of the erythrocyte membrane. In concordance with this, Pf155/RESA was detected by immunofluorescence on the surface of inside out membrane vesicles from P. falciparum-infected erythrocytes. Pf155/RESA from spent culture medium also bound to inside out membrane vesicles of normal erythrocytes as well as to cytoskeletal shells of such vesicles, but failed to bind to sealed right-side out membrane vesicles. Depletion of spectrin from the vesicles abolished antigen binding, suggesting that Pf155/RESA association with the erythrocyte cytoskeleton is mediated by spectrin.
通过选择性表面放射性碘化和表面修饰细胞的免疫荧光分析,研究了恶性疟原虫疫苗候选抗原Pf155/RESA在受感染红细胞膜中的定位。Pf155/RESA缺乏放射性标记,且其免疫荧光定位类似于红细胞带3的N端区域,这表明该抗原与红细胞膜的细胞质相相关。与此一致的是,在恶性疟原虫感染红细胞的外翻膜囊泡表面通过免疫荧光检测到了Pf155/RESA。来自用过的培养基中的Pf155/RESA也与正常红细胞的外翻膜囊泡以及此类囊泡的细胞骨架壳结合,但未能与密封的外翻膜囊泡结合。从囊泡中去除血影蛋白消除了抗原结合,这表明Pf155/RESA与红细胞细胞骨架的结合是由血影蛋白介导的。