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Isolation and characterization of the plasma membrane of human erythrocytes infected with the malarial parasite Plasmodium falciparum.

机译:疟原虫恶性疟原虫感染的人红细胞质膜的分离和鉴定。

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摘要

Human erythrocytes infected with the malarial parasite Plasmodium falciparum were labeled metabolically with a mixture of 15 radioactive amino acids. When synchronously growing parasites were at the schizont stage of development infected cells were concentrated and purified by using a Percoll-Hypaque gradient. The plasma membrane of the infected erythrocyte, isolated by binding cells to a solid support (Affi-Gel 731, Bio-Rad), was less than 1% contaminated with parasite membranes. Erythrocyte membrane proteins were analyzed by polyacrylamide gel electrophoresis and autoradiography. Despite the high sensitivity of the procedure, there was no evidence for the insertion of parasite proteins into the infected host cell membrane. One possible exception is a Mr 230,000 parasite protein present maximally as 9,000 copies per infected erythrocyte membrane. Moreover, no differences in the membrane proteins were observed between a highly knobby clone and a knobless clone of the same strain of P. falciparum. These findings appear to rule out the presence of parasite protein(s) playing a structural role in the formation of knobs on the erythrocyte surface and question whether the antigenic determinants on the P. falciparum-infected erythrocyte are of parasite origin or whether such antigens represent newly exposed or chemically modified erythrocyte determinants.
机译:用15种放射性氨基酸的混合物在代谢上标记感染了疟原虫恶性疟原虫的人红细胞。当同步生长的寄生虫处于发育的裂殖体阶段时,将感染的细胞通过使用Percoll-Hypaque梯度进行浓缩和纯化。通过将细胞与固相支持物(Affi-Gel 731,Bio-Rad)结合而分离的被感染红细胞的质膜,被寄生虫膜污染的比例不到1%。通过聚丙烯酰胺凝胶电泳和放射自显影分析红细胞膜蛋白。尽管该方法具有很高的敏感性,但没有证据表明寄生虫蛋白会插入受感染的宿主细胞膜中。一个可能的例外是Mr 230,000寄生虫蛋白,每个被感染的红细胞膜最多存在9,000个拷贝。此外,在同一恶性疟原虫菌株的高度多节克隆和无节克隆之间未观察到膜蛋白的差异。这些发现似乎排除了寄生蛋白在红细胞表面纽结形成中起结构性作用的存在,并质疑恶性疟原虫感染的红细胞上的抗原决定簇是否是寄生虫起源的,或者这些抗原是否代表新近暴露或化学修饰的红细胞决定簇。

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  • 作者

    Gruenberg, J; Sherman, I W;

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  • 年度 1983
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  • 原文格式 PDF
  • 正文语种 en
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