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在富含诺氏疟原虫感染红细胞表面膜的膜制剂中鉴定寄生虫蛋白。

Identification of parasite proteins in a membrane preparation enriched for the surface membrane of erythrocytes infected with Plasmodium knowlesi.

作者信息

Aley S B, Barnwell J W, Daniel W, Howard R J

出版信息

Mol Biochem Parasitol. 1984 May;12(1):69-84. doi: 10.1016/0166-6851(84)90045-8.

Abstract

A subcellular fraction enriched in erythrocyte membranes has been isolated from rhesus monkey erythrocytes infected with Plasmodium knowlesi. Infected cells were lysed by centrifugation through a zone of hypotonic buffer and membranes isolated by equilibrium density gradient centrifugation in the same tube. The purified membrane fraction was shown to include the erythrocyte surface membrane by several methods: electron microscopy, identification of Coomassie Blue stained erythrocyte membrane proteins, identification of band 3 with a monoclonal antibody, and identification of radioiodinated cell surface proteins. The resulting ghosts were shown to be specifically reactive with monkey sera against the variant surface antigens of P. knowlesi by indirect immunofluorescence and membrane agglutination. No reactivity was seen with a monoclonal antibody (13C11) against the intracellular schizont surface. A number of metabolically labelled parasite proteins were enriched in this membrane function, including peptides of 277, 208, 173, 153, 134, 109, 80, 60 and 48 kDa and the variant surface antigens of variable molecular mass (180-207 kDa). These proteins were distinct from the major parasite proteins of total infected erythrocytes and isolated merozoites. The major glucosamine labelled glycoprotein of the internal schizont (230 kDa) was not found in this fraction. Moreover, no fragment of this parasite glycoprotein was found in this membrane fraction, indicating that no part of this molecule is transported to the erythrocyte surface. In contrast, the variant antigen of P. knowlesi, known to be on the erythrocyte surface, could be readily identified as peptides unique to specific cloned parasite lines. We propose that the other nine parasite proteins found within this membrane fraction represent a starting point for the identification of other parasite proteins transported to the surface membrane of the infected erythrocyte.

摘要

已从感染诺氏疟原虫的恒河猴红细胞中分离出富含红细胞膜的亚细胞组分。通过在低渗缓冲液区域进行离心使感染细胞裂解,并在同一管中通过平衡密度梯度离心分离膜。通过几种方法证明纯化的膜组分包括红细胞表面膜:电子显微镜、考马斯亮蓝染色的红细胞膜蛋白鉴定、用单克隆抗体鉴定带3以及放射性碘化细胞表面蛋白鉴定。通过间接免疫荧光和膜凝集显示,所得的血影与抗诺氏疟原虫可变表面抗原的猴血清具有特异性反应。针对细胞内裂殖体表面的单克隆抗体(13C11)未观察到反应性。许多经代谢标记的寄生虫蛋白在该膜组分中富集,包括277、208、173、153、134、109、80、60和48 kDa的肽以及可变分子量(180 - 207 kDa)的可变表面抗原。这些蛋白与总感染红细胞和分离的裂殖子中的主要寄生虫蛋白不同。在该组分中未发现内部裂殖体的主要氨基葡萄糖标记糖蛋白(230 kDa)。此外,在该膜组分中未发现该寄生虫糖蛋白的片段,表明该分子的任何部分都未转运至红细胞表面。相比之下,已知位于红细胞表面的诺氏疟原虫可变抗原可作为特定克隆寄生虫系特有的肽轻易鉴定出来。我们提出,在该膜组分中发现的其他九种寄生虫蛋白代表了鉴定转运至感染红细胞表面膜的其他寄生虫蛋白的起点。

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