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恶性疟原虫裂殖子与人类红细胞相互作用的生化基础研究。

Studies on the biochemical basis of the interaction of the merozoites of Plasmodium falciparum and the human red cell.

作者信息

Jungery M

出版信息

Trans R Soc Trop Med Hyg. 1985;79(5):591-7. doi: 10.1016/0035-9203(85)90164-6.

Abstract

The red cell membrane appears to possess receptors for malarial parasites which are species specific. Plasmodium falciparum invades red cells that have the surface sialoglycoproteins, glycophorins A, B and C. Several regions of these molecules are critical to parasite binding. Invasion of red cells by merozoites can be blocked by both antibodies directed to specific sites on glycophorin and tryptic fragments of these molecules. The parasites appear to bind to the red cells in a lectin-like fashion, since three monosaccharides, namely N-acetyl-glucosamine (Glu NAc), N-acetyl-galactosamine (Gal NAc) and N-acetyl-neuraminic acid (Neu NAc), can specifically block parasite invasion in vitro. Neoglycoproteins made by coupling these sugars to BSA are particularly effective. Possible mechanisms of parasite attachment to and invasion of red cells are discussed.

摘要

红细胞膜似乎拥有疟原虫的受体,这些受体具有物种特异性。恶性疟原虫侵入具有表面唾液糖蛋白、血型糖蛋白A、B和C的红细胞。这些分子的几个区域对寄生虫结合至关重要。裂殖子对红细胞的侵入可被针对血型糖蛋白上特定位点的抗体以及这些分子的胰蛋白酶片段所阻断。寄生虫似乎以凝集素样方式与红细胞结合,因为三种单糖,即N-乙酰葡糖胺(GlcNAc)、N-乙酰半乳糖胺(GalNAc)和N-乙酰神经氨酸(NeuNAc),可以在体外特异性阻断寄生虫的侵入。通过将这些糖与牛血清白蛋白偶联制成的新糖蛋白特别有效。文中讨论了寄生虫附着和侵入红细胞的可能机制。

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