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Effects of Surface Proteins of Human Erythrocyte Membrane on the Interaction with Lipopolysaccharidesfrom Escherichia coli 055:B5

机译:人红细胞膜表面蛋白对与大肠杆菌055:B5脂多糖相互作用的影响

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摘要

The role of erythrocytic surface membrane proteins and membrane charge in the interactions of theerythrocytes with lipopolysaccharides (LPS) isolated from Escherichia coli 055:B5 (LPS-(E.coli),S-form) hasbeen examined by two independent methods, flow cytometry and cell electrophoresis. Treatment of erythro-cytes with trypsin that modifies stereochemical properties of cell surface resulted in a 16% increase in the levelof the erythrocyte fluorescence measured after their incubation with fluorescently labeled LPS_(E.coli).Electro-phoretic mobility (EM) of the trypsin-treated erythrocytes was reduced by 16%. The removal of sialic acidsfrom the erythrocyte surface with neuraminidase had no considerable effect either on the relative EM values orfluorescence intensity after the incubation of cells with LPS. The results suggest that the major role in the incor-poration of the S-form LPS into the membrane of human erythrocytes is played by stereochemical factors,whereas the cell surface charge is less significant.
机译:红细胞表面膜蛋白和膜电荷在红细胞与分离自大肠杆菌055:B5的脂多糖(LPS-(E.coli),S-form)相互作用中的作用已通过两种独立的方法进行了研究:流式细胞术和细胞电泳。用胰蛋白酶处理红细胞可以改变细胞表面的立体化学特性,使它们与荧光标记的LPS_(E.coli)孵育后测得的红细胞荧光水平增加了16%。胰蛋白酶的电泳迁移率(EM)经处理的红细胞减少了16%。用神经氨酸酶从红细胞表面去除唾液酸对LPS孵育细胞后的相对EM值或荧光强度均无显着影响。结果表明,立体化学因素在S型脂多糖掺入人红细胞膜中起主要作用,而细胞表面电荷的重要性较低。

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