Glasgow L R, Hill R L
Infect Immun. 1980 Nov;30(2):353-61. doi: 10.1128/iai.30.2.353-361.1980.
The binding of several glycoproteins to freshly grown and harvested cells of Mycoplasma gallisepticum was examined. Only human glycophorin, the major sialoglycoprotein of the erythrocyte membrane, bound tightly as judged by direct binding assays with 125I-labeled glycoproteins. Neuraminidase-treated glycophorin did not bind, suggesting that binding is mediated through sialic acid groups. Although other sialoglycoproteins did not appear to bind M. gallisepticum by direct binding assays, some inhibited the binding of glycophorin. The best inhibitors had a mucin-like structure, with high molecular weights and high sialic acid contents. N-acetylneuraminic acid appeared to be the favored sialic acid structure for binding, but there was no strict specificity for its anomeric linkage. Neuraminidase activity could not be detected on the surface of M. gallisepticum, suggesting that this enzyme is not involved in the mechanism of adherence of sialoglycoproteins. Binding of sialoglycoproteins was time dependent, however, and markedly diminished with increasing ionic strength, but was largely unaffected between pH 4 and 9.
对几种糖蛋白与新鲜培养及收获的鸡毒支原体细胞的结合情况进行了检测。通过用¹²⁵I标记的糖蛋白进行直接结合试验判断,只有人血型糖蛋白(红细胞膜的主要唾液酸糖蛋白)紧密结合。经神经氨酸酶处理的血型糖蛋白不结合,这表明结合是通过唾液酸基团介导的。尽管通过直接结合试验其他唾液酸糖蛋白似乎不与鸡毒支原体结合,但有些能抑制血型糖蛋白的结合。最佳抑制剂具有类黏蛋白结构,分子量高且唾液酸含量高。N - 乙酰神经氨酸似乎是结合时最有利的唾液酸结构,但其异头碳连接没有严格的特异性。在鸡毒支原体表面未检测到神经氨酸酶活性,这表明该酶不参与唾液酸糖蛋白的黏附机制。然而,唾液酸糖蛋白的结合具有时间依赖性,并且随着离子强度增加而显著减少,但在pH 4至9之间基本不受影响。