Marceau M, Forest K, Béretti J L, Tainer J, Nassif X
INSERM U411, Laboratoire de Microbiologie, Faculté de Médecine Necker-Enfants Malades, Paris, France.
Mol Microbiol. 1998 Feb;27(4):705-15. doi: 10.1046/j.1365-2958.1998.00706.x.
Pili, which are assembled from protein subunits called pilin, are indispensable for the adhesion of capsulated Neisseria meningitidis (MC) to eukaryotic cells. Both MC and Neisseria gonorrhoeae (GC) pilins are glycosylated, but the effect of this modification is unknown. In GC, a galactose alpha-1,3-N-acetyl glucosamine is O-linked to Ser-63, whereas in MC, an O-linked trisaccharide is present between residues 45 and 73 of pilin. As Ser-63 was found to be conserved in pilin variants from different strains, it was replaced by Ala in two MC variants to test the possible role of this residue in pilin glycosylation and modulation of pili function. The mutated alleles were stably expressed in MC, and the proteins they encoded migrated more quickly than the normal protein during SDS-PAGE. As controls, neighbouring Asn-61 and Ser-62 were replaced by an Ala with no effect on electrophoretic mobility. Silver staining of purified pilin obtained from MC after oxidation with periodic acid confirmed the loss of glycosylation in the Ser-63-->Ala pilin variants. Mass spectrometry of HPLC-purified trypsin-digested peptides of pilin and Ser-63-->Ala pilin confirmed that peptide 45-73 has the molecular size of a glycopeptide in the wild type. In strains producing non-glycosylated pilin variants, we observed that (i) no truncated S pilin monomer was produced; (ii) piliation was slightly increased; and (iii) presumably as a consequence, adhesiveness for epithelial cells was increased 1.6- to twofold in these derivatives. In addition, pilin monomers and/or individual pilus fibres, obtained after solubilization of a crude pili preparation in a high pH buffer, were reassociated into insoluble aggregates of pili more completely with non-glycosylated variants than with the normal pilin. Taken together, these data eliminate a major role for pilin glycosylation in piliation and subsequent pilus-mediated adhesion, but they demonstrate that glycosylation facilitates solubilization of pilin monomers and/or individual pilus fibres.
菌毛由称为菌毛蛋白的蛋白质亚基组装而成,对于荚膜脑膜炎奈瑟菌(MC)黏附真核细胞而言不可或缺。MC和淋病奈瑟菌(GC)的菌毛蛋白都进行了糖基化修饰,但这种修饰的作用尚不清楚。在GC中,一个半乳糖α-1,3-N-乙酰葡糖胺以O-连接的方式连接到Ser-63上,而在MC中,一个O-连接的三糖存在于菌毛蛋白45至73位残基之间。由于发现Ser-63在不同菌株的菌毛蛋白变体中是保守的,因此在两个MC变体中将其替换为Ala,以测试该残基在菌毛蛋白糖基化和菌毛功能调节中的可能作用。突变等位基因在MC中稳定表达,它们编码的蛋白质在SDS-PAGE期间迁移速度比正常蛋白质更快。作为对照,相邻的Asn-61和Ser-62被替换为Ala,对电泳迁移率没有影响。用高碘酸氧化后从MC获得的纯化菌毛蛋白的银染证实了Ser-63→Ala菌毛蛋白变体中糖基化的丧失。对菌毛蛋白和Ser-63→Ala菌毛蛋白经HPLC纯化的胰蛋白酶消化肽段进行质谱分析,证实野生型中45-73肽段具有糖肽的分子大小。在产生非糖基化菌毛蛋白变体的菌株中,我们观察到:(i)没有产生截短的S菌毛蛋白单体;(ii)菌毛形成略有增加;(iii)大概因此,这些衍生物对上皮细胞的黏附性增加了1.6至两倍。此外,在高pH缓冲液中溶解粗菌毛制剂后获得的菌毛蛋白单体和/或单个菌毛纤维,与非糖基化变体相比,与正常菌毛蛋白更完全地重新缔合成不溶性菌毛聚集体。综上所述,这些数据排除了菌毛蛋白糖基化在菌毛形成和随后的菌毛介导黏附中的主要作用,但它们表明糖基化促进了菌毛蛋白单体和/或单个菌毛纤维的溶解。