Reddy M S
Department of Oral Biology, School of Dental Medicine, State University of New York at Buffalo, Buffalo, NY 14214, USA.
Curr Microbiol. 1998 Dec;37(6):395-402. doi: 10.1007/s002849900399.
In previous experiments, we have shown that [125I]pili of Pseudomonas aeruginosa exhibited specific binding to a low-molecular-weight mucin (MG2) of human submandibular-sublingual saliva (HSMSL; Reddy MS, Levine MJ, Paranchych W. Crit Rev Oral Biol Med 4:315-323, 1993). In the present study, I have utilized unlabeled pili and immunostaining to identify the receptor molecules in HSMSL. In addition to MG2, pili also bound to neutral cystatin (CsnSN). Binding of unlabeled pili to MG2 and CsnSN could be abolished by treatment of HSMSL with trypsin to hydrolyze the peptide moieties or N-acetylation to neutralize the positive charges of the lysine residues. Reductive methylation of HSMSL, which modifies the lysine residues to methyl lysines while retaining the positive charges, did not affect the binding of pili to either MG2 or CsnSN. Further, pili also exhibited binding to a recombinant MG2 peptide (aa 1-86). Collectively, the data suggested that a protein-to-protein interaction via electrostatic forces mediates the binding of the pili to MG2 and CsnSN. Iodination of pili, which modifies tyrosine-24 and/or -27 residues to O-iodotyrosine(s), abolished its binding to CsnSN but not to MG2. These results suggested that the conformation of pili also plays a role in interaction with CsnSN. Conformational change(s) of pili induced by iodination also made it susceptible to hydrolysis with trypsin.
在之前的实验中,我们已表明铜绿假单胞菌的[125I]菌毛与人颌下-舌下唾液(HSMSL)中的一种低分子量粘蛋白(MG2)呈现特异性结合(Reddy MS、Levine MJ、Paranchych W。《口腔生物学与医学评论》4:315 - 323,1993年)。在本研究中,我利用未标记的菌毛和免疫染色来鉴定HSMSL中的受体分子。除了MG2,菌毛还与中性半胱氨酸蛋白酶抑制剂(CsnSN)结合。用胰蛋白酶处理HSMSL以水解肽部分或进行N - 乙酰化以中和赖氨酸残基的正电荷,可消除未标记菌毛与MG2和CsnSN的结合。HSMSL 的还原甲基化将赖氨酸残基修饰为甲基赖氨酸,同时保留正电荷,这并不影响菌毛与MG2或CsnSN的结合。此外,菌毛还与重组MG2肽(氨基酸1 - 86)表现出结合。总体而言,数据表明通过静电力的蛋白质 - 蛋白质相互作用介导了菌毛与MG2和CsnSN的结合。菌毛的碘化将酪氨酸 - 24和/或 - 27残基修饰为O - 碘酪氨酸,消除了其与CsnSN的结合,但未消除与MG2的结合。这些结果表明菌毛的构象在与CsnSN的相互作用中也起作用。碘化诱导的菌毛构象变化也使其易于被胰蛋白酶水解。