M1 protein and protein H: IgGFc- and albumin-binding streptococcal surface proteins encoded by adjacent genes
- PMID: 8010973
- PMCID: PMC1138247
- DOI: 10.1042/bj3000877
M1 protein and protein H: IgGFc- and albumin-binding streptococcal surface proteins encoded by adjacent genes
Abstract
M1 protein and Protein H are surface proteins simultaneously present at the surface of certain strains of Streptococcus pyogenes, important pathogenic bacteria in humans. The present study concerns the structure, protein-binding properties and relationship between these two molecules. The gene encoding M1 protein (emm1) was found immediately upstream of the Protein H gene (sph). Both genes were preceded by a promoter region. Comparison of the sequences revealed a high degree of similarity in the signal peptides, the C repeats located in the central parts of the molecules and in the C-terminal cell-wall-attached regions, whereas the N-terminal sequences showed no significant similarity. Protein H has affinity for the Fc region of IgG antibodies. Also M1 protein, isolated from streptococcal culture supernatants or from Escherichia coli expressing emm1, was found to bind human IgGFc. When tested against polyclonal IgG from eight other mammalian species, M1 protein and Protein H both showed affinity for baboon, rabbit and pig IgG. M1 protein also reacted with guinea-pig IgG, whereas both streptococcal proteins were negative in binding experiments with rat, mouse, bovine and horse IgG. The two proteins were also tested against other members of the immunoglobulin super family: human IgM, IgA, IgD, IgE, beta 2-microglobulin, and major histocompatibility complex (MHC) class-I and class-II antigens. M1 protein showed no affinity for any of these molecules whereas Protein H reacted with MHC class-II antigens. M1 protein is known to bind albumin and fibrinogen also. The binding sites for these two plasma proteins and for IgGFc were mapped to different sites on M1 protein. Thus albumin bound to the C repeats and IgGFc to a region (S) immediately N-terminal of the C repeats. Finally, fibrinogen bound further towards the N-terminus but close to the IgGFc-binding site. On the fibrinogen molecule, fragment D was found to mediate binding to M1 protein. The IgGFc-binding region of M1 protein showed no similarity to that of Protein H. Still, competitive binding experiments demonstrated that the two streptococcal proteins bound to overlapping sites on IgGFc.
Similar articles
-
Antibody orientation at bacterial surfaces is related to invasive infection.J Exp Med. 2012 Dec 17;209(13):2367-81. doi: 10.1084/jem.20120325. Epub 2012 Dec 10. J Exp Med. 2012. PMID: 23230002 Free PMC article.
-
Protein H--a surface protein of Streptococcus pyogenes with separate binding sites for IgG and albumin.Mol Microbiol. 1994 Apr;12(1):143-51. doi: 10.1111/j.1365-2958.1994.tb01003.x. Mol Microbiol. 1994. PMID: 8057834
-
Human kininogens interact with M protein, a bacterial surface protein and virulence determinant.Biochem J. 1995 Jan 1;305 ( Pt 1)(Pt 1):173-80. doi: 10.1042/bj3050173. Biochem J. 1995. PMID: 7826326 Free PMC article.
-
IgA-specific proteins of pathogenic bacteria.Biochemistry (Mosc). 2009 Jan;74(1):12-21. doi: 10.1134/s0006297909010027. Biochemistry (Mosc). 2009. PMID: 19232043 Review.
-
[Fc-receptor proteins of Streptococcus pyogenes and pathogenesis of post-infection complications].Zh Mikrobiol Epidemiol Immunobiol. 2014 May-Jun;(3):78-90. Zh Mikrobiol Epidemiol Immunobiol. 2014. PMID: 25286515 Review. Russian.
Cited by
-
Plasma Protein Layer Concealment Protects Streptococcus pyogenes From Innate Immune Attack.Front Cell Infect Microbiol. 2021 May 20;11:633394. doi: 10.3389/fcimb.2021.633394. eCollection 2021. Front Cell Infect Microbiol. 2021. PMID: 34094995 Free PMC article.
-
Antibody orientation at bacterial surfaces is related to invasive infection.J Exp Med. 2012 Dec 17;209(13):2367-81. doi: 10.1084/jem.20120325. Epub 2012 Dec 10. J Exp Med. 2012. PMID: 23230002 Free PMC article.
-
Nanoscale binding site localization by molecular distance estimation on native cell surfaces using topological image averaging.Elife. 2022 Feb 24;11:e64709. doi: 10.7554/eLife.64709. Elife. 2022. PMID: 35200140 Free PMC article.
-
Streptococcus pyogenes evades adaptive immunity through specific IgG glycan hydrolysis.J Exp Med. 2019 Jul 1;216(7):1615-1629. doi: 10.1084/jem.20190293. Epub 2019 May 15. J Exp Med. 2019. PMID: 31092533 Free PMC article.
-
Greedy de novo motif discovery to construct motif repositories for bacterial proteomes.BMC Bioinformatics. 2019 Apr 18;20(Suppl 4):141. doi: 10.1186/s12859-019-2686-8. BMC Bioinformatics. 2019. PMID: 30999854 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous