Literature DB >> 8010973

M1 protein and protein H: IgGFc- and albumin-binding streptococcal surface proteins encoded by adjacent genes.

P Akesson1, K H Schmidt, J Cooney, L Björck.   

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.

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Year:  1994        PMID: 8010973      PMCID: PMC1138247          DOI: 10.1042/bj3000877

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  63 in total

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3.  Many group A streptococcal strains express two different immunoglobulin-binding proteins, encoded by closely linked genes: characterization of the proteins expressed by four strains of different M-type.

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Review 5.  Genetic manipulation of pathogenic streptococci.

Authors:  M G Caparon; J R Scott
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

6.  Protein H--a novel IgG binding bacterial protein.

Authors:  P Akesson; J Cooney; F Kishimoto; L Björck
Journal:  Mol Immunol       Date:  1990-06       Impact factor: 4.407

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Authors:  S E Holm; A Norrby; A M Bergholm; M Norgren
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Authors:  B N Manjula; K M Khandke; T Fairwell; W A Relf; K S Sriprakash
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9.  Nucleotide sequences of two adjacent M or M-like protein genes of group A streptococci: different RNA transcript levels and identification of a unique immunoglobulin A-binding protein.

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10.  FIBRINOGEN PRECIPITATION BY STREPTOCOCCAL M PROTEIN. I. IDENTITY OF THE REACTANTS, AND STOICHIOMETRY OF THE REACTION.

Authors:  F S KANTOR
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  58 in total

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3.  Expression of both M protein and hyaluronic acid capsule by group A streptococcal strains results in a high virulence for chicken embryos.

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6.  Characterization of group a streptococcal M23 protein and comparison of the M3 and M23 protein's ligand-binding domains.

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Review 7.  Variation, Indispensability, and Masking in the M protein.

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8.  Expression of the Arp protein, a member of the M protein family, is not sufficient to inhibit phagocytosis of Streptococcus pyogenes.

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9.  Functional dissection of Streptococcus pyogenes M5 protein: the hypervariable region is essential for virulence.

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10.  M protein from Streptococcus pyogenes induces tissue factor expression and pro-coagulant activity in human monocytes.

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