Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1978 Jun 1;147(6):1771–1778. doi: 10.1084/jem.147.6.1771

Streptococcal M protein extracted by nonionic detergent. III. Correlation between immunological cross-reactions and structural similarities with implications for antiphagocytosis

PMCID: PMC2184311  PMID: 355596

Abstract

Three immunologically cross-reactive and non-cross-reactive streptococcal M proteins were analyzed by a chromatographic tryptic peptide mapping system. The results indicate that cross-reactions correlate with the extent of structural similarity among the M protein molecules analyzed. The data also reveal that free lysine is released by the action of trypsin from these three M proteins, suggesting a common lys-lys or arg-lys sequence. In addition, only one peptide has been found to be common within all three M types. This limited structural relatedness among the three M proteins examined indicates that sequence variation plays a major role in the immunological specificity of the M antigens. However, despite sequence variation, all M protein molecules have a common antiphagocytic activity. The fact that no common opsonic antibody has yet been found, even against limited M types, argues against this biological activity being solely the result of a common sequence. Based on these data, it is suggested that the antiphagocytic effect of M protein may be due to a conformationally created environment on the surface of the molecule which is selected by both immunological and biological pressure.

Full Text

The Full Text of this article is available as a PDF (524.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Atassi M. Z., Habeeb A. F., Rydstedt L. Lack of immunochemical cross-reaction between lysozyme and alpha-lactalbumin and comparison of their conformations. Biochim Biophys Acta. 1970 Jan 20;200(1):184–187. doi: 10.1016/0005-2795(70)90061-9. [DOI] [PubMed] [Google Scholar]
  2. Atassi M. Z., Saplin B. J. Immunochemistry of sperm whale myoglobin. X. Regions responsible for immunochemical cross-reaction with finback whale myoglobin. Some general conclusions concerning immunochemical cross-reaction of proteins. Biochemistry. 1971 Dec 7;10(25):4740–4747. doi: 10.1021/bi00801a021. [DOI] [PubMed] [Google Scholar]
  3. Atassi M. Z., Tarlowski D. P., Paull J. H. Immunochemistry of sperm whale myoglobin. VII. Correlation of immunochemical cross-reaction of eight myoglobins with structural similarity and its dependence on conformation. Biochim Biophys Acta. 1970 Dec 22;221(3):623–635. doi: 10.1016/0005-2795(70)90234-5. [DOI] [PubMed] [Google Scholar]
  4. Beachey E. H., Stollerman G. H., Chiang E. Y., Chiang T. M., Seyer J. M., Kang A. H. Purification and properties of M protein extracted from group A streptococci with pepsin: covalent structure of the amino terminal region of type 24 M antigen. J Exp Med. 1977 Jun 1;145(6):1469–1483. doi: 10.1084/jem.145.6.1469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bergner-Rabinowitz S., Ofek I., Moody M. D. Cross-protection among serotypes of group A streptococci. J Infect Dis. 1972 Apr;125(4):339–344. doi: 10.1093/infdis/125.4.339. [DOI] [PubMed] [Google Scholar]
  6. Brew K., Campbell P. N. The characterization of the whey proteins of guinea-pig milk. The isolation and properties of alpha-lactalbumin. Biochem J. 1967 Jan;102(1):258–264. doi: 10.1042/bj1020258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Brew K., Vanaman T. C., Hill R. L. Comparison of the amino acid sequence of bovine alpha-lactalbumin and hens egg white lysozyme. J Biol Chem. 1967 Aug 25;242(16):3747–3749. [PubMed] [Google Scholar]
  8. Fischetti V. A., Gotschlich E. C., Siviglia G., Zabriskie J. B. Streptococcal M protein extracted by nonionic detergent. I. Properties of the antiphagocytic and type-specific molecules. J Exp Med. 1976 Jul 1;144(1):32–53. doi: 10.1084/jem.144.1.32. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fischetti V. A. Streptococcal M protein extracted by nonionic detergent. II. Analysis of the antibody response to the multiple antigenic determinants of the M-protein molecule. J Exp Med. 1977 Oct 1;146(4):1108–1123. doi: 10.1084/jem.146.4.1108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fox E. N., Wittner M. K. Antigenicity of the M proteins of group A hemolytic streptococci. IV. Cross-reactivity between serotypes. J Immunol. 1968 Jan;100(1):39–45. [PubMed] [Google Scholar]
  11. Fox E. N., Wittner M. K. New observations on the structure and antigenicity of the M proteins of the group A streptococcus. Immunochemistry. 1969 Jan;6(1):11–24. doi: 10.1016/0019-2791(69)90174-8. [DOI] [PubMed] [Google Scholar]
  12. Kronman M. J. Similarity in backbone conformation of egg white lysozyme and bovine gamma lactalbumin. Biochem Biophys Res Commun. 1968 Nov 25;33(4):535–541. doi: 10.1016/0006-291x(68)90327-6. [DOI] [PubMed] [Google Scholar]
  13. LANCEFIELD R. C. Differentiation of group A streptococci with a common R antigen into three serological types, with special reference to the bactericidal test. J Exp Med. 1957 Oct 1;106(4):525–544. doi: 10.1084/jem.106.4.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lee C. L., Atassi M. Z. Delineation of the third antigenic site of lysozyme by application of a novel 'surface-simulation' synthetic approach directly linking the conformationally adjacent residues forming the site. Biochem J. 1976 Oct 1;159(1):89–93. doi: 10.1042/bj1590089. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Myoda T. T., Wiley G. G., Bruno P. N. Cross-reactions among group A streptococci. IV. Extraction, separation and purification of two protective antigens of type G 1 cocci. J Immunol. 1973 Jul;111(1):249–259. [PubMed] [Google Scholar]
  16. Schwabe C., Catlin J. C. Removal of a Fluoram 1-positive impurity from hydrochloric acid. Anal Biochem. 1974 Sep;61(1):302–304. doi: 10.1016/0003-2697(74)90361-3. [DOI] [PubMed] [Google Scholar]
  17. Wiley G. G., Bruno P. N. Cross-reactions among Group A streptococci. I. Precipitin and bactericidal cross-reactions among types 33, 41, 43, 52, and Ross. J Exp Med. 1968 Nov 1;128(5):959–968. doi: 10.1084/jem.128.5.959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Wiley G. G., Bruno P. N. Cross-reactions among group A streptococci. II. Further analysis of antigens related to type-specificity and protection. J Immunol. 1969 Aug;103(2):149–154. [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES