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. 1982 Sep;79(17):5388–5391. doi: 10.1073/pnas.79.17.5388

Isolation and identification of a biologically active peptide derived from the CH3 domain of human IgG1.

E L Morgan, T E Hugli, W O Weigle
PMCID: PMC346902  PMID: 6215650

Abstract

A 24-amino acid residue peptide has been isolated from the Fc region of a human IgG1 myeloma protein. The peptide has associated with it the same ability to induce murine B cells to polyclonally secrete antibody as does the intact Fc fragment. Amino acid composition of the peptide indicates that on a mole/mole basis the isolated peptide is identical to that published for residues 335-358 in the Eu IgG1 sequence. This peptide corresponds roughly to the first 24 amino acids of the CH3 domain. It is believed that the immunoregulatory properties that have been ascribed to the Fc fragment are associated with this peptide.

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Selected References

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

  1. Barnett Foster D. E., Dorrington K. J., Painter R. H. Structure and function of immunoglobulin domains. VII. Studies on the structural requirements of human immunoglobulin G for granulocyte binding. J Immunol. 1978 Jun;120(6):1952–1956. [PubMed] [Google Scholar]
  2. Barnett-Foster D. E., Painter R. H. The interaction of the Facb fragment of rabbit anti-sheep red cell IgG with guinea pig macrophages, and human monocytes and granulocytes. Mol Immunol. 1982 Feb;19(2):247–252. doi: 10.1016/0161-5890(82)90337-6. [DOI] [PubMed] [Google Scholar]
  3. Ciccimarra F., Rosen F. S., Merler E. Localization of the IgG effector site for monocyte receptors. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2081–2083. doi: 10.1073/pnas.72.6.2081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Connell G. E., Painter R. H. Fragmentation of immunoglobulin during storage. Can J Biochem. 1966 Mar;44(3):371–379. doi: 10.1139/o66-044. [DOI] [PubMed] [Google Scholar]
  5. Edelman G. M., Cunningham B. A., Gall W. E., Gottlieb P. D., Rutishauser U., Waxdal M. J. The covalent structure of an entire gammaG immunoglobulin molecule. Proc Natl Acad Sci U S A. 1969 May;63(1):78–85. doi: 10.1073/pnas.63.1.78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Jerne N. K., Nordin A. A. Plaque Formation in Agar by Single Antibody-Producing Cells. Science. 1963 Apr 26;140(3565):405–405. doi: 10.1126/science.140.3565.405. [DOI] [PubMed] [Google Scholar]
  7. Kettman J., Dutton R. W. An in vitro primary immune response to 2,4,6-trinitrophenyl substituted erythrocytes: response against carrier and hapten. J Immunol. 1970 Jun;104(6):1558–1561. [PubMed] [Google Scholar]
  8. Klein M., Neauport-Sautes C., Ellerson J. R., Fridman W. H. Binding site of human IgG subclasses and their domains for Fc receptors of activated murine T cells. J Immunol. 1977 Sep;119(3):1077–1083. [PubMed] [Google Scholar]
  9. Michaelsen T. E., Wisloff F., Natvig J. B. Structural requirements in the Fc region of rabbit IgG antibodies necessary to induce cytotoxicity by human lymphocytes. Scand J Immunol. 1975;4(1):71–78. doi: 10.1111/j.1365-3083.1975.tb02601.x. [DOI] [PubMed] [Google Scholar]
  10. Morgan E. L., Thoman M. L., Walker S. M., Weigle W. O. Regulation of the immune response. II. Characterization of the cell population(s) involved in the Fc fragment-induced adjuvant effect. J Immunol. 1980 Sep;125(3):1275–1279. [PubMed] [Google Scholar]
  11. Morgan E. L., Thoman M. L., Weigle W. O. Enhancement of T lymphocyte functions by Fc fragments of immunoglobulins. I. Augmentation of allogeneic mixed lymphocyte culture reactions requires I-A- or I-B-subregion differences between effector and stimulator cell populations. J Exp Med. 1981 May 1;153(5):1161–1172. doi: 10.1084/jem.153.5.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Morgan E. L., Thoman M. L., Weigle W. O. Enhancement of T. lymphocyte functions by Fc fragments of immunoglobulin. II. Augmentation of the cell-mediated lympholysis response occurs through an Lyt-1+2- helper T cell. J Immunol. 1981 Dec;127(6):2526–2530. [PubMed] [Google Scholar]
  13. Morgan E. L., Walker S. M., Thoman M. L., Weigle W. O. Regulation of the immune response. I. The potentiation of in vivo and in vitro immune responses by Fc fragments. J Exp Med. 1980 Jul 1;152(1):113–123. doi: 10.1084/jem.152.1.113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Morgan E. L., Weigle W. O. Aggregated human gamma-globulin-induced proliferation and polyclonal activation of murine B lymphocytes. J Immunol. 1980 Jul;125(1):226–231. [PubMed] [Google Scholar]
  15. Morgan E. L., Weigle W. O. Polyclonal activation of human B lymphocytes by Fc fragments. I. Characterization of the cellular requirements for Fc fragment-mediated polyclonal antibody secretion by human peripheral blood B lymphocytes. J Exp Med. 1981 Sep 1;154(3):778–790. doi: 10.1084/jem.154.3.778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Morgan E. L., Weigle W. O. Polyclonal activation of murine B lymphocytes by Fc fragments. I. The requirement for two signals in the generation of the polyclonal antibody response induced by Fc fragments. J Immunol. 1980 Mar;124(3):1330–1335. [PubMed] [Google Scholar]
  17. Morgan E. L., Weigle W. O. Regulation of B lymphocyte activation by the Fc portion of immunoglobulin. J Supramol Struct. 1980;14(2):201–208. doi: 10.1002/jss.400140208. [DOI] [PubMed] [Google Scholar]
  18. Morgan E. L., Weigle W. O. Regulation of Fc fragment-induced murine spleen cell proliferation. J Exp Med. 1980 Jan 1;151(1):1–11. doi: 10.1084/jem.151.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Morgan E. L., Weigle W. O. The requirement for adherent cells in the Fc fragment-induced proliferative response of murine spleen cells. J Exp Med. 1979 Aug 1;150(2):256–266. doi: 10.1084/jem.150.2.256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Natvig J. B., Kunkel H. G. Human immunoglobulins: classes, subclasses, genetic variants, and idiotypes. Adv Immunol. 1973;16:1–59. doi: 10.1016/s0065-2776(08)60295-3. [DOI] [PubMed] [Google Scholar]
  21. PORTER R. R. The hydrolysis of rabbit y-globulin and antibodies with crystalline papain. Biochem J. 1959 Sep;73:119–126. doi: 10.1042/bj0730119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Thoman M. L., Morgan E. L., Weigle W. O. Activation of T lymphocytes by the Fc portion of immunoglobulin. J Supramol Struct. 1980;13(4):479–488. doi: 10.1002/jss.400130407. [DOI] [PubMed] [Google Scholar]
  23. Thoman M. L., Morgan E. L., Weigle W. O. Fc fragment activation of T lymphocytes. I. Fc fragments trigger Lyt 1+23- T lymphocytes to release a helper T cell-replacing activity. J Immunol. 1981 Feb;126(2):632–635. [PubMed] [Google Scholar]
  24. Thoman M. L., Morgan E. L., Weigle W. O. Polyclonal activation of murine B lymphocytes by Fe fragments. II. Replacement of T cells by a soluble helper T cell-replacing factor (TRF). J Immunol. 1980 Oct;125(4):1630–1633. [PubMed] [Google Scholar]
  25. Waxdal M. J., Konigsberg W. H., Henley W. L., Edelman G. M. The covalent structure of a human gamma G-immunoglobulin. II. Isolation and characterization of the cyanogen bromide fragments. Biochemistry. 1968 May;7(5):1959–1966. doi: 10.1021/bi00845a046. [DOI] [PubMed] [Google Scholar]
  26. Yasmeen D., Ellerson J. R., Dorrington K. J., Painter R. H. Evidence for the domain hypothesis: location of the site of cytophilic activity toward guinea pig macrophages in the C H 3 homology region of human immunoglobulin G. J Immunol. 1973 Jun;110(6):1706–1709. [PubMed] [Google Scholar]

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