Home LiteratureArticle Details
PMID: 1940792 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Enhanced binding of peptide antigen to purified class II major histocompatibility glycoproteins at acidic pH.

The Journal of experimental medicine ·Vol. 174 ·No. 5 ·1991-11-01 ·Pages 1111-20

Jensen PE

Abstract

Helper T lymphocytes recognize peptide antigens stably associated with class II major histocompatibility complex (MHC) glycoproteins on the surface of antigen-presenting cells and serve to regulate a wide variety of immune responses. A previous study from our laboratory had demonstrated that the functional association of various peptide antigens with the antigen-presenting cell membrane was increased at pH 5 as compared to pH 7, consistent with the potential role of acidic endosomal compartments in antigen processing. The mechanism for this effect was not determined. In the present study, assays using purified class II glycoprotein were used to further define this mechanism. The potential requirement for pH-dependent interactions involving non-MHC membrane components was excluded in functional assays with purified class II reconstituted in artificial membranes containing only neutral phospholipids and cholesterol. The association of HEL(104-120) with I-Ed, and OVA(323-339) with I-Ad, was increased at pH 5, as measured by activation of specific T cell hybridomas. An enzyme immunoassay was developed to measure the binding of biotin-labeled peptides to purified class II in detergent micelles. The pH dependence of binding paralleled our previous functional results. Optimum binding of biotin-HEL(104-120) to I-Ed was observed at pH approximately 4.5, whereas maximum binding of biotin-Myo(106-118) to I-Ad occurred at pH approximately 5.5. The latter peptide also bound weakly to I-Ed, but with a pH dependence similar to that observed using HEL(104-120). Further experiments with biotin-HEL(104-120)/I-Ed indicated that both the apparent affinity and the apparent concentration of peptide-binding sites are increased as hydrogen ion concentration is increased from pH 7 to pH 5. The effect of pH in this range was largely reversible and was not associated with a change in peptide dissociation that could be measured with our assay system. Binding was not inhibited in the presence of 1.5 M NaCl, suggesting that electrostatic interactions between HEL(104-120) and I-Ed are not essential for binding. It is proposed that protonation of a critical group(s) in the class II molecule regulates its capacity to form stable complexes with peptide. However, this effect alone does not fully account for the rapid kinetics of peptide binding observed in experiments with intact antigen-presenting cells.

MeSH Terms
Amino Acid Sequence Animals Antigen-Presenting Cells/physiology Antigens/metabolism Biotin/metabolism Glycoproteins/metabolism Histocompatibility Antigens Class II/metabolism Hydrogen-Ion Concentration Immunoassay Mice Molecular Sequence Data Peptides/metabolism
Chemicals
Antigens Glycoproteins Histocompatibility Antigens Class II Peptides Biotin
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Jensen P E
Department of Pathology, Emory University School of Medicine, Atlanta, Georgia 30322.
References (34)
34 references, click to expand
  1. Mathematics of hormone-receptor interaction. I. Basic principles.
    Adv Exp Med Biol. 1973;36(0):289-326 PMID: 4368893
  2. T-cell antigenic peptides from sperm whale myoglobin fold as amphipathic helices: a possible determinant for immunodominance?
    Pept Res. 1989 Sep-Oct;2(5):314-21 PMID: 2520770
  3. Monoclonal antibodies to mouse MHC antigens. III. Hybridoma antibodies reacting to antigens of the H-2b haplotype reveal genetic control of isotype expression.
    J Immunol. 1981 Jan;126(1):317-21 PMID: 6935293
  4. Antigen-inducible, H-2-restricted, interleukin-2-producing T cell hybridomas. Lack of independent antigen and H-2 recognition.
    J Exp Med. 1981 May 1;153(5):1198-214 PMID: 6166712
  5. Studies on monoclonal antibodies to mouse MHC products.
    Transplant Proc. 1981 Mar;13(1 Pt 2):958-62 PMID: 6168076
  6. Quantitative analysis of drug-receptor interactions: I. Determination of kinetic and equilibrium properties.
    Life Sci. 1981 Jul 27;29(4):313-30 PMID: 6116136
  7. Decrease in macrophage antigen catabolism caused by ammonia and chloroquine is associated with inhibition of antigen presentation to T cells.
    Proc Natl Acad Sci U S A. 1982 Jan;79(1):175-8 PMID: 6798568
  8. Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing.
    J Exp Med. 1983 Aug 1;158(2):303-16 PMID: 6193218
  9. Processing of lysozyme by macrophages: identification of the determinant recognized by two T-cell hybridomas.
    Proc Natl Acad Sci U S A. 1984 Apr;81(8):2489-93 PMID: 6201858
  10. Segregation of transferrin to a mildly acidic (pH 6.5) para-Golgi compartment in the recycling pathway.
    Cell. 1984 Jul;37(3):789-800 PMID: 6204769
  11. Antigen recognition by H-2-restricted T cells. II. A tryptic ovalbumin peptide that substitutes for processed antigen.
    J Immunol. 1984 Oct;133(4):2067-74 PMID: 6332146
  12. The molecular basis of the requirement for antigen processing of pigeon cytochrome c prior to T cell activation.
    J Immunol. 1985 May;134(5):3233-40 PMID: 2580020
  13. Chloroquine affects biosynthesis of Ia molecules by inhibiting dissociation of invariant (gamma) chains from alpha-beta dimers in B cells.
    J Exp Med. 1985 Oct 1;162(4):1371-6 PMID: 3930653
  14. Binding of immunogenic peptides to Ia histocompatibility molecules.
    Nature. 1985 Sep 26-Oct 2;317(6035):359-61 PMID: 3876513
  15. Acidification of the endocytic and exocytic pathways.
    Annu Rev Biochem. 1986;55:663-700 PMID: 2874766
  16. Immunology. The ins and outs of antigen processing and presentation.
    Nature. 1986 Aug 21-27;322(6081):687-9 PMID: 3489186
  17. Isolation and characterization of antigen-Ia complexes involved in T cell recognition.
    Cell. 1986 Dec 26;47(6):1071-7 PMID: 3490919
  18. The relation between major histocompatibility complex (MHC) restriction and the capacity of Ia to bind immunogenic peptides.
    Science. 1987 Mar 13;235(4794):1353-8 PMID: 2435001
  19. Optimization of antigen presentation to T cell hybridomas by purified Ia molecules in planar membranes. Ia molecule polymorphism determines the antigenic fine specificity of the response to cytochrome c peptides.
    J Immunol Methods. 1987 Apr 2;98(1):29-41 PMID: 2435810
  20. Identification of a peptide binding protein that plays a role in antigen presentation.
    Proc Natl Acad Sci U S A. 1987 Mar;84(6):1659-63 PMID: 3031645
  21. High-resolution kinetics of transferrin acidification in BALB/c 3T3 cells: exposure to pH 6 followed by temperature-sensitive alkalinization during recycling.
    Proc Natl Acad Sci U S A. 1987 Oct;84(20):7119-23 PMID: 3478685
  22. Purification and characterization of class II histocompatibility antigens from a homozygous human B cell line.
    J Biol Chem. 1987 Nov 25;262(33):16087-94 PMID: 2824477
  23. Two distinct subpopulations of endosomes involved in membrane recycling and transport to lysosomes.
    Cell. 1988 Jan 15;52(1):73-83 PMID: 3345561
  24. Protein synthesis in antigen processing.
    J Immunol. 1988 Oct 15;141(8):2545-50 PMID: 3049813
  25. Autologous peptides constitutively occupy the antigen binding site on Ia.
    Science. 1988 Nov 18;242(4881):1045-7 PMID: 3194755
  26. Structural analysis of peptides capable of binding to more than one Ia antigen.
    J Immunol. 1989 Jan 1;142(1):35-40 PMID: 2535860
  27. A kinetic intermediate in the reaction of an antigenic peptide and I-Ek.
    Nature. 1989 Jan 19;337(6204):274-6 PMID: 2536141
  28. Acidification of endosome subpopulations in wild-type Chinese hamster ovary cells and temperature-sensitive acidification-defective mutants.
    J Cell Biol. 1989 Apr;108(4):1291-300 PMID: 2925786
  29. Stable association of processed antigen with antigen-presenting cell membranes.
    J Immunol. 1989 Jul 15;143(2):420-5 PMID: 2786907
  30. Minimum length of an idiotypic peptide and a model for its binding to a major histocompatibility complex class II molecule.
    EMBO J. 1989 Jul;8(7):1947-52 PMID: 2792076
  31. Characterization of a naturally processed MHC class II-restricted T-cell determinant of hen egg lysozyme.
    Nature. 1989 Dec 7;342(6250):682-4 PMID: 2480524
  32. Regulation of antigen presentation by acidic pH.
    J Exp Med. 1990 May 1;171(5):1779-84 PMID: 2332737
  33. The binary logic of antigen processing and presentation to T cells.
    Cell. 1990 Jul 27;62(2):203-6 PMID: 1695549
  34. Quantitative aspects of hormone-receptor interactions of high affinity. Effect of receptor concentration and measurement of dissociation constants of labeled and unlabeled hormones.
    Biochim Biophys Acta. 1975 Oct 6;406(2):294-303 PMID: 172127
Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1991-11-01
Pages
1111-20
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2118993
Subset
IM
Grants
NIAID NIH HHS · AI-30554 · United States
NCI NIH HHS · CA-46667 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]