A novel system for convenient detection of low‐affinity receptor–ligand interactions: Chelator‐lipid liposomes engrafted with recombinant CD4 bind to cells expressing MHC class II
- 1 June 2001
- journal article
- research article
- Published by Wiley in Immunology & Cell Biology
- Vol. 79 (3) , 274-284
- https://doi.org/10.1046/j.1440-1711.2001.01010.x
Abstract
The interactions of cell surface receptors with their ligands, crucial for initiating many immunological responses, are often stabilized by receptor dimerization/oligomerization, and by multimeric interactions between receptors on one cell with their ligands or cognate receptors on the apposing cell. Current techniques for studying receptor–ligand interactions, however, do not always allow receptors to move laterally to enable dimerization/ oligomerization, or to interact multimerically with ligands on cell surfaces. For these reasons detection of low- affinity receptor–ligand interactions has been difficult. Utilizing a novel chelator-lipid, nitrilotriacetic acid di-tetradecylamine (NTA-DTDA), we have developed a convenient liposome system for directly detecting low-affinity receptor–ligand interactions. Our studies using recombinant soluble forms of murine CD40 and B7.1, and murine and human CD4, each possessing a hexhistidine tag, showed that these proteins can be anchored or ‘engrafted’ directly onto fluorescently labelled liposomes via a metal-chelating linkage with NTA-DTDA, permitting them to undergo dimerization/oligomerization and multimeric binding with ligands on cells. Fluorescence- activated cell sorter (FACS) analyses demonstrated that while there is little if any binding of soluble forms of murine CD40 and B7.1, and murine and human CD4 to cells, engrafted liposomes bind specifically to cells expressing the appropriate cognate receptor, often giving a fluorescence 4–6-fold above control cells. Such liposomes could detect directly the low-affinity interaction of murine CD40 and B7.1 with CD154- and CD28-expressing cells, respectively, and the interaction of CD4 with MHC Class II, which has hitherto defied direct detection except through mutational analysis and mAb blocking studies.Keywords
Funding Information
- National Health and Medical Research Council of Australia (971019)
This publication has 33 references indexed in Scilit:
- Dimeric association and segmental variability in the structure of human CD4Nature, 1997
- CD80, CD86 and CD40 Provide Accessory Signals in a Multiple‐Step T‐Cell Activation ModelImmunological Reviews, 1996
- Covalent Dimerization of CD28/CTLA-4 and Oligomerization of CD80/CD86 Regulate T Cell Costimulatory InteractionsJournal of Biological Chemistry, 1996
- Molecular recognition of antigen involves lattice formation between CD4, MHC class II and TCR moleculesImmunology Today, 1995
- How B and T cells talk to each otherNature, 1994
- Evidence for cell surface association of CD2 and LFA-1 (CD11a/CD18) on T lymphocytesEuropean Journal of Immunology, 1994
- Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1Nature, 1993
- Constitutive expression of high levels of soluble mouse CD4 in transgenic mice does not interfere with their immune functionEuropean Journal of Immunology, 1993
- HIV interactions with CD4: a continuum of conformations and consequencesImmunology Today, 1992
- Crystal structure of an HIV-binding recombinant fragment of human CD4Nature, 1990