Ligand binding kinetics of IL-2 and IL-15 to heteromers formed by extracellular domains of the three IL-2 receptor subunits

• Published in: International immunology Vol. 7; no. 11; p. 1839
• Main Authors: Balasubramanian, S, Chernov-Rogan, T, Davis, A M, Whitehorn, E, Tate, E, Bell, M P, Zurawski, G, Barrett, R W
• Format: Journal Article
• Language: English
• Published: England 01.11.1995
• Subjects: Amino Acid Sequence; Animals; Biopolymers; Epitopes - immunology; Extracellular Space - chemistry; Extracellular Space - immunology; Extracellular Space - metabolism; Humans; Interleukin-15; Interleukin-2 - metabolism; Interleukin-2 - pharmacology; Interleukins - metabolism; Kinetics; Ligands; Mice; Protein Binding - drug effects; Protein Binding - immunology; Receptors, Interleukin-2 - metabolism; Structure-Activity Relationship
• ISSN: 0953-8178; 1460-2377
• DOI: 10.1093/intimm/7.11.1839

Studies on the binding of IL-2 to its receptor (IL-2R) have generally been limited to receptors expressed on cell surfaces. This has hampered detailed kinetic and mechanistic studies at the molecular level. We have prepared the soluble extracellular domains of all three receptor subunits (called alpha, beta and gamma) by recombinant techniques and have used these to perform detailed kinetic studies of their binding properties using the technique of surface plasmon resonance. We describe a novel approach whereby the receptors are assembled on an antibody surface, being held by an epitope engineered into the C-terminus of each of these domains. Thus the receptors are oriented naturally leading to homogeneous ligand binding kinetics. We have characterized the interactions of the heteromeric complexes of these subunits with mouse and human IL-2 and their analogs, as well as the recently discovered cytokine, IL-15. We have also studied the extracellular domains of the mouse receptor subunits for the first time and have used these as well as mouse-human hybrid receptors to probe the mechanism of assembly of these complexes. We show that no additional proteins are required to reproduce the properties of these complexes in vitro. In addition, kinetic studies with site-specific analogs of IL-2 and the mouse-human receptor hybrids clearly indicate that the extracellular domains of alpha and beta can together readily bind ligand with kinetic properties distinct from those of the constituent subunits. In contrast, a complex containing ligand and the extracellular domains of beta and gamma was comparatively difficult to assemble and required prolonged exposure to IL-2. Our method enabled us to calculate the stoichiometry of these complexes and to determine that anchoring these subunits is necessary to efficiently drive complex formation. The kinetic and equilibrium differences between the mouse and human receptor complexes, and between IL-2 and IL-15 binding to these receptors clarify the roles of the alpha and gamma subunits in the differential response of cells to different cytokines that may be present simultaneously in the environment.