The Stability of the Ternary Interferon-Receptor Complex Rather than the Affinity to the Individual Subunits Dictates Differential Biological Activities

• Published in: The Journal of biological chemistry Vol. 283; no. 47; pp. 32925 - 32936
• Main Authors: Kalie, Eyal, Jaitin, Diego A., Podoplelova, Yulia, Piehler, Jacob, Schreiber, Gideon
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 21.11.2008; American Society for Biochemistry and Molecular Biology
• Subjects: Antiviral Agents - chemistry; Flow Cytometry; Gene Expression Profiling; Gene Expression Regulation; Humans; Inhibitory Concentration 50; Kinetics; Models, Molecular; Molecular Conformation; Mutagenesis; Protein Binding; Protein Structure, Tertiary; Receptor, Interferon alpha-beta - metabolism; Receptors, Interferon - chemistry
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M806019200

Type I interferons (IFNs) signal for their diverse biological effects by binding a common receptor on target cells, composed of the two transmembrane IFNAR1 and IFNAR2 proteins. We have previously differentially enhanced the antiproliferative activity of IFN by increasing the weak binding affinity of IFN to IFNAR1. In this study, we further explored the affinity interdependencies between the two receptor subunits and the role of IFNAR1 in differential IFN activity. For this purpose, we generated a panel of mutations targeting the IFNAR2 binding site on the background of the IFNα2 YNS mutant, which increases the affinity to IFNAR1 by 60-fold, resulting in IFNAR2-to-IFNAR1 binding affinity ratios ranging from 1000:1 to 1:1000. Both the antiproliferative and antiviral potencies of the interferon mutants clearly correlated to the in situ binding IC50 values, independently of the relative contributions of the individual receptors, thus relating to the integral lifetime of the complex. However, the antiproliferative potency correlated throughout the entire range of affinities, as well as with prolonged IFNAR1 receptor down-regulation, whereas the antiviral potency reached a maximum at binding affinities equivalent to that of wild-type IFNα2. Our data suggest that (i) the specific activity of interferon is related to the ternary complex binding affinity and not to affinity toward individual receptor components and (ii) although the antiviral pathway is strongly dependent on pSTAT1 activity, the cytostatic effect requires additional mechanisms that may involve IFNAR1 down-regulation. This differential interferon response is ultimately mediated through distinct gene expression profiling.