Notice: Wiley Online Library will be unavailable on Saturday 27th February from 09:00-14:00 GMT / 04:00-09:00 EST / 17:00-22:00 SGT for essential maintenance. Apologies for the inconvenience.
Conflict of interest: A patent has been filed on the reagents and methods described in this proposal
Ashlesha Deshpande and Balananda-Dhurjati Kumar Putcha contributed equally to this work
A method for analyzing ligand–receptor binding kinetics is described, which is based on an engineered FC domain (FChk) that forms a covalent heterodimer. To validate the system, the type I IFN receptors (IFNAR1 and IFNAR2) were expressed as IFNAR1-FChk, IFNAR2-FCkh, and IFNAR1/IFNAR2-FChk fusion proteins. Surface plasmon resonance (SPR) analysis of binary IFNα2a/IFNAR interactions confirmed prior affinity measurements, while the affinity of the IFNα2a/IFNAR1/IFNAR2-FChk interaction reproduced the affinity of IFNα2a binding to living cells. In cellular assays, IFNAR1/IFNAR2-FChk potently neutralized IFNα2a bioactivity with an inhibitory concentration equivalent to the KD measured by SPR. These studies suggest that FChk provides a simple reagent to evaluate the binding kinetics of multiple ligand–receptor signaling systems that control cell growth, development, and immunity.
If you can't find a tool you're looking for, please click the link at the top of the page to "Go to old article view". Alternatively, view our Knowledge Base articles for additional help. Your feedback is important to us, so please let us know if you have comments or ideas for improvement.
Cytokines transmit signals across the cell membrane by oligomerizing cell surface receptors.[1-4] Crystal structure analysis has shown that the basic signaling unit is often a ternary complex, where the cytokine assembles either two identical receptors (homodimerization), or two different receptors (heterodimerization), to activate cellular activity.[1, 5-8] In either case, one receptor chain usually exhibits enhanced affinity to capture ligand to the cell surface, whereas the second chain recognizes this binary complex to form the functional ternary signaling complex. The tuning of receptor–ligand affinities is important not only for regulating the strength of signal through the membrane but also to control targeting of cytokines to specific cells. The direct link between receptor binding and biological function emphasizes the need to accurately measure these protein–protein interactions to improve our understanding of cell communication and facilitate the development of improved cytokine biologics.
The analysis of monomeric ligand–receptor binding kinetics is routinely performed using surface plasmon resonance (SPR). However, cytokine binding to receptor heterodimers, the actual functional units required for signaling, is usually not evaluated. A major reason for this is the three-dimensional nature of biacore chip dextran layers, which do not mimic the planar lipid environment of the cell membrane. To overcome this problem, coiled-coil domains have been used to assemble receptor heterodimers.[9, 10] This eliminates the problem of chip surface heterogeneity by placing the receptors adjacent to one another. However, purification and coupling of the molecules to the chip surface are often problematic. Elegant studies have recently been performed on supported lipid bilayers by attaching histidine-tagged receptors to bis-NTA-coupled lipids that allow the receptors to undergo lateral movement.[11, 12] However, these studies require considerable expertise to perform and do not seem appropriate for general laboratory use.
Immunoglobulin FC domains are often used in biotechnology and therapeutic applications. Several cell surface receptors (e.g., CLTA-4, IL-1R, LFA-3, and TNFR) fused to FC domains have been approved as human therapeutics. Ridgway et al. have extended the utility of the FC by identifying steric “knobs into holes” (kh) mutations in the CH3–CH3 dimer interface that promote formation of an FC heterodimer (FCkh) that allows the production of bispecific Abs. However, the cysteines in the Ab hinge region of the Abs form disulfide bonds regardless of whether FC dimers (e.g., two FCk or two FCh chains), or heterodimers (e.g., an FCk and FCh chain), are assembled.
To generate an improved reagent for the analysis of cytokine-receptor monomer and heterodimer interactions by SPR, the “symmetric” Ab hinge region of FCkh has been replaced with cysteine residues engineered to form a disulfide bond specific for FCkh heterodimer formation. This design has resulted in an improved FCkh reagent that functions as a purification tag, coupling reagent, and heterodimerization domain that allows analysis of monomeric and heterodimeric ligand–receptor interactions. To test the system, the type I IFN receptors, IFNAR1 and IFNAR2, were produced as IFNAR-FChk fusion proteins for SPR analysis (Fig. 1). Type I interferons (IFNs) induce antiviral, antiproliferative, and immunomodulatory activities on diverse cell types.[15-17] Several studies have shown that receptor binding affinity is directly related to the biological activity of the IFNs.[18-20] In addition, biophysical studies have characterized IFN/IFNAR receptor interactions using diverse methods.[21, 22] For these reasons, the type I IFN receptor system was used to test the functionality of FChk to assemble, purify, and characterize IFN binding kinetics to monomeric and heterodimeric IFNARs. SPR analysis demonstrated that the affinity of the IFNα2a/IFNAR1/IFNAR2-FChk interaction was equivalent to the affinity of IFNα2a binding to living cells. These studies confirm the usefulness of this simple system for studying a wide variety of diverse protein–protein interactions with affinities that span over five orders of magnitude.
Design and production of a disulfide-linked FCkh heterodimer
A FC heterodimer (FCkh) was designed based on a previously described “knob-into-holes” strategy by inserting knob (k, T366Y) and hole (h, Y407T) mutations into separate plasmids (FCh and FCk) encoding an antibody IgG2a heavy-chain FC region. Using the IgG2a crystal structure (PDB ID = 1IGT), cysteine residues were positioned into FCk and FCh to selectively form an interchain disulfide bond upon FCkh heterodimer formation. To accomplish this, the FC dimer interface was interrogated for inter-interface amino acid positions (within ∼8 Å of one another) that would allow disulfide bond formation upon heterodimer formation, but not upon FC homodimerization. Based on this analysis, an E376C mutation was added to the FCk chain and a “GGCGT” sequence was encoded at the C-terminus of FCh, following residue F472.
Coexpression of FCk and FCh chains efficiently formed (∼100%) disulfide-linked FCkh heterodimers rather than FCkk and FChh homodimers (Fig. 2). FCk expressed alone does not assemble into disulfide-linked FCkk dimers, whereas expression of FCh efficiently forms disulfide-linked FChh homodimers. The solution structure of FCkh was determined by small-angle X-ray scattering (SAXS) to confirm that FChk adopts the same overall structure as the FC crystal structure (1IGT). Radius of gyration (Rg) and dmax values obtained from the SAXS data (Rg = 28.8 Å, dmax = 75 Å) were similar to values calculated for the FC crystal structure (Rg = 25.5 Å, dmax = 82.5). The fit of the FC crystal structure into the average bead model suggests that the N-termini of the CH2 domains in FCkh are separated by ∼21 Å [Fig. 2(C)]. This distance is approximately twice as large as observed for the N-termini of heterodimeric coiled-coil assembly domains.[24, 25]
Production and ligand-binding properties of IFNAR1-FChk and IFNAR2-FCkh monomers
To determine if FCkh could be used to purify and attach receptors to biacore chips for SPR experiments, the extracellular regions of IFNAR1 and IFNAR2 were cloned in frame with FCh and FCk, respectively. To assemble IFNAR1-FChk and IFNAR2-FCkh fusion proteins (Fig. 1), plasmids encoding IFNAR1-FCh and FCk, as well as IFNAR2-FCk and FCh, were coexpressed in insect cells. IFNAR1-FChk and IFNAR2-FCkh were purified from the expression media by protein A and size exclusion chromatography [SEC, Fig. 3(A)]. On the size exclusion column, IFNAR1-FChk and IFNAR2-FChk ran at molecular weights (MWs) of 122 and 82 kDa, respectively [Fig. 3(A)]. FChk disulfide bond formation was confirmed by SDS-PAGE analysis of IFNAR1-FChk and IFNAR2-FCkh under oxidizing and reducing conditions [Fig. 3(B)]. Under oxidizing conditions the fusion proteins ran as single bands with MWs observed by SEC. However, on reducing gels, the proteins separated into two bands corresponding to IFNAR1-FCh and FCk, or IFNAR2-FCk and FCh [Fig. 3(B)]. This analysis confirmed that FCkh can be used to assemble monomeric IFNAR1-FCkh and IFNAR2-FCkh fusion proteins as opposed to commonly produced FC receptor dimers.
The IFNα2a/IFNAR2 interaction was studied by injecting IFNα2a over IFNAR2-FCkh, which was coupled to a biacore chip using an anti-FC antibody [Fig. 4(A)]. Sensorgrams from three experiments were fit to a 1:1 binding model resulting in ka and kd values of 5.5 × 106 M−1s−1 and 0.032 s−1, which corresponds to an equilibrium dissociation constant (KD) of 5.8 nM (Table 1). The observed binding constants are consistent with previous values obtained for the IFNα2a/IFNAR2 interaction using different experimental methods. IFNα2a was also injected (78–5000 nM) over IFNAR1-FChk coupled to biacore chip surfaces [Fig. 4(B)]. Three equilibrium experiments yielded a KD of 3080 nM for the IFNα2a/IFNAR1-FChk interaction. A KD value of 3692 nM was obtained from rate constants (ka = 6.5 × 105 M−1s−1 and kd = 2.4 s−1), determined from a single kinetic experiment. The KD value obtained for the IFNα2a/IFNAR1-FChk interaction is also similar to previously reported values (KD = 3–5 μM). Together, these studies validate the use of the FCkh heterodimers for SPR analysis of cytokine–receptor interactions.
Table 1. Binding Parameters for IFNα2a/IFNAR-FChk Interactions
k1a × 105 (M−1 s−1)
k2a × 105 (M−1 s−1)
k2d × 10−4 (s−1)
Each sensorgram was fit with a heterogeneous ligand model.
Sensorgrams fit with 1:1 model.
Sensorgrams fit with heterogeneous ligand model.
Molar ratio of IFNAR1-FChk to IFNAR2-FCkh, where IFNAR2-FCkh was coupled at constant level of 40 RU.
Production and analysis of IFNAR1/IFNAR2-FChk heterodimers
To evaluate IFNα2a binding to IFNAR1 and IFNAR2, plasmids encoding IFNAR1-FCh and IFNAR2-FCk were coexpressed in insect cells to produce an IFNAR1/IFNAR2-FChk heterodimer (Fig. 1). Media from the expression experiment were purified by protein A chromatography and SEC [Fig. 3(A)]. The estimated MW of IFNAR1/IFNAR2-FChk on SEC is 160,300, which is consistent with its predicted MW of 137,405. The predicted MW includes 15,585 Da of N-linked carbohydrate, which corresponds to insect cell-derived hexasaccharides (1039 Da each) attached to each of the 15 predicted NXS/T-linked sites in the heterodimer. SDS-PAGE analysis of IFNAR1/IFNAR2-FChk under oxidizing and reducing conditions confirmed that IFNAR1-FCh and IFNAR2-FCk chains are covalently linked by a disulfide bond [Fig. 3(B)]. Thus, the same MW and 1:1 stoichiometry of IFNAR1/IFNAR2-FChk, as well as IFNAR1-FChk and IFNAR2-FCkh, was confirmed by SEC and SDS-PAGE analysis.
SPR sensorgrams collected for IFNα2a binding to the IFNAR1/IFNAR2-FChk were complex, meaning that they could not be fit with a simple 1:1 binding model [Fig. 4(C)]. As IFNAR1/IFNAR2-FChk is an assembly of two receptors (IFNAR1 and IFNAR2), a heterogeneous ligand model (HLM) incorporating two distinct rate equations was used to fit the sensorgrams. IFNα2a/IFNAR1/IFNAR2-FChk sensorgrams fit with the HLM resulted in one binding constant equivalent to the IFNα2a/IFNAR2-FCkh binary complex (KD = 7.2 nM), whereas the second KD value (26 pM) approximated the KD of IFNα2a binding to living cells and to IFNARs attached to supported lipid bilayers (Table 1[18, 22]. The HLM yielded the best agreement to the experimental sensorgrams, which is shown by comparing 1:1, HLM, and two-state model fits in Figure 4(C). The KD derived from each model ranges from 120 pM (1:1 model, Table 1) to 8 pM for the two-state model (Table 2). The HLM and two-state models were also applied to the IFNα2a/IFNAR2-FCkh sensorgrams as a control [Fig. 4(B), Tables 1 and 2]. These studies demonstrated that the HLM yielded essentially the same KD and rate constants as observed for the 1:1 model [Fig. 4(B) and Table 2]. The two-state model applied to the IFNα2a/IFNAR2-FCkh sensorgrams yielded the same KD value (Table 2) obtained using the 1:1 and HLM, with an additional set of rate constants that were not required for the fitting. Interestingly, the second off-rates (k2d) in the two-state model were decreased by ∼10-fold relative to off-rates obtained in the 1:1 and HLM. Overall, this suggests that the appropriate model for analysis of the IFNα2a/IFNAR1/IFNAR2-FChk sensorgrams is the HLM.
Table 2. Two-State Binding Parameters for IFNα2a/IFNAR-FChk Interactions
Use of the HLM suggests that IFNα2a forms a mixture of IFNα2a/IFNAR2 binary complexes and IFNα2a/IFNAR1/IFNAR2 ternary complexes on the chip surface. The chemical purity of IFNAR1/2-FChk (Fig. 3) suggests that the heterogeneous binding properties are not due to problems with the stoichiometry of the heterodimer. It is possible that a fraction of IFNAR1-FCh within the IFNAR1/IFNAR2-FChk heterodimer is unable to bind IFNα2a, owing to steric occlusion, upon attachment to the SPR chip surface, which prevents capture of IFNAR2/IFNα2a complexes by IFNAR1. The percent of IFNα2a/IFNAR1/IFNAR2-FChk ternary complexes formed, relative to IFNα2a/IFNAR2 binary complexes, was estimated to be 55% from analysis of RUmax values calculated in the HLM fitting routine. Good agreement was observed between the calculated RUmax values, derived from the HLM, and the RUmax value observed in the SPR sensorgrams. Specifically, the sum of the two calculated RUmax values was 5.3 and 6.5 RU (11.8 total), respectively, whereas the observed RUmax from the 25 nM IFNα2a sensorgram was 10.4 RU. To further validate the affinity of the IFNα2a/IFNAR1/IFNAR2-FChk interaction determined by SPR, the ability of IFNAR1/IFNAR2-FChk to neutralize IFNα2a-mediated gene induction was tested using cells stably transfected with a luciferase reporter under control of the IFN-inducible 6-16 gene promoter (Fig. 5). The inhibitory concentrations (IC50) of IFNAR1/IFNAR2-FChk required to block the activity of 8 pM or 5 nM IFNα2a were 25.5 pM and 11.6 nM, respectively. From these experiments, the IFNAR1/IFNAR2-FChk affinity constant (Ki) was estimated as 12.5–18.5 pM using the Cheng-Prusoff equation, which is similar to the KD value determined by SPR (Table 1).
IFNAR1/IFNAR2-FChk was coupled at low levels to prevent mass transport, suggesting that the resulting KD represents the inherent stability of the IFNα2a/IFNAR1/IFNAR2 ternary complex. The binding results obtained with IFNAR1/IFNAR2-FChk were compared against biacore chips coupled with monomeric IFNAR1-FChk and IFNAR2-FCkh in a similar manner to the studies first performed by Lamken et al. on supported lipid bilayers. For these experiments, a constant level of IFNAR2-FCkh was captured (40 RU) on the chip with three different amounts of IFNAR1-FChk corresponding to IFNAR1/IFNAR2 molar ratios of 4.4:1, 1.6:1, and 1:0.5, respectively (Table 1). For each surface, a sensorgram corresponding to a single injection of 10 nM IFNα2a was fit with the HLM [Fig. 5(B)]. As previously observed with IFNAR1/IFNAR2-FChk, one set of binding constants corresponded to the IFNα2a/IFNAR2 interaction. However, the KD values for the second interaction ranged from 1.7 to 40 nM. The on-rate for the second interaction was ∼1 × 105 M−1 s−1, which is similar to the on-rate observed for the IFNα2a/IFNAR1-FChk interaction (Table 1). The off-rate of the second binding site was intermediate between the IFNα2/IFNAR1/IFNAR2-FChk and IFNα2/IFNAR2-FCkh interactions (∼0.002–0.005 s−1). The levels of IFNAR1-FChk and IFNAR2-FCkh coupled did not differ significantly from IFNAR1/IFNAR2-FChk (∼100 RU). This suggests that the heterogeneous positioning of IFNAR1-FChk and IFNAR2-FCkh prevents efficient assembly of the IFNα2a/IFNAR1/IFNAR2 complex. However, the IFNα2a off-rate on the mixed surfaces is slower than for IFNAR2 alone, which may be caused by IFNα2a being shuttled between IFNAR1-FChk and IFNAR2-FCkh that are separated in space by distances greater than IFNAR1 and IFNAR2 attached to a single FChk domain.
In this study, structure-based engineering was used to produce a disulfide-linked FChk domain to allow the characterization of cytokine binding to individual receptor chains and to signaling competent receptor heterodimers. As an example system, monomeric IFNAR1-FChk and IFNAR2-FCkh receptors, as well as IFNAR1/IFNAR2-FChk heterodimers were produced for binding studies. Because of the large body of biochemical and biological data, and the distinct MWs of the extracellular receptor chains (IFNAR1 ∼50,000 and IFNAR2 ∼25,000), the IFNAR receptor system was ideal to characterize the utility of FChk. SPR analysis of IFNα2a binding to IFNAR1/IFNAR2-FChk yielded a KD of 26 pM, which is very similar to the affinity of IFNα2a binding to cells (KD ∼ 26 pM) and to IFNARs attached to supported lipid membranes.[18, 22] This suggests that the IFNAR1/IFNAR2-FChk heterodimers can mimic some features of the membrane-bound receptor chains.
The high-affinity IFNα2a/IFNAR1/IFNAR2-FChk interaction could not be reproduced by coupling monomeric IFNAR2-FCkh and IFNAR1-FChk to the SPR chip. This likely reflects the heterogeneity of the dextran/anti-FC antibody surface used to attach the proteins to the chip surface. Often, heterogeneity describes amine coupling-induced heterogeneity in the protein coupled to the matrix, which when extreme, can prevent accurate data collection and binding constants. However, in this case, we are describing positional heterogeneity of the FC-coupled IFNAR-FCs in the dextran matrix. Specifically, all IFNAR1-FChk and IFNAR2-FCkh are coupled homogeneously on the chip surface through the FChk domain. However, within the anti-FC/dextran matrix, IFNAR1-FChk and IFNAR2-FCkh are randomly oriented in the three-dimensional space, which prevents IFNAR1 and IFNAR2 from simultaneously binding to IFNα2a. This technical issue is overcome by the IFNAR1/IFNAR2-FChk heterodimer, which allows efficient ternary complex formation. Interestingly, these heterogeneous surfaces generate off-rates equivalent to what was observed at low IFNAR1/IFNAR2 levels on supported lipid membranes. These data reinforce the importance of characterizing individual cytokine–receptor interactions, as well as cytokine engagement by receptor heterodimers that more accurately reflect binding at the cell surface.
In addition to a robust reagent for characterizing protein–protein interactions, IFNAR1/IFNAR2-FChk potently antagonized IFNα2a biological activity with an IC50 value matching the KD determined by SPR. Thus, the FChk domain may be a valuable scaffold for producing potent cytokine antagonists, which could have medical relevance. For example, type I IFNs have been implicated in the initiation, progression, and pathology of systemic lupus erythematosus (SLE).[29, 30] Blocking type I IFN biological activity is currently being tested as a therapy for SLE and might also be important in other autoimmune diseases such as diabetes.[31-33]
Biochemical and SAXS studies confirm that FChk forms a disulfide-linked FC heterodimer that mimics the FC homodimer crystal structure. Thus, FChk forms a stable scaffold to position receptors ∼20 Å apart, or further with increased linker lengths, for solution and solid-phase binding studies. Overall, our studies demonstrate that IFNAR-FChk fusion proteins are easily purified and suitable for capture on biacore chips for binding studies. These features of the system provide an opportunity for high-throughput analysis of quantitative cytokine–receptor kinetics using a standardized analysis platform. Currently, greater than 50 molecules, designated as IFNs and interleukins, are amenable to study using this strategy.[1, 34, 35] Preliminary studies have confirmed that FChk provides an excellent scaffold for characterizing ErbB growth factor receptor interactions (K. Putcha and M.R. Walter, personal communication) and other systems are currently being evaluated.
Materials and Methods
IFNα2 expression and purification
A plasmid containing IFNα2a (pPAL7-IFNα2a) was obtained from Philip Bryan, which encodes a subtilisin prodomain IFNα2a fusion protein. Protein expression was performed by the autoinduction method. Briefly, cells containing pPAL7-IFNα2a were grown at 37°C overnight with shaking (300 rpm) in ZYP 0.8G media containing 100 μg mL−1 carbenicillin. The overnight culture was diluted 1:20 into ZYP-5052 media and grown for 4 h at 37°C, followed by a 20-h incubation at 15°C with shaking (300 rpm). The cells were collected by centrifugation, followed by sonication in a buffer containing 100 mM Tris-acetate, pH 8.0 and 1.0 mM EDTA. The lysate was clarified by centrifugation (48,000g) and loaded onto eXact media (BIO-RAD). The protein was eluted with 10 mM sodium azide in 100 mM sodium acetate, pH 7.4 and subsequently purified by ion exchange and SEC. IFNα2a purified by this method retained two additional amino acids (Thr-Ser) at its N-terminus.
FChk and receptor-FChk fusion cloning, expression, and purification
DNA encoding the murine IgG2a FC region, residues 251-472 (PDB ID 1IGT), was cloned into the insect expression vector pMT (Invitrogen) by PCR. Amino acid changes E376C and T389Y were encoded into one FC sequence to generate a modified FC knob (FCk) plasmid, pMTA-FCk. In a second wild-type FC, a Y438T mutation was inserted and amino acids “GGCGT” were encoded at the C-terminus, following residue F472 to yield plasmid pMTA-FCh. The extracellular regions of IFNAR1 (residues 28-436, uniprot ID P17181) and IFNAR2 (residues 31-243, uniprot ID P48551) were inserted in frame into pMTA-FCh and pMTA-FCk, respectively, using SacII and BamHI restriction sites, resulting in plasmids pMTA-IFNAR1-FCh and pMTA-IFNAR2-FCk.
Expression plasmids were transfected into Drosophila S2 cells using the manufacturer's protocols (Invitrogen). Stable cell lines were selected with hygromycin and protein expression was induced by addition of 0.5 mM Cu2SO4 at a cell density of 5 × 106 cells per milliliter in serum-free media (Lonza) containing 20 mMl-glutamine. Expressed media were harvested after 7 days, clarified by centrifugation, and filtered through a 0.2-μm PES filter. Receptor-FChk fusion proteins were purified using a 1 mL Protein A affinity column (Thermo scientific) equilibrated in 20 mM Tris-HCl, pH 8.0 and 150 mM NaCl. Bound protein was washed with 50 column volumes of equilibration buffer and eluted in 2M arginine, pH 3.8. The pH of the column fractions was adjusted by addition of 1M Tris-HCl, pH 8.0, followed by dialysis against 20 mM Tris-HCl, pH 8.0 and 150 mM NaCl. Pooled fractions were concentrated and injected on a Superdex 200 (GE Healthcare) size exclusion column in running buffer of 20 mM HEPES, pH 7.9 and 150 mM NaCl.
SPR data collection and analysis
SPR data collection and analysis were performed using a Biacore T-200 (GE healthcare). Monomeric and heterodimeric IFNAR-FChks were coupled to CM5 biacore chips using an anti-FC Ab coupling kit according to the manufacturer's instructions (GE healthcare). IFNα2a was injected over the surfaces at 100 μL min−1 in a running buffer of 10 mM HEPES, 150 mM NaCl, 0.015% P20 (GE Healthcare), and 150 μg mL−1 bovine serum albumin (Sigma). IFNα2a contact times for each experiment were 75 s. The dissociation times were 75, 240, and 400 s for IFNAR1-FChk, IFNAR2-FCkh, and IFNAR1/IFNAR2-FChk, respectively. Fresh IFNAR-FChk surfaces were prepared for each cycle by a 3-min injection of 10 mM glycine, pH 1.7, followed by an injection of new IFNAR-FC fusion protein. Sensorgrams were fit to appropriate 1:1 and HLMs using the predefined templates in the Biacore T-200 evaluation software version 1.0.
X-ray scattering data on FChk (8.8 mg mL−1) were collected on the SIBYLS beamline at the Advanced Light Source, Berkley. Scattering curves were processed with the program PRIMUS within the ATSAS package. Bead models were derived from the scattering curve with the program DAMIN. A total of 10 models were calculated and a final averaged bead model was calculated with DAMAVER.
Luciferase activity assay
HT1080 cells, containing a luciferase reporter downstream of the IFN inducible 6-16 promoter (HL116 cells), were used to monitor IFNAR1/IFNAR2-FChk neutralization of IFNα2a. HL116 cells (4 × 104 cells) were plated in white opaque 96-well plates and incubated overnight at 37°C. A constant concentration of IFNα2a (8 pM or 5 nM) was incubated with serially diluted IFNAR1/IFNAR2-FChk heterodimers in media (DMEM-glutamax) for 30 min at 37°C before addition to HL116 cells. The plates were incubated for 5 h at 37°C. Following the 5-h incubation, the plates were moved to room temperature for 10 min, followed by the addition of 50 µL of luciferase assay reagent (Steady-Glo, Promega) to each well. Luminescence was measured on a Biotek Synergy 2 plate reader and analyzed with PRISM software using a four-parameter fit with variable slope (Graphpad Inc).
The authors thank Philip Bryan and Natasha Oganesyan for providing the pPal7-IFNα2a vector and expertise in protein purification, Dario Vignali for the murine IgG2a plasmid, and Gilles Uzé for HL116 cells. The SIBYLS beamline at the Advanced Light Source, Lawrence Berkeley National Laboratory, is supported in part by the DOE Program Integrated Diffraction Analysis Technologies (IDAT) under Contract Number DE-AC02-05CH11231 with the U.S. Department of Energy. Access to the Biacore T-200 is made possible by the University of Alabama at Birmingham Multidisciplinary Molecular Interaction Core.