365Excellent assay performance of THUNDER™ TR-FRET cell-based cytokine assays performed on the PHERAstar FSX

Introduction

Cytokines are important regulators of cell proliferation, differentiation, and immune response¹. Since their roles are not completely understood yet, both basic and drug discovery research require accurate cytokine quantification methods. THUNDER™ Biomarker Assays are designed to enable the simple, rapid, sensitive, and robust quantification of biomarkers in cell supernatants. BioAuxilium’s enhanced Time-Resolved Förster Resonance Energy Transfer (TR-FRET) technology² is well-suited for cytokine quantification, with distinct advantages over conventional ELISA: homogeneous format, low sample volume, one-step protocol, wider dynamic range, high-throughput capability, and proven robustness and reproducibility.

Here we describe the validation of the PHERAstar FSX multi-mode microplate reader for measuring a panel of five THUNDER™ human cytokine assays.

Assay Principle

THUNDER™ cytokine assays are homogeneous sandwich immunoassays (Figure 1). One antibody is labeled with a long lifetime Europium chelate donor (Eu-Ab1) and the second with a far-red acceptor fluorophore (FR-Ab2). Upon excitation of the Europium chelate at 320 or 340 nm, energy is transferred from the donor to the acceptor fluorophore if they are sufficiently close for FRET. The emission by the acceptor of a long-lived TR-FRET signal at 665 nm is measured after a time delay.

Materials & Methods

• 384-well, white low-volume plates (PerkinElmer^®)
• KIT-IFNGP-100, KIT-IL1B-100, KIT-IL12-100, KITCCL2 100, and KIT-TNFA-100 assay kits (Bioauxilium Research)
• Human recombinant proteins (R&D Systems^®)
• PHERAstar^® FSX microplate reader (BMG LABTECH)

Experimental Procedure
Protocols were conducted as per BioAuxilium’s recommendations³. The standard curves were run using each kit’s Assay Buffer. Standards (15 µL) were added to 384-well white assay plates followed by the addition of the Antibody Mix (5 µL) for detection of the target cytokine. The plates were incubated at room temperature for the appropriate time and read on the PHERAstar FSX using the settings recommended for THUNDER™. For comparison, plates were also read on a competing HTS microplate reader equipped for TRF laser excitation. Data were expressed as (665/620) * 1,000 and are the mean ± SD of three wells per point. Data were fit to a 4PL model with 1/Y2 data weighting (GraphPad). As per BioAuxilium’s protocol, the limit of detection (LOD) and lowest limit of quantification (LLOQ) were calculated by adding 2 or 10 standard deviations (SD), respectively, to the mean background counts (zero standard; 12 replicate wells).

Instrument Settings

Results & Discussion

Figure 2 shows a typical non-linear standard curve for human IL-1β. The assay read on the PHERAstar FSX showed an excellent well-to-well precision, with the mean percentage coefficient of variation (CV%) for the calibration point signals at 1.7% (3.8% for the competing HTS plate reader). The LOD and LOQ values were approximately 25-fold lower compared to those obtained with the competitor, regardless of the instrument settings used, thereby significantly extending the assay dynamic range. Furthermore, the signal-to-background (S/B) ratio at the highest standard was also higher with the PHERAstar FSX.

The higher assay sensitivity of the PHERAstar FSX is evident in Figure 3, which shows a linear plot of the low-concentration part of the human IL-1β standard curve. For the PHERAstar FSX, there is a clear systematic signal increase over the 0-30 pg/mL range. This, combined with the very low CVs (1.9% versus 3.4% for the competing HTS plate reader), makes it possible to discriminate between these very low concentrations. 

The analytical (LOD) and functional (LLOQ) sensitivities obtained with the evaluated human cytokine assays are summarized in Table 1. In all cases, the PHERAstar FSX exhibited a higher assay sensitivity compared to the competitor and our internal data³, decreasing the LOD to single digit pg/mL. These data demonstrate that the PHERAstar FSX is particularly advantageous for performing quantitative THUNDER™ cytokine assays.

Table 1: Performance of THUNDER™ cytokine assays on the PHERAstar FSX and the competing HTS reader.

Of note, systematic variations to the instrument settings (i.e., gain, delay, and integration time) used for reading the assays had no significant impact on the overall performance (LOD, LLOQ, S/B; data not shown), demonstrating the robustness of THUNDER™ cytokine assays. Readings of sample plates on eight different PHERAstar FSX were highly consistent and exhibited minimal variations (e. g., standard deviation of 1.6% for slope of IL-1β standard curves).

Conclusion