- Transcreener® ADP2 Assay kit is a far-red competitive FP immunoassay based on the detection of ADP
- Transcreener® can monitor any enzymatic reaction that produces ADP (ATP range is 0.1 - 1000 µM)
- PHERAstar®FS, CLARIOstar® and POLARstar® Omega validated by BellBrook Labs
Table of contents
BellBrook Labs offers a variety of high throughput screenings assays for enzymes. The Transcreener® ADP2 FP assay can be used to detect the activity of any kinase or ATPase. This simple ADP detecting method is universal for all ADP-producing enzymes and can be used with any substrate.
In this application note we show ADP/ATP standard curves created during performing the Transcreener® assay using different microplate readers from BMG LABTECH.
The Transcreener® ADP2 Assay is a ﬂuorescence polarization immunoassay based on the detection of ADP by an antibody (Figure 1). This assay platform provides the possibility to universally interrogate all enzymes that catalyze group transfer reactions with ATP. In step one of the assay, enzymes catalyze the transfer of phosphate from ATP to a protein, peptide, lipid or small molecule resulting in the accumulation of ADP.
In step two the Transcreener® ADP2 Detection Mixture, which contains an ADP Alexa633 tracer bound to an anti-ADP antibody, is added. If there is enzymatic activity resulting in necessary ADP then the bound tracer is displaced by the ADP. The free tracer rotates quickly leading to a lower polarization value. If there is no free ADP because of no enzymatic activity, the tracer is still bound to the antibody. This whole construct rotates very slowly giving a higher polarization number. Therefore, ADP production leads to a decrease in ﬂuorescence polarization.
Materials & Methods
- Black 384 well and 1536 well microplates from Corning
- Black 96 well half area ﬂat bottom polystyrene NBS™ microplate, Corning
- Transcreener® ADP2 Assay from BellBrook Labs, Madison, WI, (including ADP Alexa633 Tracer, ADP2 Antibody, Stop & Detect Buffer B, ATP, and ADP)
Transcreener® HTS assay performance were identiﬁed by running a 10 µM ATP/ADP and 0.1 µM ATP/ADP standard curve (24 replicates), as standard curves of this type mimic enzyme reactions. Starting with 10 µM or 100 nM ATP, ADP was added in increasing amounts and ATP is decreased proportionately, maintaining a total adenine nucleotide concentration of 10 µM and 100 nM respectively.
ADP Detection Mixture
This solution contains 4 nM tracer, 1x stop and detect buffer, and 15 µg/ml (for 10 µM) and 1 µg/ml (for 100 nM). The ADP detection mixture is diluted two fold in the well which leads to the following ﬁnal concentrations in the well: 2 nM tracer, 0.5x buffer and antibody.
The ﬁnal antibody concentration per well was 0.5 µg/ml (100 nM standard curve) and 7.5 µg/ml (10 µM standard curve). Please note that the optimal antibody concentration can differ signiﬁcantly depending on the enzymatic reaction conditions. For optimal assay performance it is necessary to do an antibody titration under the speciﬁc enzyme and buffer conditions used in your experiment.
10 µl of standard and 10 µl of detection mixture were mixed in a 384-well microplate which was sealed and incubated at room temperature for 1 hour. After incubation the sealer was removed and the plate was measured. For the 96-well half area plate the ﬁnal volume in the well was 140 µl. For the 1536-well plate the ﬁnal volume in the well was 8 µl.
|FLUOstar / POLARstar Omega||CLARIOstar||PHERAstar FS|
|Detection Mode||Fluorescence Polarization|
|Method||Endpoint, Top optic|
|Well Format||96-well||96 well, 384-well, 1536-well||96 well, 384-well, 1536-well|
|Optic settings||Ex-Filter: 630-10, Em-Filter: 670-10||Ex-Filter: 590-50, Em-Filter: 675-50||Transcreener specific FP optic module: FP 590 675 675|
|mP target value||Was set to be 20 mP for a well containing the free tracer|
Results & Discussion
Figure 2 shows the ADP/ATP standard curve measured in the 96 well format. Graphing on the log scale eliminates the point that corresponds to zero. To include all twelve points along the curve, the value for 0 µM ADP/10 µM ATP was graphed at 0.01 µM position.
Figure 3 and 4 show the standard curves measured in 384 well and 1536 well format, respectively.
The universally generic nature of the Transcreener® ADP2 kit will reduce assay development efforts thus allowing HTS to occur earlier. As a characteristic parameter for the quality of the assay, a Z′ value > 0.7 was calculated, which represents an excellent assay performance. Z′ values between 0.5 and 1 indicate a highly robust screening assay and reﬂect high quality of instrumentation.
Based on the data exemplarily shown in this application note, the POLARstar Omega, the CLARIOstar as well as the PHERAstar FS were certiﬁed for the Transcreener® ADP2 FP assay.
Transcreener® is a patented technology of BellBrook Labs.