Total Aurora B assay principle

The Total-Aurora B assay quantifies the expression level of Aurora B in a cell lysate. Unlike Western Blot, the assay is entirely plate-based and does not require gels, electrophoresis, or transfer. The Total-Aurora B assay uses two labeled antibodies: one coupled to a donor fluorophore, the other to an acceptor. Both antibodies are highly specific for a distinct epitope on the protein. In presence of Aurora B in a cell extract, the addition of these conjugates brings the donor fluorophore into close proximity with the acceptor and thereby generates a FRET signal. Its intensity is directly proportional to the concentration of the protein present in the sample, and provides a means of assessing the protein’s expression under a no-wash assay format.

Total-Aurora B 2-plate assay protocol

The 2 plate protocol involves culturing cells in a 96-well plate before lysis, then transferring lysates into a 384-well low volume detection plate before the addition of Total Aurora B HTRF detection reagents. This protocol enables the cells' viability and confluence to be monitored.

Total-Aurora B 1-plate assay protocol

Detection of total Aurora B with HTRF reagents can be performed in a single plate used for culturing, stimulation, and lysis. No washing steps are required. This HTS designed protocol enables miniaturization while maintaining robust HTRF quality.

Activation of Total and Phospho-Aurora B (Thr232) measured on HeLa cells

HeLa cells (Immortalized Human cervical cancer cell line) were seeded in a 96-well culture-treated plate at 100,000 cells/well for 24 hours in complete culture medium for adhesion. After cell culture medium removal, they were treated with increasing concentrations of Nocodazole for 20h at 37° C, 5% CO2. After overnight treatment (20h), the cell culture medium was removed and 50 µl of supplemented Lysis Buffer#1 (1X) were dispensed into each well for 30 min at RT under gentle shaking. After cell lysis, 16 µL of lysates were transferred into a 384-well low volume white microplate and 4 µL of the HTRF Total Aurora B or Phospho-Aurora B (Thr232) detection antibodies were added. The HTRF signal was recorded after an overnight incubation.
 

Nocodazole is a microtubule destabilizer inducing a G2/M cell cycle arrest. It has been demonstrated that Nocodazole-treated cells show higher Aurora protein expression levels, to overcome cell cycle arrest.
 

As expected, the results obtained show increased levels of Total and Thr232 Phosphorylated Aurora B proteins  upon treatment with Nocodazole.

Specificity and selectivity of HTRF Total Aurora B assay using gene silencing (SiRNA)

HeLa cells were treated with 25 nM of SMARTPool ON-TARGETplus siRNA (Horizon) specifically targeting Aurora A (#L-003545-01-0005), Aurora B (# L-003326-00-0005), and Aurora C (#L-019573-00-0005),  or with a non-targeting siRNA (# D-001810-10-20, included as control), in a 96-well plate (25,000 cells/well) under 100 µL for 24H. After cell culture medium removal, cells were stimulated by adding 300 nM Nocodazole in complete cell culture medium for an additional 24h incubation at 37°C, 5% CO2. After medium removal, cells were lysed with 50 µL lysis buffer #1 (1X) for 30 min at RT under gentle shaking, and 16 µL of lysates were transferred into a low volume white microplate before the addition of 4 µL of premixed HTRF Total Aurora B detection antibodies. The HTRF signal was recorded after an overnight incubation at RT.

Cell treatment with Aurora B siRNA led to a significant downregulation of Aurora B,  with a 58% signal decrease compared to the cells transfected with the non-targeting siRNA.

Despite high homology between the 3 family proteins, no decrease in signal was observed for cells treated with Aurora A or Aurora C siRNA, demonstrating the specificity of the kit.

Validation on various Human cell lines

Immortalized human cell lines HepG2 (Liver Cancer), HeLa (Cervix Cancer), HEK293, and HCT116 (Colon Cancer) were plated in 96-well culture plates at a density of 25,000 or 100,000 cells /well and incubated for 24 hours at 37°C, 5% CO2. After cell culture medium removal, cells were stimulated by adding 300 nM Nocodazole in complete cell culture medium for 20H at 37°C, 5% CO2. Cells were lysed after medium removal with 50 µL of supplemented lysis buffer #1 (1X), for 30 min at RT under gentle shaking.

The Aurora B protein expression level was assessed with the HTRF Total Aurora B kit. Briefly, 16 µL of cell lysate were transferred into a low volume white microplate followed by 4 µL of premixed HTRF detection reagents. The HTRF signal was recorded after an overnight incubation at RT.  Note that cell density optimization is mandatory to be within the dynamic range of the kit.

The HTRF Total Aurora B assay efficiently detects endogenous Aurora B protein in various human cellular models expressing different levels of the protein.

HTRF Total Aurora B assay compared to Western Blot

HeLa cells were cultured in a T175 flask in complete culture medium at 37°C, 5% CO2. After 24H incubation, the cells were first stimulated with Nocodazole 300 nM for 20H, 37°C, 5% CO2, then lysed with 3 mL of supplemented lysis buffer #1 (1X) for 30 minutes at RT under gentle shaking.

Serial dilutions of the cell lysate were performed using supplemented lysis buffer, and 16 µL of each dilution were transferred into a low volume white microplate before the addition of 4 µL of HTRF Total Aurora B detection reagents. Equal amounts of lysates were used for a side by side comparison between HTRF and Western Blot.

A side by side comparison of Western Blot and HTRF demonstrates that the HTRF assay is 4-fold more sensitive than the Western Blot, at least under these experimental conditions.