HTRF Human Phospho-eNOS (Ser1177) Detection Kit, 500 Assay Points

Phospho-eNOS (Ser1177) assay principle

The Phospho-eNOS (S1177) assay measures eNOS when phosphorylated at serine 1177. Unlike Western Blot, the assay is entirely plate-based and does not require gels, electrophoresis, or transfer. The assay uses 2 antibodies, one labeled with a donor fluorophore and the other with an acceptor. The first antibody is selected for its specific binding to the phosphorylated motif on the protein, the second for its ability to recognize the protein independently of its phosphorylation state. Protein phosphorylation enables an immune-complex formation involving both labeled antibodies, and which brings the donor fluorophore into close proximity to the acceptor, thereby generating a FRET signal. Its intensity is directly proportional to the concentration of phosphorylated protein present in the sample, and provides a means of assessing the protein's phosphorylation state under a no-wash assay format.

Phospho-eNOS (Ser1177) two-plate assay protocol

The two-plate protocol involves culturing cells in a 96-well plate before lysis, then transferring lysates to a 384-well low volume detection plate before the addition of Phospho-eNOS (Ser1177) HTRF detection reagents. This protocol enables the cells' viability and confluence to be monitored.

Phospho-eNOS (Ser1177) one-plate assay protocol

Detection of Phosphorylated eNOS (Ser1177) 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.

Serum starvation and phosphorylation accumulation

Huvec cells were seeded in a 160mm Petri Dish at 80% of confluence in 37°C, 5% Co2 conditions, and an overnight serum starvation was done or not. Then a solution of pervanadate at 30µM for 30 minutes was added or not. Lysis buffer was added to each dish after culture medium removal, and incubated for 30 minutes under shaking. Then 16µl of lysate were transferred into a 384 well plate for Total and Phospho Ser1177 eNOS detection.

Starvation seems to induce a slight decrease in protein, but a real decrease in the phosphorylation level. Phosphorylation accumulation with pervanadate is efficient.

eNOS phosphorylation induced by fenofibrate stimulation through AMPK pathway

Huvec cells were seeded in a 100mm Petri Dish at 80% of confluence in 37°C, 5% Co2 conditions, and an overnight serum starvation was done. Then a fenofibrate solution at 30µM was added for 30 minutes or not. Lysis buffer was then dispensed after culture medium removal. 16µl of lysate were transferred into a 384 well plate for Total and Phospho Ser1177 eNOS detection.

WB versus HTRF assay for phospho-eNOS (Ser1177)

Huvec cells were grown in a 160mm Petri dish at 37°C, 5% Co2, for 2 days. Overnight serum starvation was carried out before an incubation of pervanadate at 30µM for 30 min. After removal of cell culture medium, 3 mL of supplemented lysis buffer were added and incubated for 30 min. Soluble supernatants were collected after 10 min centrifuging. Equal amounts of lysates were used for a side by side comparison of WB and HTRF. Phospho-eNOS (Ser1177)assay shows a better sensitivity than Western Blot: 37,500 cells/mL are sufficient to be detected by HTRF, while WB needs 75,000.