The PDE5A1 Assay Kit is designed for identification of PDE5A1 inhibitors using fluorescence polarization. The assay is based on the binding of a fluorescent nucleotide monophosphate generated by PDE5A to the binding agent. PDE5A catalyzes the hydrolysis of the phosphodiester bond in dye-labeled cyclic guanosine monophosphate. Nanoparticle beads selectively bind the phosphate group in the nucleotide product. This increases the size of the nucleotide relative to unreacted cyclic guanosine monophosphate. In the polarization assay, dye molecules with absorption transition vectors parallel to the linearlypolarized excitation light are selectively excited. Dyes attached to the rapidly-rotating cyclic monophosphates will obtain random orientations and emit light with low polarization. Dyes attached to the slowly-rotating nucleotide-bead complexes will not have time to reorient and therefore will emit highly polarized light. The key to the PDE5A1 Assay Kit is the specific binding agent. Using this kit, only two simple steps on a microtiter plate are required for PDE5A1 reactions. First, the fluorescently labeled cGMP is incubated with a sample containing PDE5A1 for 1 hour. Second, a binding agent is added to the reaction mix to produce a change in fluorescent polarization that can then be measured using a fluorescence reader.

Fluorescent microplate reader capable of measuring fluorescence polarization

PDE5A, phosphodiesterase 5A

The PDE5A1 inhibitor screening assay kit comes in a convenient 384-well format, including purified PDE5A1 enzyme, fluorescently labeled PDE5A1 substrate (cGMP), binding agent, and PDE assay buffer for 384 enzyme reactions.

See datasheet for detailed protocol.

6 months from date of receipt when stored as directed

Great for studying enzyme kinetics and screening small molecular inhibitors for drug discovery and HTS applications.

Maurice DH. Front. Biosci. 2005; 10:1221-8.

Avoid freeze/thaw cycles

Phosphodiesterase

Assay Kit