Development of a High-throughput Assay to Identify Novel Reactivators of Acetylcholinesterase
Becky L. Hood, Stefan VasileiD, Gideon Shapiro, James D. Talton
Abstract
Acetylcholinesterase (AChE) is a key enzyme in the nervous system capable of breaking down acetylcholine (ACh). ACh is a critical neurotransmitter that signals between nerve cells and muscles. Organophosphates (OPs), used as insecticides and nerve agents, irreversibly inhibit AChE by forming a covalent bond with the enzymes active site. Since exposure to these nerve agents can quickly lead to death, many researchers have strived to discover new drugs that will reverse the inhibition of AChE by such agents. The goal was to develop a high-throughput miniaturized assay for testing large numbers of compounds for AChE reactivation quickly and reliably. Here we describe our miniaturized assay that utilizes the sarin surrogate nitrophenyl isopropyl methylphosphonate (NIMP) in an Amplex Red coupled assay and its validation with 42 compounds selected from an in silico virtual screen.
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