Early detection of Alzheimer’s
disease (AD) is
important
for taking proper measures against AD pathogenesis. Acetylcholinesterase
(AChE) is widely reported to be associated with the pathogenicity
of AD. Here, employing the “acetylcholine-mimic” approach,
we designed and synthesized a new class of naphthalimide (Naph)-based
fluorogenic probes for specific detection of AChE and avoiding interference
of butyrylcholinesterase (BuChE), the pseudocholinesterase. We investigated
the action of the probes on Electrophorus electricus AChE, and the native human brain AChE that we expressed in Escherichia coli and purified in the active form
for the first time. The probe Naph-3 exhibited a substantial
fluorescence enhancement with AChE and majorly avoided BuChE. Naph-3 successfully crossed the cell membrane of the Neuro-2a
cells and fluoresced upon reaction with endogenous AChE. We further
established that the probe could be effectively used for screening
AChE inhibitors. Our study provides a new avenue for the specific
detection of AChE, which can be extended to the diagnosis of AChE-related
complications.
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