Probing Binding Interactions of Cytisine Derivatives to the α4β2 Nicotinic Acetylcholine Receptor
journal contributionposted on 2019-09-24, 18:42 authored by Annet E.M. Blom, Hugo Rego Campello, Henry A. Lester, Timothy Gallagher, Dennis A. Dougherty
Nicotinic acetylcholine receptors (nAChRs) are crucial for communication between synapses in the central nervous system. As such, they are also implicated in several neuropsychiatric and addictive diseases. Cytisine is a partial agonist of some nAChRs and has been used for smoking cessation. Previous studies have established a binding model for several agonists to several nAChR subtypes. Here, we evaluate the extent to which this model applies to cytisine at the α4β2 nAChR, which is a subtype that is known to play a prominent role in nicotine addiction. Along with the commonly seen cation−π interaction and two hydrogen bonds, we find that cytisine makes a second cation−π interaction at the agonist binding site. We also evaluated a series of C(10)-substituted cytisine derivatives, using two-electrode voltage-clamp electrophysiology and noncanonical amino acid mutagenesis. Double-mutant cycle analyses revealed that C(10) substitution generally strengthens the newly established second cation−π interaction, while it weakens the hydrogen bond typically seen to LeuE in the complementary subunit. The results suggest a model for how cytisine derivatives substituted at C(10) (as well as C(9)/C(10)) adjust their binding orientation, in response to pyridone ring substitution.
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nAChR subtypesbinding modelcationα4β2 nAChRnicotine addictionPrevious studiesagonist binding sitesmoking cessationCytisine Derivativeshydrogen bondsacid mutagenesisDouble-mutant cycle analysesbinding orientationinteractiontwo-electrode voltage-clamp electrophysiologypyridone ring substitutionhydrogen bondcytisine derivativesα4β2 Nicotinic Acetylcholine Receptor Nicotinic acetylcholine receptorsBinding Interactions