PT  - JOURNAL ARTICLE
AU  - Ayman K. Hamouda
AU  - Farah Deba
AU  - Ze-Jun Wang
AU  - Jonathan B. Cohen
TI  - Photolabeling a Nicotinic Acetylcholine Receptor (nAChR) with an (&lt;em&gt;α&lt;/em&gt;4)&lt;sub&gt;3&lt;/sub&gt;(&lt;em&gt;β&lt;/em&gt;2)&lt;sub&gt;2&lt;/sub&gt; nAChR-Selective Positive Allosteric Modulator
AID  - 10.1124/mol.116.103341
DP  - 2016 May 01
TA  - Molecular Pharmacology
PG  - 575--584
VI  - 89
IP  - 5
4099  - http://molpharm.aspetjournals.org/content/89/5/575.short
4100  - http://molpharm.aspetjournals.org/content/89/5/575.full
SO  - Mol Pharmacol2016 May 01; 89
AB  - Positive allosteric modulators (PAMs) of nicotinic acetylcholine (ACh) receptors (nAChRs) have potential clinical applications in the treatment of nicotine dependence and many neuropsychiatric conditions associated with decreased brain cholinergic activity, and 3-(2-chlorophenyl)-5-(5-methyl-1-(piperidin-4-yl)-1H-pyrrazol-4-yl)isoxazole (CMPI) has been identified as a PAM selective for neuronal nAChRs containing the α4 subunit. In this report, we compare CMPI interactions with low-sensitivity (α4)3(β2)2 and high-sensitivity (α4)2(β2)3 nAChRs, and with muscle-type nAChRs. In addition, we use the intrinsic reactivity of [3H]CMPI upon photolysis at 312 nm to identify its binding sites in Torpedo nAChRs. Recording from Xenopus oocytes, we found that CMPI potentiated maximally the responses of (α4)3(β2)2 nAChR to 10 μM ACh (EC10) by 400% and with an EC50 of ∼1 µM. CMPI produced a left shift of the ACh concentration-response curve without altering ACh efficacy. In contrast, CMPI inhibited (∼35% at 10 µM) ACh responses of (α4)2(β2)3 nAChRs and fully inhibited human muscle and Torpedo nAChRs with IC50 values of ∼0.5 µM. Upon irradiation at 312 nm, [3H]CMPI photoincorporated into each Torpedo [(α1)2β1γδ] nAChR subunit. Sequencing of peptide fragments isolated from [3H]CMPI-photolabeled nAChR subunits established photolabeling of amino acids contributing to the ACh binding sites (αTyr190, αTyr198, γTrp55, γTyr111, γTyr117, δTrp57) that was fully inhibitable by agonist and lower-efficiency, state-dependent [3H]CMPI photolabeling within the ion channel. Our results establish that CMPI is a potent potentiator of nAChRs containing an α4:α4 subunit interface, and that its intrinsic photoreactivy makes it of potential use to identify its binding sites in the (α4)3(β2)2 nAChR.