BioEssays

doi: 10.1002/bies.201370127pmid: N/A

doi: 10.1002/bies.201370125pmid: N/A

doi: 10.1002/bies.201370122pmid: N/A

doi: 10.1002/bies.201370121pmid: N/A

Moore, Andrew

doi: 10.1002/bies.201370123pmid: 24242096

doi: 10.1002/bies.201370126pmid: N/A

Hawrot, Edward

doi: 10.1002/bies.201300148pmid: 24242098

Keyes, William M.

doi: 10.1002/bies.201300157pmid: 24242099

Defossez, Pierre‐Antoine

doi: 10.1002/bies.201300151pmid: 24242100

Kabbani, Nadine; Nordman, Jacob C.; Corgiat, Brian A.; Veltri, Daniel P.; Shehu, Amarda; Seymour, Victoria A.; Adams, David J.

doi: 10.1002/bies.201300082pmid: 24185813

It was, until recently, accepted that the two classes of acetylcholine (ACh) receptors are distinct in an important sense: muscarinic ACh receptors signal via heterotrimeric GTP binding proteins (G proteins), whereas nicotinic ACh receptors (nAChRs) open to allow flux of Na+, Ca2+, and K+ ions into the cell after activation. Here we present evidence of direct coupling between G proteins and nAChRs in neurons. Based on proteomic, biophysical, and functional evidence, we hypothesize that binding to G proteins modulates the activity and signaling of nAChRs in cells. It is important to note that while this hypothesis is new for the nAChR, it is consistent with known interactions between G proteins and structurally related ligand‐gated ion channels. Therefore, it underscores an evolutionarily conserved metabotropic mechanism of G protein signaling via nAChR channels. Also watch the Video Abstract.