An important contributing factor for the high sensitivity of sensory systems is the exquisite sensitivity of the sensory receptor cells. We report here the signaling threshold of the olfactory receptor neuron (ORN). We first obtained a best estimate of the size of the physiological electrical response successfully triggered by a single odorantbinding event on a frog ORN, which was ∼0.034 pA and had an associated transduction domain spanning only a tiny fraction of the length of an ORN cilium. We also estimated the receptor-current threshold for an ORN to fire action potentials in response to an odorant pulse, which was ∼1.2 pA. Thus, it takes about 35 odorantbinding events successfully triggering transduction during a brief odorant pulse in order for an ORN to signal to the brain.olfaction | olfactory transduction | sensory transduction O ur visual system has pushed to the physical limit of sensitivity. Thus, a dark-adapted human subject can report light when just a few photons are absorbed in a retinal area spanning hundreds of rod photoreceptors, suggesting that each dark-adapted rod can signal the absorption of a single photon (1). What about the olfactory system? How many odorant molecules have to bind to an olfactory receptor neuron (ORN) to trigger an output signal? Retinal rods lack axons, so a graded, light-induced change in membrane potential directly modulates synaptic transmission. In contrast, ORNs have axons and require action potentials to convey olfactory signals to the brain. Hence, the question becomes: How many odorant-binding events successfully triggering transduction are required for changing an ORN's firing?The canonical mechanism of olfactory transduction in the main olfactory epithelium is now quite well understood (2-5). Odorant receptors (ORs) on ORN cilia are G protein-coupled-receptors (6) that, upon binding specific odorants, activate the adenylyl cyclase type-III via the G protein, G olf . The ensuing rise in cAMP opens a cyclic-nucleotide-gated (CNG), nonselective cation channel to produce a membrane depolarization. Additionally, the Ca 2+ influx through the CNG channels opens a Ca 2+ -activated Cl channel on the ciliary membrane (7,8). The resulting Cl − flux is, however, outward (i.e., inward Cl current) because of a high intracellular Cl − concentration maintained by steady Cl − uptake via a Na/K/Cl cotransporter, NKCC1 (9-12, but see 13), thus further depolarizing the cell to provide amplification (9, 10). Simultaneously, the Ca 2+ influx triggers, via Ca 2+ -calmodulin, multiple negative-feedback pathways that lead to adaptation (2-5). Finally, action-potential generation in ORNs involves voltage-gated Na channels and lowvoltage-activated (T-type) Ca channels, at least near threshold (14). Previously, we have found surprisingly that most odorant-binding events on an ORN are actually "inconsequential": that is, unsuccessful in triggering transduction, apparently because the odorant-OR complex typically exists too briefly to activate the downstream pathway (15). The events descr...