(A) cAMP-induced currents of an inside-out excised membrane patch from the dendritic knob of a wild type OSN (left) and a CNGB1^ΔCaM OSN (right). Patches were perfused with increasing concentrations of cAMP.
(B) cAMP dose-response relations of the wild type and CNGB1^ΔCaM channels. Current values were obtained by averaging from a time point when a steady state was reached (typically 0.5 - 1 second) to the end of cAMP exposure (12 seconds). Solid lines represent Hill curves fitted to the data. The wild type and CNGB1^ΔCaM channels have virtually identical cAMP dose-response relations. Wild type channel K_1/2, 3.11±0.02 μM (mean±SEM, n=7); CNGB1^ΔCaM channel K_1/2, 3.30±0.07 μM (n=7). Inset, the averaged steady-state currents induced by a saturating concentration of cAMP (100 μM). Wild type, 216±62 pA (mean±SEM, n=8); CNGB1^ΔCaM, 215±41 pA (n=20).
(C) Patches excised from wild type (upper panel) and CNGB1^ΔCaM (lower panel) OSNs were exposed to 6 μM of cAMP (the concentration corresponding to 0.75 open probability). The black trace represents the current evoked by cAMP in the absence of CaM. Application of CaM (red traces) quickly reduced the CNG current in patches from wild type OSNs, while causing only a slow reduction in patches from CNGB1^ΔCaM OSNs. The decay in wild type patches could be fitted with paired exponentials with average time constants of 0.78±0.42 seconds for the fast phase and 37±15 seconds (mean±SEM, n=4) for the slow phase. In CNGB1^ΔCaM patches, only a single exponential was fitted with an average time constant of 97±60 seconds (n=4). All experiments were performed in symmetrical Na-methanesulfonate solution (see Methods), and the pipette solution contained 1 mM niflumic acid to suppress the Ca²⁺-activated Cl^- current.

(A and B) EOG analysis.
(A) Left panel: Normalized EOG signals to two consecutive 100 ms pulses of vapor of 10^-4 M amyl acetate solution with 1-second interpulse intervals. The traces of the wild type (black) and CNGB1^ΔCaM (red) mice, each the average from 6 animals, are superimposed. The dashed lines represent traces obtained by fitting the termination phase with a single exponential equation. Right panel: traces represent the averaged “net” response to each stimulus. Since the responses have not returned to the baseline when the second stimulus is given, for each recording the “net” response caused by the second stimulus is calculated by subtracting the trace obtained by fitting the termination phase of the first response (illustrated by the dashed line in the left panel) from the trace of the second pulse.
(B) The net peak response ratios for amyl acetate (left) and heptaldehyde (right). CNGB1^ΔCaM OSNs exhibit comparable extent of adaptation to the wild type OSNs.
(C and D) Single cell analysis.
(C) Suction electrode recordings from an isolated wild type or CNGB1^ΔCaM OSN exposed twice to IBMX (1 mM, 1 second) with increasing interpulse intervals. Bottom panel: the ratios of the peak responses (second/first) are plotted against the interpulse time. Each data point is the average of 20 – 54 experiments, error bars represent SEM.
(D) Same experimental paradigm as in (C), but responses were evoked with 100 μM of cineole. Bottom panel: averaged results of 4 – 8 experiments.

Suction pipette recordings from an isolated wild type (top panel) or CNGB1^ΔCaM OSN (middle panel) in response to two IBMX pulses (1 mM, 1 second) separated by a 0.25 second interpulse interval. Traces were filtered with the wide bandwidth of DC – 5000 Hz to monitor action potential firing. Inset in the top panel shows the action potential events during the rising phase of the wild type OSN response to the second pulse on an expanded time scale. Note the lack of action potential events in the CNGB1^ΔCaM OSN response to the second pulse. Bottom panel: Percentage of OSNs firing action potentials as a function of the interpulse interval. Inset shows the three shortest interpulse intervals on an expanded time axis. Percentage of cells firing action potentials is statistically different at the 0.25 second interpulse interval (“*”, Chi-square test, p=0.0068). Values are mean ± 95% confidence interval and averages of 19 – 49 OSNs.

(A) Normalized EOG signals to a 20-second pulse of vapor of 10^-4 M amyl acetate solution. The EOG traces of the wild type (black) and CNGB1^ΔCaM (red) mice, each the average of recordings from 5 animals, are superimposed to show the attenuated adaptation of the CNGB1^ΔCaM mice during the stimulation. Note that our odorant delivery setup does not deliver a constant odorant concentration as the saturated vapor is diluted during the stimulation period. To assess how the concentration decrease affects the decline of EOG signals, we used a three-way valve to initially divert the odorant stream away from the epithelium and then towards the epithelium at different time points of the 20-second stimulation period. The peak amplitudes obtained are plotted as small open circles fit with an approximating dashed line. The presence of this concentration decrease should affect the tau values in (B). The tau is expected to be larger without this decrease in odorant concentration. Inset, EOG signals plotted from 0 to 2 seconds to show the longer rise time in CNGB1^ΔCaM OSNs. The arrows indicate the peak of the response.
(B) CNGB1^ΔCaM OSNs display slower response decline during sustained stimulation. The decline phase of EOG signals during the stimulation was fit with a single exponential. * p<0.01, Student t-test.
(C) CNGB1^ΔCaM OSNs have longer rise times in response to sustained stimulations. *, p<0.01.

(A) Generation of CNGB1^ΔCaM mice. The left and the right panel are schematics of the CNGB1b protein structure and a portion of the Cngb1 gene in the wild type and CNGB1^ΔCaM mice respectively. On the upper left, the N-terminal CaM-binding domain containing 20 amino acids in the CNGB1b protein is represented with a solid red circle. The transmembrane domains are depicted as yellow boxes and the cAMP-binding domain is represented as a green bar. Below, the exons of the Cngb1 gene are shown as open boxes. The targeting construct is illustrated at the bottom. K, KpnI; H, HindIII; S, SpeI; Bs, BstEII; Solid triangles, loxP sites. On the right, the mutant CNGB1b protein lacks the CaM-binding domain. The mutated exon in the Cngb1 gene is represented by the black box and the loxP site remaining in the intron is marked by the solid triangle.
(B) PCR analysis of genomic DNA across the deletion site. The precise elimination of the 60 nucleotides encoding 20 amino acid CaM-binding domain in the PCR products of CNGB1^ΔCaM mice were confirmed by sequencing.
(C) Western blot analysis of total OE proteins. CNGB1b, CNGA2, CNGA4, and ACIII are expressed at similar levels in wild type and CNGB1b^ΔCaM mice. α-tubulin is used as the loading control.
(D) Immunohistostaining of OE sections. CNGB1b, CNGA2, CNGA4, ACIII and PDE1C are all primarily detected at the cilial layer of the OE in both wild type and CNGB1b^ΔCaM mice. C, cilial layer; S, supporting cell layer; OSN, olfactory sensory neuron layer; BL, basal lamina, marked by a white dashed line. Scale bar: 20 μm.

(A) Averaged EOG amplitudes (n=6 mice, error bars represent SD) to a 100 ms pulse of vapor of a bottle containing 10^-4 M amyl acetate solution from eleven different locations along turbinate IIb and III. These locations are indicated in the photograph. D, dorsal; A, anterior.
(B) Dose-response relations for amyl acetate. The epithelium was exposed to 100 ms pulses of vapor of increasing concentration of amyl acetate solution. The concentrations marked on the X-axis are the solution concentrations in the bottle. The data points (n=6 mice, error bars represent SD) are linked with straight line. The EOG signals were recorded from location 1.

(A and B) EOG analysis.
(A) Normalized EOG signals to a 100 ms pulse of vapor of 10^-4 M amyl acetate. The EOG traces of wild type (black) and CNGB1^ΔCaM (red) mice, each the average from 6 animals, are superimposed to show the slower termination phase of CNGB1^ΔCaM mice.
(B) Time constants of the termination phase. The termination phase (100% – 10% peak) of each response was fitted with a single exponential. *, p<0.05 for 10^-4 M; p<0.01 for 10^-3 M and 10^-2 M (Student’s t-test).
(C – G) Single cell suction electrode recordings in response to a 1-second IBMX exposure. Examples of a wild type OSN (black) and a CNGB1^ΔCaM OSN (red) are shown in (C). Collected results from multiple recordings are shown in (D – G).
(D) The difference in the peak current between the two genotypes is not significant (NS, p=0.05 Student’s t-test). The number of recordings is provided in parenthesis below the graphs.
(E) In CNGB1^ΔCaM OSNs, the time for the current to decline to 20% of the end-perfusion value is significantly longer, meaning slower termination kinetics (*, p<0.01).
(F) Consistent with the EOG data (see Figure 8B), CNGB1^ΔCaM OSNs retained significantly larger currents at the end of stimulation compared to wild type, meaning attenuated adaptation (*, p<0.05).
(G) Consistent with the EOG data (see Figure 8C), CNGB1^ΔCaM OSNs have a longer time to peak in response to sustained stimulation (*, p<0.01).

(A) Experimental setup for odor stimulation and assessment of field responses in the OB. The recording electrode was positioned in the deep layer of the OB. (B) Two consecutive odor pulses were delivered at the same phase of the breathing cycle. This was achieved in real-time by triggering the olfactometer from piezoelectric sensor attached to the animals’ chest. (C and D) Series of representative odor-evoked local field potentials (LFPs) recorded from the OB of the wild type (C) and CNGB1^ΔCaM (D) mice to paired odor pulses separated by 1, 2, 3 and 6 breathing cycles (approximate 0.3, 0.6, 1.0 and 2.0 sec ISI). The triangles denote the start of the first (filled) and the second (open) odor pulses. (E) The average paired-pulse ratios R2/R1 as a function of ISIs for odor-evoked responses (peak amplitude) in the wild type (black squares) and CNGB1^ΔCaM mice (red circles). Each point is an average response from 5 animals in each experimental group ±SE. In each animal, the odor responses are averaged over 5 repetitions. Solid lines represent a single exponential fit to the paired-pulse ratios. Inset shows the four shortest ISI points on an expanded time axis. P values obtained using Student’s t-test. (F). Average time constant of LFP recovery (wild type, 0.35±0.042 sec; CNGB1^ΔCaM, 0.50±0.048 sec). p=0.045, Student’s t-test.