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. 2005 Jan 13;563(Pt 2):345–358. doi: 10.1113/jphysiol.2004.080028

Table 3.

Kinetic parameters and least-squares fitting of macroscopic data

A Kinetic parameters Units NR1/NR2A NR1/NR2B % difference
10–90% rise time ms 7.4 ± 0.7 11.6 ± 1.2 − 36*
Deactivation ms 32.1 128 −75
τ1 (% area) (94%) (82%)
Deactivation ms 202 799 −75
τ2 (% area) (6%) (18%)
Desensitization ms 59.9 142 −58
τ1 (% area) (38%) (85%)
Desensitization ms 257 888 −71
τ2 (% area) (62%) (15%)
B Fitted rate constants Units NR1/NR2A NR1/NR2B % difference
kd1+ s−1 85.1 550 −85
kd1− s−1 29.7 81.4 −64
kd2+ s−1 230 112  105
kd2− s−1 1.01 0.91  11
kon μm−1 s−1 31.6 2.83 1017
koff s−1 1010 38.1 2551
Kd μm 32.0 13.5  137

A, 10–90% rise time measurements were made for individual patches (n = 18 for NR1/NR2A, n = 8 for NR1/NR2B; *P < 0.05). The deactivation or desensitization time course of mean waveforms was fitted to a double exponentially decaying function. B, fitting of macroscopic currents (see Fig. 5) to Scheme 4 with kf+, kf–, ks+, ks– fixed to values determined from single-channel data (Fig. 4 and Table 2) was used to determine binding and desensitization constants. Kd =koff/kon. Percentage difference is relative to the rate for the NR2B subunit. %diff = 100 × (2A–2B)/2B.