Table 1.
Temperature | Agonist | Treatment | pKHa | pKLb | FHc | nHd | ne |
---|---|---|---|---|---|---|---|
25°C | R-PIA | ADAf | 8.82±0.08g | 6.42±0.13 | 0.68±0.03 | 0.54±0.03h | 3 |
Gpp(NH)pi | 7.72±0.06g | 6.42±0.13 | 0.68±0.03 | 0.72±0.05h | 3 | ||
Ureaj | 7.71±0.06 | 6.42±0.13 | 0.68±0.03 | 0.63±0.04h | 3 | ||
CHA | ADA | 8.64±0.09 | 6.15±0.19 | 0.69±0.04 | 0.52±0.05h | 3 | |
Gpp(NH)p | 7.21±0.08 | 6.15±0.19 | 0.69±0.04 | 0.77±0.08h | 3 | ||
Urea | ND | 6.15±0.19 | NA | 1.17±0.13 | 3 | ||
37°C | R-PIA | ADA | 8.00±0.23 | 6.39±0.20 | 0.51±0.11 | 0.63±0.07h | 3 |
Gpp(NH)p | 7.16±0.14 | 6.39±0.20 | 0.51±0.11 | 1.05±0.14 | 3 | ||
Urea | ND | 6.39±0.20 | NA | 1.17±0.17 | 3 | ||
CHA | ADA | 8.22±0.14 | 6.37±0.14 | 0.54±0.06 | 0.55±0.05h | 3 | |
Gpp(NH)p | 7.08±0.12 | 6.37±0.14 | 0.54±0.06 | 0.80±0.09h | 3 | ||
Urea | ND | 6.37±0.14 | NA | 0.95±0.06 | 3 | ||
Adenosine | Urea | ND | 5.66±0.05 | NA | 0.98±0.09 | 3 |
Assays were performed for 90 min in 50 mM Tris(HCl) buffer at the indicated temperatures. Nonspecific binding was defined using 10 μM R-PIA.
Negative logarithm of the apparent dissociation constant for the high-affinity agonist-binding state, determined by global nonlinear regression analysis of all three treatment groups to a common binding model (see Methods).
Negative logarithm of the apparent dissociation constant for the low-affinity agonist-binding state, determined by global nonlinear regression analysis of all three treatment groups to a common binding model. An extra-sum-of squares (F-test) concluded that a single value of the parameter could describe all the curves.
Fraction of the high-affinity agonist-binding state, determined by global nonlinear regression analysis of all three treatment groups to a common binding model. An extra-sum-of squares (F-test) concluded that a single value of the parameter could describe all the curves where a high-affinity state was evident.
Hill slope, determined by nonlinear regression analysis to a logistic function.
Number of experiments.
Membranes were pretreated with 10 U ml−1 ADA during preparation, and assays subsequently performed in the presence of 0.1 U ml−1 ADA.
Significantly different (P<0.05; Student's t-test) from the corresponding value at 37°C.
Significantly different (P<0.05; F-test) from 1.
As in footnote f above, but with the addition of 100 μM Gpp(NH)p.
Membranes were pretreated with 7 M urea during preparation.
ND, not determined.
NA, not applicable.