TABLE 1.
CD200R |
KD (μM)
|
koff
|
||||
---|---|---|---|---|---|---|
Host CD200 | Viral K14 | Host CD200
|
Viral K14
|
|||
s−1 | t1/2 (s) | s−1 | t1/2 (s) | |||
Human | 0.49 ± 0.08 | 0.49 ± 0.09 | 0.09 ± 0.004 | 7.7 | 0.11 ± 0.008 | 6.1 |
Rat | 0.59 ± 0.07 | 0.67 ± 0.07 | 0.24 ± 0.03 | 2.9 | 0.17 ± 0.03 | 4.1 |
Mouse | 7.0 ± 0.33 | 9.2 ± 0.98 | 2.10 ± 0.2 | 0.3 | 1.7 ± 0.3 | 0.4 |
The KD values were determined by averaging those calculated from each of the three different CD200R immobilization levels obtained by nonlinear curve fitting (note that the curves shown in Fig. 2B are from high levels of human CD200R immobilization alone). The koff values were determined by averaging the values obtained by fitting the dissociation phases of the binding curves to a simple 1:1 binding model (see Materials and Methods), using two different concentrations of ligand over three levels of receptor immobilization (i.e., n = 6). In all cases, the level of receptor immobilization had negligible effects on koff, indicating that mass transport and rebinding effects were minimal. Data for CD200-CD200R interaction are from reference 42. Results are shown as means ± standard deviations.