Table 1.
Role of the effector and insert regions of Rac in the hysteretic coupling of the Rac redox response and NOX2 activation
| Rac | Hyperbolic NOX2 activation with fully preactivated Rac | Hysteretic Rac activation with initially inactive Rac | Hysteretic NOX2 activation with initially inactive Rac | Hyperbolic Rac activation with fully preactivated Rac | Rac redox sensitivitya | |
|---|---|---|---|---|---|---|
| wt Rac | +++ | +++ | +++ | +++ | +++ | |
| Rac redox motif mutants | C18S | — | — | — | +++ | — |
| C157S | — | — | — | +++ | — | |
| Rac effector region mutants | A27K | — | — | — | — | +++ |
| G30S | — | — | — | — | +++ | |
| Rac insert region mutants | K132E | ++ | ++ | ++ | ++ | +++ |
| L134R | ++ | ++ | ++ | ++ | +++ | |
Rac redox sensitivity was measured without the NOX2 phox complex in the cell-free system by using KO2 as the O2− source. The symbol “+++” represents the maximal wt Rac redox sensitivity or the fastest hysteretic activation rate of NOX2 and wt Rac over time based upon the results shown in Figure 2, A and B. The symbols “++” and “+” reflect, respectively, 30% and 60% slower rates than those of the rates shown as “+++.” The symbol “—” denotes a lack of the redox sensitivity or hysteretic activation over time.