Cytochrome c peroxidase cytochrome c complex: Locating the second binding domain on cytochrome c peroxidase with site-directed mutagenesis

Cytochrome c peroxidase (CcP) can bind as many as two cytochrome c (Cc) mol ecules in an electrostatic complex. The location of the two binding domains on CcP has been probed by photoinduced interprotein electron transfer (ET) between zinc-substituted horse cytochrome c (ZnCc) and CcP with surface ch arge-reversal mutations and by isothermal titration calorimetry (ITC). Thes e results, which are the first experimental evidence for the location of do main 2, indicate that the weak-binding domain includes residues 146-150 on CcP. CcP(E290K) has a charge-reversal mutation in the tight-binding domain, which should weaken binding, and it weakens the 1:1 complex; K-1 decreases 20-fold at 18 mM ionic strength. We have employed two mutations to probe t he proposed location for the weak-binding domain on the CcP surface: (i) D1 48K, a "detrimental" mutation with a net (+2) change in the charge of CcP, and (ii) K149E, a "beneficial" mutation with a net (-2) change in the charg e. The interactions between FeCe and CcP(WT and K149E) also have been studi ed with ITC. The CcP(D148K) mutation causes no substantial change in the 2: 1 binding but an increase in the reactivity of the 2:1 complex. The latter can be interpreted as a long-range influence on the heme environment or, mo re likely, the enhancement of a minority subset of binding conformations wi th favorable pathways for ET. CcP(K149E) has a charge-reversal mutation in the weak-binding domain that produces a substantial increase in the 2:1 bin ding constant as measured by both quenching and ITC. For the 1:1 complex of CcP(WT), Delta G(1) = -8.2 kcal/mol (K-1 = 1.3 x 10(6) M-1), Delta H-1 = 2.7 kcal/mol, and Delta S-1 = +37 cal/K.mol at 293 K; for the second bindin g stage, K-2 < 5 x 10(3) M-1, but accurate thermodynamic parameters were no t obtained. For the 1:1 complex of CcP(K149E), Delta G(1) = -8.5 kcal/mol ( K-1 = 2 x 10(6) M-1), Delta H-1 = +2.0 kcal/mol, and Delta S-1 = +36 cal/K. mol; for the second stage, Delta G(2) = -5.5 kcal/mol (K-1 = 1.3 x 10(4) M- 1), Delta H-2 = +2.9 kcal/mol, and Delta S-2 +29 cal/K.mol.