The sulphhydryl environment in various mixed-metal hybrid hemoglobins, viz. α 2 (Cu)β 2 (FeCO), α 2 (FeCO)-β 2 (Cu), α 2 (Cu)-β 2 (Ni), α 2 (Ni)-β 2 (Cu), was studied by reacting them with the sulphhydryl reagent, 4,4′-dithiodipyridine (4-PDS). The reactivity was compared with that of HbCO, NiHb and CuHb. It is found that there exists a correlation between conformational change and metal ion environment, not only at the extreme R and T states but also the intermediate conformations. EPR examinations of these hybrids show that both in R state-[Cu(II)-Fe(II)] and T state-[Cu(II)-Ni(II)] hybrids at neutral pH and in the absence of IHP, CuPPIX, irrespective of the subunit in which it is present, has a mixed-metal ion environment: Species 1, a five-coordinated Cu 2+ complex with strong proximal histidine bond and species 2, a four-coordinated complex without any covalent linkage with Nε F8-histidine.