文摘
Using de novo protein design, we incorporated a copper metal binding site within the three-helix bundle 伪3D (Walsh et al. Proc. Natl. Acad. Sci. U.S.A. 1999, 96, 5486鈥?491) to assess whether a cupredoxin center within an 伪-helical domain could mimic the spectroscopic, structural, and redox features of native type-1 copper (CuT1) proteins. We aimed to determine whether a CuT1 center could be realized in a markedly different scaffold rather than the native 尾-barrel fold and whether the characteristic short Cu鈥揝 bond (2.1鈥?.2 脜) and positive reduction potentials could be decoupled from the spectroscopic properties (蔚600聽nm = 5000 M鈥?/b>1 cm鈥?/b>1) of such centers. We incorporated 2HisCys(Met) residues in three distinct 伪3D designs designated core (CR), chelate (CH), and chelate-core (ChC). XAS analysis revealed a coordination environment similar to reduced CuT1 proteins, producing Cu鈥揝(Cys) bonds ranging from 2.16 to 2.23 脜 and Cu鈥揘(His) bond distances of 1.92鈥?.99 脜. However, Cu(II) binding to the CR and CH constructs resulted in tetragonal type-2 copper-like species, displaying an intense absorption band between 380 and 400 nm (>1500 M鈥?/b>1 cm鈥?/b>1) and A|| values of (150鈥?85) 脳 10鈥?/b>4 cm鈥?/b>4. The ChC construct, which possesses a metal-binding site deeper in its helical bundle, yielded a CuT1-like brown copper species, with two absorption bands at 401 (4429 M鈥?/b>1 cm鈥?/b>1) and 499 (2020 M鈥?/b>1 cm鈥?/b>1) nm and an A|| value 鈭?0 脳 10鈥? cm鈥? greater than its native counterparts. Electrochemical studies demonstrated reduction potentials of +360 to +460 mV (vs NHE), which are within the observed range for azurin and plastocyanin. These observations showed that the designed metal binding sites lacked the necessary rigidity to enforce the appropriate structural constraints for a Cu(II) chromophore (EPR and UV鈥搗is); however, the Cu(I) structural environment and the high positive potential of CuT1 centers were recapitulated within the 伪-helical bundle of 伪3D.