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. 1998 Dec;7(12):2659–2668. doi: 10.1002/pro.5560071220

Quantum chemical calculations of the reorganization energy of blue-copper proteins.

M H Olsson 1, U Ryde 1, B O Roos 1
PMCID: PMC2143893  PMID: 9865961

Abstract

The inner-sphere reorganization energy for several copper complexes related to the active site in blue-copper protein has been calculated with the density functional B3LYP method. The best model of the blue-copper proteins, Cu(Im)2(SCH3)(S(CH3)2)(0/+), has a self-exchange inner-sphere reorganization energy of 62 kJ/mol, which is at least 120 kJ/mol lower than for Cu(H2O)4(+/2+). This lowering of the reorganization energy is caused by the soft ligands in the blue-copper site, especially the cysteine thiolate and the methionine thioether groups. Soft ligands both make the potential surfaces of the complexes flatter and give rise to oxidized structures that are quite close to a tetrahedron (rather than tetragonal). Approximately half of the reorganization energy originates from changes in the copper-ligand bond lengths and half of this contribution comes from the Cu-S(Cys) bond. A tetragonal site, which is present in the rhombic type 1 blue-copper proteins, has a slightly higher (16 kJ/mol) inner-sphere reorganization energy than a trigonal site, present in the axial type 1 copper proteins. A site with the methionine ligand replaced by an amide group, as in stellacyanin, has an even higher reorganization energy, about 90 kJ/mol.

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Selected References

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  1. Adman E. T. Copper protein structures. Adv Protein Chem. 1991;42:145–197. doi: 10.1016/s0065-3233(08)60536-7. [DOI] [PubMed] [Google Scholar]
  2. Farver O., Pecht I. Blue copper proteins as a model for investigating electron transfer processes within polypeptide matrices. Biophys Chem. 1994 May;50(1-2):203–216. doi: 10.1016/0301-4622(94)85032-1. [DOI] [PubMed] [Google Scholar]
  3. Guss J. M., Bartunik H. D., Freeman H. C. Accuracy and precision in protein structure analysis: restrained least-squares refinement of the structure of poplar plastocyanin at 1.33 A resolution. Acta Crystallogr B. 1992 Dec 1;48(Pt 6):790–811. doi: 10.1107/s0108768192004270. [DOI] [PubMed] [Google Scholar]
  4. Guss J. M., Harrowell P. R., Murata M., Norris V. A., Freeman H. C. Crystal structure analyses of reduced (CuI) poplar plastocyanin at six pH values. J Mol Biol. 1986 Nov 20;192(2):361–387. doi: 10.1016/0022-2836(86)90371-2. [DOI] [PubMed] [Google Scholar]
  5. Holm Richard H., Kennepohl Pierre, Solomon Edward I. Structural and Functional Aspects of Metal Sites in Biology. Chem Rev. 1996 Nov 7;96(7):2239–2314. doi: 10.1021/cr9500390. [DOI] [PubMed] [Google Scholar]
  6. Ryde U., Olsson M. H., Pierloot K., Roos B. O. The cupric geometry of blue copper proteins is not strained. J Mol Biol. 1996 Aug 30;261(4):586–596. doi: 10.1006/jmbi.1996.0484. [DOI] [PubMed] [Google Scholar]
  7. Soriano G. M., Cramer W. A., Krishtalik L. I. Electrostatic effects on electron-transfer kinetics in the cytochrome f-plastocyanin complex. Biophys J. 1997 Dec;73(6):3265–3276. doi: 10.1016/S0006-3495(97)78351-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Williams R. J. Energised (entatic) states of groups and of secondary structures in proteins and metalloproteins. Eur J Biochem. 1995 Dec 1;234(2):363–381. doi: 10.1111/j.1432-1033.1995.363_b.x. [DOI] [PubMed] [Google Scholar]

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