Literature DB >> 9341204

Site-directed mutants of pseudoazurin: explanation of increased redox potentials from X-ray structures and from calculation of redox potential differences.

C A Libeu1, M Kukimoto, M Nishiyama, S Horinouchi, E T Adman.   

Abstract

In order to understand the origins of differences in redox potentials among cupredoxins (small blue type I copper-containing proteins that reversibly change oxidation state and interact with redox partners), we have determined the structures of the native and two mutants (P80A and P80I) of pseudoazurin from Alcaligenes faecalis S-6 in oxidized and reduced forms at resolutions of 2.2 A in the worst case and 1.6 A in the best case. The P80A mutation creates a surface pocket filled by a new water molecule, whereas the P80I mutant excludes this water. Distinct patterns of change occur in response to reduction for all three molecules: the copper position shifts, Met 7 and Pro 35 move, and the relative orientations of residues 81 to 16, 18 to the amide planes of 77 and 86, all change. Systematic changes in the weak electrostatic interactions seen in the structures of different oxidation states can explain the Met 7/Pro 35 structural differences as well as some fluctuating solvent positions. Overall displacement parameters increase reversibly upon reduction. The reduced forms are slightly expanded over the oxidized forms. The geometries of the mutants become more trigonal in their reduced forms, consistent with higher redox potentials (+409 mV for P80A and +450 mV for P80I). Calculations of the differences in redox potentials, using POLARIS, reveal that a water unique to the P80A mutant is required (with correctly oriented hydrogens) to approximate the observed difference in redox potential. The POLARIS calculations suggest that the reduced forms are additionally stabilized through changes in the solvation of the copper center, specifically via the amides of residues 16, 39, 41, 79, and 80 which interact with either Phe 18, Met 86, or Cys 78. The redox potential of P80A is increased largely due to solvation effects, whereas the redox potential of P80I is increased largely due to geometrical effects.

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Year:  1997        PMID: 9341204     DOI: 10.1021/bi9704111

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  12 in total

1.  Stabilization of protein structure through π-π interaction in the second coordination sphere of pseudoazurin.

Authors:  Takahide Yamaguchi; Yuko Nihei; Duncan E K Sutherland; Martin J Stillman; Takamitsu Kohzuma
Journal:  Protein Sci       Date:  2017-07-20       Impact factor: 6.725

Review 2.  Metalloproteins containing cytochrome, iron-sulfur, or copper redox centers.

Authors:  Jing Liu; Saumen Chakraborty; Parisa Hosseinzadeh; Yang Yu; Shiliang Tian; Igor Petrik; Ambika Bhagi; Yi Lu
Journal:  Chem Rev       Date:  2014-04-23       Impact factor: 60.622

3.  Sequence determination of reduction potentials by cysteinyl hydrogen bonds and peptide pipoles in [4Fe-4S] ferredoxins.

Authors:  B W Beck; Q Xie; T Ichiye
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

4.  Blue copper proteins: a comparative analysis of their molecular interaction properties.

Authors:  F De Rienzo; R R Gabdoulline; M C Menziani; R C Wade
Journal:  Protein Sci       Date:  2000-08       Impact factor: 6.725

5.  New molecular packing in a crystal of pseudoazurin from Alcaligenes faecalis: a double-helical arrangement of blue copper.

Authors:  Yohta Fukuda; Eiichi Mizohata; Tsuyoshi Inoue
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2017-02-28       Impact factor: 1.056

Review 6.  Cupredoxins--a study of how proteins may evolve to use metals for bioenergetic processes.

Authors:  Moonsung Choi; Victor L Davidson
Journal:  Metallomics       Date:  2011-01-24       Impact factor: 4.526

7.  Zinc-substituted pseudoazurin solved by S/Zn-SAD phasing.

Authors:  Renate Gessmann; Maria Papadovasilaki; Evangelos Drougkas; Kyriacos Petratos
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-01-01       Impact factor: 1.056

8.  Metal-binding loop length and not sequence dictates structure.

Authors:  Katsuko Sato; Chan Li; Isabelle Salard; Andrew J Thompson; Mark J Banfield; Christopher Dennison
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-19       Impact factor: 11.205

9.  NMR hyperfine shifts in blue copper proteins: a quantum chemical investigation.

Authors:  Yong Zhang; Eric Oldfield
Journal:  J Am Chem Soc       Date:  2008-03-04       Impact factor: 15.419

10.  Hydrogen Bonds Dictate the Coordination Geometry of Copper: Characterization of a Square-Planar Copper(I) Complex.

Authors:  Eric W Dahl; Nathaniel K Szymczak
Journal:  Angew Chem Int Ed Engl       Date:  2016-01-28       Impact factor: 15.336

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