4K9J

Structure of Re(CO)3(4,7-dimethyl-phen)(Thr126His)(Lys122Trp)(His83Glu)(Trp48Phe)(Tyr72Phe)(Tyr108Phe)AzCu(II), a Rhenium modified Azurin mutant

Summary for 4K9J

• Entry DOI: 10.2210/pdb4k9j/pdb
• Related: 4AZU
• Descriptor: Azurin, COPPER (II) ION, (1,10 PHENANTHROLINE)-(TRI-CARBON MONOXIDE) RHENIUM (I), ... (4 entities in total)
• Functional Keywords: electron transport, rhenium
• Biological source: Pseudomonas aeruginosa
• Cellular location: Periplasm: P00282
• Total number of polymer chains: 1
• Total formula weight: 14516.86

Authors

Takematsu, K.,Williamson, H.R.,Blanco-Rodriguez, A.M.,Sokolova, L.,Nikolovski, P.,Kaiser, J.T.,Towrie, M.,Clark, I.P.,Vlcek Jr, A.,Winkler, J.R.,Gray, H.B. (deposition date: 2013-04-20, release date: 2013-10-02, Last modification date: 2024-11-06)

Primary citation

Takematsu, K.,Williamson, H.,Blanco-Rodriguez, A.M.,Sokolova, L.,Nikolovski, P.,Kaiser, J.T.,Towrie, M.,Clark, I.P.,Vlcek, A.,Winkler, J.R.,Gray, H.B.
Tryptophan-accelerated electron flow across a protein-protein interface.
J.Am.Chem.Soc., 135:15515-15525, 2013

PubMed Abstract: We report a new metallolabeled blue copper protein, Re126W122Cu(I) Pseudomonas aeruginosa azurin, which has three redox sites at well-defined distances in the protein fold: Re(I)(CO)3(4,7-dimethyl-1,10-phenanthroline) covalently bound at H126, a Cu center, and an indole side chain W122 situated between the Re and Cu sites (Re-W122(indole) = 13.1 Å, dmp-W122(indole) = 10.0 Å, Re-Cu = 25.6 Å). Near-UV excitation of the Re chromophore leads to prompt Cu(I) oxidation (<50 ns), followed by slow back ET to regenerate Cu(I) and ground-state Re(I) with biexponential kinetics, 220 ns and 6 μs. From spectroscopic measurements of kinetics and relative ET yields at different concentrations, it is likely that the photoinduced ET reactions occur in protein dimers, (Re126W122Cu(I))2 and that the forward ET is accelerated by intermolecular electron hopping through the interfacial tryptophan: *Re//←W122←Cu(I), where // denotes a protein-protein interface. Solution mass spectrometry confirms a broad oligomer distribution with prevalent monomers and dimers, and the crystal structure of the Cu(II) form shows two Re126W122Cu(II) molecules oriented such that redox cofactors Re(dmp) and W122-indole on different protein molecules are located at the interface at much shorter intermolecular distances (Re-W122(indole) = 6.9 Å, dmp-W122(indole) = 3.5 Å, and Re-Cu = 14.0 Å) than within single protein folds. Whereas forward ET is accelerated by hopping through W122, BET is retarded by a space jump at the interface that lacks specific interactions or water molecules. These findings on interfacial electron hopping in (Re126W122Cu(I))2 shed new light on optimal redox-unit placements required for functional long-range charge separation in protein complexes.

PubMed: 24032375
DOI: 10.1021/ja406830d

Experimental method

X-RAY DIFFRACTION (1.7 Å)