Electron tunneling in rhenium-modified Pseudomonas aeruginosa azurins
Abstract
Laser flash-quench methods have been used to generate tyrosine and tryptophan radicals in structurally characterized rhenium-modified Pseudomonas aeruginosa azurins. Cu(I) to "Re(II)" electron tunneling in Re(H107) azurin occurs in the microsecond range. This reaction is much faster than that studied previously for Cu(I) to Ru(III) tunneling in Ru(H107) azurin, suggesting that a multistep ("hopping") mechanism might be involved. Although a Y108 radical can be generated by flash-quenching a Re(H107)M(II) (M=Cu, Zn) protein, the evidence suggests that it is not an active intermediate in the enhanced Cu(I) oxidation. Rather, the likely explanation is rapid conversion of Re(II)(H107) to deprotonated Re(I)(H107 radical), followed by electron tunneling from Cu(I) to the hole in the imidazole ligand.
Additional Information
© 2004 Elsevier B.V. Received 24 April 2003, Revised 26 June 2003, Accepted 26 June 2003, Available online 7 January 2004. Our research on electron tunneling in proteins is supported by NIH grant DK19038.Attached Files
Published - 1-s2.0-S0005272803002238-main.pdf
Files
Name | Size | Download all |
---|---|---|
md5:5313c5d158b63d8e342d2e0496db092b
|
722.8 kB | Preview Download |
Additional details
- Eprint ID
- 77846
- Resolver ID
- CaltechAUTHORS:20170531-085753394
- NIH
- DK19038
- Created
-
2017-05-31Created from EPrint's datestamp field
- Updated
-
2021-11-15Created from EPrint's last_modified field