Electron Tunneling through Pseudomonas aeruginosa Azurins on SAM Gold Electrodes
Abstract
Robust voltammetric responses were obtained for wild-type and Y72F/H83Q/Q107H/Y108F azurins adsorbed on CH_3(CH_2)_nSH:HO(CH_2)_mSH (n=m=4,6,8,11; n=13,15 m=11) self-assembled monolayer (SAM) gold electrodes in acidic solution (pH 4.6) at high ionic strengths. Electron-transfer (ET) rates do not vary substantially with ionic strength, suggesting that the SAM methyl headgroup binds to azurin by hydrophobic interactions. The voltammetric responses for both proteins at higher pH values (>4.6 to 11) also were strong. A binding model in which the SAM hydroxyl headgroup interacts with the Asn47 carboxamide accounts for the relatively strong coupling to the copper center that can be inferred from the ET rates. Of particular interest is the finding that rate constants for electron tunneling through n = 8, 13 SAMs are higher at pH 11 than those at pH 4.6, possibly owing to enhanced coupling of the SAM to Asn 47 caused by deprotonation of nearby surface residues.
Additional Information
© 2007 Elsevier. Received 1 August 2007; accepted 18 August 2007; Available online 30 August 2007. Dedicated to Edward Solomon in appreciation of his pioneering work on blue copper proteins. This work was supported by NIH DK19038.Attached Files
Accepted Version - nihms-43140.pdf
Supplemental Material - 1-s2.0-S0020169307005087-fx2.jpg
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Additional details
- PMCID
- PMC2390814
- Eprint ID
- 56973
- Resolver ID
- CaltechAUTHORS:20150424-150000195
- NIH
- DK19038
- Created
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2015-04-24Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field