Long-Range Electron Transfer in Ruthenium-Labelled Myoglobin

• Main Author: Karas, Jennifer Lynn
• Format: Others
• Language: en
• Published: 1989
• Online Access: https://thesis.library.caltech.edu/2520/3/karas-jl_1989.pdf; Karas, Jennifer Lynn (1989) Long-Range Electron Transfer in Ruthenium-Labelled Myoglobin. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/pc6d-xe62. https://resolver.caltech.edu/CaltechETD:etd-06082007-092426 <https://resolver.caltech.edu/CaltechETD:etd-06082007-092426>

<p>The driving force dependence of electron-transfer (ET) reactions has been investigated in protein derivatives of the type <i>trans</i>-Ru(NH₃)₄L-myoglobin (L=NH₃, pyridine, isonicotinamide). In these species, the labelling sites of the ruthenium moiety were determined by proton NMR spectroscopy. ET rates have been measured from the iron(II)-heme in myoglobin to both a₅Ru (a=NH₃) and a₄pyRu (py=pyridine) acceptors bound to histidine 48 (k_ET=0.04 and 2.5 s⁻¹; ΔE°=0.02 and 0.275, respectively). These kinetic results demonstrate for the ruthenium-labelled Mb system that long-range ET is reversible and that the dependence of the ET rates on reaction free energy closely follows Marcus theory. ET rates were also determined for high driving-force systems that were prepared by substitution of palladium and zinc(mesoporphyrin IX), (PdP, ZnP) into the a₄LRu(His-48) derivatives of Mb. ET from the excited state MbMP* (M=Pd or Zn) to the ruthenium acceptor was measured by transient spectroscopy. Reverse ET rates from the surface Ru^II to the ZnP radical cation, (Ru^II→ZnP⁺) were also determined. The ET rates range from 0.04 s⁻¹ for Fe^II→Ru^III ET in a₅Ru(His-48)MbFe (ΔE°=0.02 V), to 3x10⁵ s⁻¹ for ZnP*→Ru^III in a₄isnRu(His48)MbZn (ΔE°=1.2 V). The driving force dependence of the ET rates in the ruthenium-labelled Fe, Zn and Pd(His-48)Mb derivatives has provided information on the reorganization energy. Using Marcus theory, a reorganization energy of 1.5(2) eV has been estimated.</p>