期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 110, 期 36, 页码 14658-14663出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1314242110
关键词
spectroscopy; reduction potential; energy transduction pathway
资金
- National Science Foundation [CHE-0948211, CHE-1058959]
- National Institutes of Health [DK-31450]
- Postdoctoral Research Abroad Program
- National Science Council, Taiwan (Republic of China)
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0948211, 1058959] Funding Source: National Science Foundation
Within Cu-containing electron transfer active sites, the role of the axial ligand in type 1 sites is well defined, yet its role in the binuclear mixed-valent Cu-A sites is less clear. Recently, the mutation of the axial Met to Leu in a Cu-A site engineered into azurin (Cu-A Az) was found to have a limited effect on E-0 relative to this mutation in blue copper (BC). Detailed low-temperature absorption and magnetic circular dichroism, resonance Raman, and electron paramagnetic resonance studies on Cu-A Az (WT) and its M123X (X = Q, L, H) axial ligand variants indicated stronger axial ligation in M123L/H. Spectroscopically validated density functional theory calculations show that the smaller Delta E-0 is attributed to H2O coordination to the Cu center in the M123L mutant in Cu-A but not in the equivalent BC variant. The comparable stabilization energy of the oxidized over the reduced state in Cu-A and BC (Cu-A similar to 180 mV; BC similar to 250 mV) indicates that the S(Met) influences E-0 similarly in both. Electron delocalization over two Cu centers in Cu-A was found to minimize the Jahn-Teller distortion induced by the axial Met ligand and lower the inner-sphere reorganization energy. The Cu-S(Met) bond in oxidized Cu-A is weak (5.2 kcal/mol) but energetically similar to that of BC, which demonstrates that the protein matrix also serves an entatic role in keeping the Met bound to the active site to tune down E-0 while maintaining a low reorganization energy required for rapid electron transfer under physiological conditions.
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