Light-Induced Nanosecond Relaxation Dynamics of Rhenium-Labeled Pseudomonas aeruginosa Azurins

0522287 - ÚFCH JH 2021 RIV US eng J - Journal Article
Pospíšil, Petr - Sýkora, Jan - Takematsu, K. - Hof, Martin - Gray, H. B. - Vlček, Antonín
Light-Induced Nanosecond Relaxation Dynamics of Rhenium-Labeled Pseudomonas aeruginosa Azurins.
Journal of Physical Chemistry B. Roč. 124, č. 5 (2020), s. 788-797. ISSN 1520-6106. E-ISSN 1520-5207
R&D Projects: GA ČR GA17-01137S; GA MŠMT(CZ) LTAUSA18026
Institutional support: RVO:61388955
Keywords : EXCITED-STATE DYNAMICS * ACCELERATED ELECTRON FLOW * SOLVATION DYNAMICS
OECD category: Physical chemistry
Impact factor: 2.991, year: 2020
Method of publishing: Limited access

Time-resolved phosphorescence spectra of Re(CO)3(dmp)+ and Re(CO)3(phen)+ chromophores (dmp = 4,7-dimethyl-1,10-phenanthroline, phen = 1,10-phenanthroline) bound to surface histidines (H83, H124, and H126) of Pseudomonas aeruginosa azurin mutants exhibit dynamic band maxima shifts to lower wavenumbers following 3-exponential kinetics with 1-5 and 20-100 ns major phases and a 1.1-2.5 μs minor (5-16%) phase. Observation of slow relaxation components was made possible by using an organometallic Re chromophore as a probe whose long phosphorescence lifetime extends the observation window up to ∼3 μs. Integrated emission-band areas also decay with 2- or 3-exponential kinetics. The faster decay phase(s) is relaxation-related, whereas the slowest one [360-680 ns (dmp), 90-140 ns (phen)] arises mainly from population decay. As a result of shifting bands, the emission intensity decay kinetics depend on the detection wavelength. Detailed kinetics analyses and comparisons with band-shift dynamics are needed to disentangle relaxation and population decay kinetics if they occur on comparable timescales. The dynamic phosphorescence Stokes shift in Re-azurins is caused by relaxation motions of the solvent, the protein, and solvated amino acid side chains at the Re binding site in response to chromophore electronic excitation. Comparing relaxation and decay kinetics of Re(dmp)124K122CuII and Re(dmp)124W122CuII suggests that electron transfer (ET) and relaxation motions in the W122 mutant are coupled. It follows that nanosecond and faster photo-induced ET steps in azurins (and likely other redox proteins) occur from unrelaxed systems, importantly, these reactions can be driven (or hindered) by structural and solvational dynamics.
Permanent Link: http://hdl.handle.net/11104/0306802