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Redox conditions correlated with vibronic coupling modulate quantum beats in photosynthetic pigment–protein complexes

Significance Photosynthetic organisms evolved their light-harvesting antenna complexes to optimize energy transfer. It was recently shown that the redox environment can tune the mixing of electronic and vibrational states to steer energy through different pathways of a pigment–protein complex. Quantum beating signals in the spectra of pigment–protein complexes have been used to probe the excited-state dynamics within the complexes, but the microscopic dynamics that generate these signals and their role in promoting energy transfer are not fully understood. Here, we show that the redox environment that tunes energy transfer similarly tunes the quantum beating signals in the same complex. We find that the beats report on excited-state vibrations that maintain coherence through the vibronically enhanced energy transfer process.
- University of Mary United States
- University of Chicago United States
- Washington State University United States
Light, Pigmentation, Spectrum Analysis, Photosynthetic Reaction Center Complex Proteins, Light-Harvesting Protein Complexes, Vibration, Bacterial Proteins, Energy Transfer, Quantum Theory, Photosynthesis, Oxidation-Reduction
Light, Pigmentation, Spectrum Analysis, Photosynthetic Reaction Center Complex Proteins, Light-Harvesting Protein Complexes, Vibration, Bacterial Proteins, Energy Transfer, Quantum Theory, Photosynthesis, Oxidation-Reduction
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).14 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
