4.8 Article

Few-fs resolution of a photoactive protein traversing a conical intersection

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NATURE
卷 599, 期 7886, 页码 697-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-021-04050-9

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资金

  1. US Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0002164]
  2. US National Science Foundation [STC-1231306, DBI-2029533]
  3. Cluster of Excellence 'CUI: Advanced Imaging of Matter' of Deutsche Forschungsgemeinschaft (DFG) [EXC 2056, 390715994]

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This study presents atomic-resolution videos of photoactive yellow protein passing through a conical intersection, extracted from experimental data by machine learning. The videos reveal dynamic trajectories, key parameters, and the topography of electronic potential energy surfaces involved in the de-excitation process.
The structural dynamics of a molecule are determined by the underlying potential energy landscape. Conical intersections are funnels connecting otherwise separate potential energy surfaces. Posited almost a century ago(1), conical intersections remain the subject of intense scientific interest(2-5). In biology, they have a pivotal role in vision, photosynthesis and DNA stability(6). Accurate theoretical methods for examining conical intersections are at present limited to small molecules. Experimental investigations are challenged by the required time resolution and sensitivity. Current structure-dynamical understanding of conical intersections is thus limited to simple molecules with around ten atoms, on timescales of about 100 fs or longer(7). Spectroscopy can achieve better time resolutions(8), but provides indirect structural information. Here we present few-femtosecond, atomic-resolution videos of photoactive yellow protein, a 2,000-atom protein, passing through a conical intersection. These videos, extracted from experimental data by machine learning, reveal the dynamical trajectories of de-excitation via a conical intersection, yield the key parameters of the conical intersection controlling the de-excitation process and elucidate the topography of the electronic potential energy surfaces involved.

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