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首页> 外文期刊>Chemphyschem: A European journal of chemical physics and physical chemistry >Non-Bonded Interactions Drive the Sub-Picosecond Bilin Photoisomerization in the P-fr State of Phytochrome Cph1
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Non-Bonded Interactions Drive the Sub-Picosecond Bilin Photoisomerization in the P-fr State of Phytochrome Cph1

机译:非键相互作用在植物色素Cph1的P-fr状态下驱动亚皮秒级Bilin光异构化。

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摘要

Phytochromes are protein-based photoreceptors harboring a bilin-based photoswitch in the active site. The timescale of photosignaling via C-15=C-16 E-to-Z photoisomerization has been ambiguous in the far-red-absorbing P-fr state. Here we present a unified view of the structural events in phytochrome Cph1 post excitation with femtosecond precision, obtained via stimulated Raman and polarization-resolved transient IR spectroscopy. We demonstrate that photoproduct formation occurs within 700fs, determined by a two-step partitioning process initiated by a planarization on the electronic excited state with a 300fs time scale. The ultrafast isomerization timescale for P-fr-to-P-r conversion highlights the active role of the nonbonding methyl-methyl clash initiating the reaction in the excited state. We envision that our results will motivate the synthesis of new artificial photoswitches with precisely tuned non-bonded interactions for ultrafast response.
机译:植物色素是基于蛋白质的感光体,在活性位点具有基于Bilin的感光开关。通过C-15 = C-16 E-Z光异构化进行光晕的时间尺度在吸收远红光的P-fr状态下是模棱两可的。在这里,我们通过激发拉曼光谱和偏振分辨瞬态红外光谱获得了飞秒精度激发后的植物色素Cph1中结构事件的统一视图。我们证明光产物的形成发生在700fs内,这是由两步分区过程决定的,该过程由在300fs时标上的电子激发态的平面化启动。 P-fr-to-P-r转化的超快异构化时间尺度突出了非键合甲基-甲基碰撞在激发态下引发反应的积极作用。我们设想,我们的结果将激发具有精确调整的非键合相互作用的新型人造光开关的合成,以实现超快响应。

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