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Primary Reactions of the LOV2 Domain of Phototropin Studied with Ultrafast Mid-Infrared Spectroscopy and Quantum Chemistry

机译:超快中红外光谱和量子化学研究光蛋白的LOV2结构域的主要反应

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摘要

Phototropins, major blue-light receptors in plants, are sensitive to blue light through a pair of flavin mononucleotide (FMN)-binding light oxygen and voltage (LOV) domains, LOV1 and LOV2. LOV2 undergoes a photocycle involving light-driven covalent adduct formation between a conserved cysteine and the FMN C(4a) atom. Here, the primary reactions of Avena sativa phototropin 1 LOV2 (AsLOV2) were studied using ultrafast mid-infrared spectroscopy and quantum chemistry. The singlet excited state (S1) evolves into the triplet state (T1) with a lifetime of 1.5 ns at a yield of ∼50%. The infrared signature of S1 is characterized by absorption bands at 1657 cm−1, 1495–1415 cm−1, and 1375 cm−1. The T1 state shows infrared bands at 1657 cm−1, 1645 cm−1, 1491–1438 cm−1, and 1390 cm−1. For both electronic states, these bands are assigned principally to C=O, C=N, C-C, and C-N stretch modes. The overall downshifting of C=O and C=N bond stretch modes is consistent with an overall bond-order decrease of the conjugated isoalloxazine system upon a π-π∗ transition. The configuration interaction singles (CIS) method was used to calculate the vibrational spectra of the S1 and T1 excited ππ∗ states, as well as respective electronic energies, structural parameters, electronic dipole moments, and intrinsic force constants. The harmonic frequencies of S1 and T1, as calculated by the CIS method, are in satisfactory agreement with the evident band positions and intensities. On the other hand, CIS calculations of a T1 cation that was protonated at the N(5) site did not reproduce the experimental FMN T1 spectrum. We conclude that the FMN T1 state remains nonprotonated on a nanosecond timescale, which rules out an ionic mechanism for covalent adduct formation involving cysteine-N(5) proton transfer on this timescale. Finally, we observed a heterogeneous population of singly and doubly H-bonded FMN C(4)=O conformers in the dark state, with stretch frequencies at 1714 cm−1 and 1694 cm−1, respectively.
机译:光合蛋白是植物中的主要蓝光受体,通过一对结合黄素单核苷酸(FMN)的轻氧和电压(LOV)域LOV1和LOV2对蓝光敏感。 LOV2经历一个光循环,其中涉及在一个保守的半胱氨酸和FMN C(4a)原子之间形成光驱动的共价加合物。在这里,使用超快中红外光谱法和量子化学研究了燕麦燕麦光合蛋白1 LOV2(AsLOV2)的主要反应。单重态激发态(S1)演化为三重态(T1),寿命为1.5 ns,产率约为50%。 S1的红外特征是在1657 cm-1、1495-1415 cm-1和1375 cm-1处有吸收带。 T1状态显示1657 cm-1、1645 cm-1、1491-1438 cm-1和1390 cm-1的红外波段。对于两种电子状态,这些频带主要分配给C = O,C = N,CC-C和C-N拉伸模式。 C = O和C = N键拉伸模式的整体下移与π-π*跃迁时共轭异四恶嗪系统的整体键序降低一致。构型相互作用单(CIS)方法用于计算S1和T1激发的ππ∗态的振动谱,以及各自的电子能量,结构参数,电子偶极矩和固有力常数。通过CIS方法计算出的S1和T1的谐波频率与表观频带位置和强度均令人满意。另一方面,在N(5)位置质子化的T1阳离子的CIS计算没有重现实验FMN T1光谱。我们得出的结论是,FMN T1状态在纳秒级时标上仍未质子化,这排除了在此时标上涉及半胱氨酸-N(5)质子转移的共价加合物形成的离子机制。最后,我们观察到在黑暗状态下单键和双键HMN的FMN C(4)= O构象异构体的异质性,其拉伸频率分别为1714 cm-1和1694 cm-1。

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