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Terahertz radiation induces non-thermal structural changes associated with Fr?hlich condensation in a protein crystal

机译:太赫兹辐射诱导与蛋白质晶体中Fr?hlich缩合有关的非热结构变化

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Whether long-range quantum coherent states could exist in biological systems, and beyond low-temperature regimes where quantum physics is known to be applicable, has been the subject to debate for decades. It was proposed by Fr?hlich that vibrational modes within protein molecules can order and condense into a lowest-frequency vibrational mode in a process similar to Bose-Einstein condensation, and thus that macroscopic coherence could potentially be observed in biological systems. Despite the prediction of these so-called Fr?hlich condensates almost five decades ago, experimental evidence thereof has been lacking. Here, we present the first experimental observation of Fr?hlich condensation in a protein structure. To that end, and to overcome the challenges associated with probing low-frequency molecular vibrations in proteins (which has hampered understanding of their role in proteins' function), we combined terahertz techniques with a highly sensitive X-ray crystallographic method to visualize low-frequency vibrational modes in the protein structure of hen-egg white lysozyme. We found that 0.4 THz electromagnetic radiation induces non-thermal changes in electron density. In particular, we observed a local increase of electron density in a long α-helix motif consistent with a subtle longitudinal compression of the helix. These observed electron density changes occur at a low absorption rate indicating that thermalization of terahertz photons happens on a micro- to milli-second time scale, which is much slower than the expected nanosecond time scale due to damping of delocalized low frequency vibrations. Our analyses show that the micro- to milli-second lifetime of the vibration can only be explained by Fr?hlich condensation, a phenomenon predicted almost half a century ago, yet never experimentally confirmed.
机译:数十年来,是否存在长距离量子相干态存在于生物系统中以及超出已知量子物理学适用的低温范围之外的问题。 Fr?hlich提出,蛋白质分子内的振动模式可以在类似于Bose-Einstein凝聚的过程中有序并凝结为最低频率的振动模式,因此可以在生物系统中观察到宏观相干性。尽管在大约五十年前就预测了这些所谓的Fr?hlich冷凝物,但仍缺乏实验证据。在这里,我们提出蛋白质结构中Frhlich缩合的第一个实验观察。为此,为了克服与探测蛋白质中的低频分子振动相关的挑战(这阻碍了对其在蛋白质功能中的作用的理解),我们将太赫兹技术与高灵敏度的X射线晶体学方法结合使用,以可视化低蛋白色溶菌酶的蛋白质结构中的频率振动模式。我们发现0.4 THz电磁辐射会引起电子密度的非热变化。特别是,我们观察到长的α-螺旋基序中电子密度的局部增加,这与螺旋线的细微纵向压缩相一致。这些观察到的电子密度变化以低吸收率发生,这表明太赫兹光子的热化发生在微秒至毫秒级的时间尺度上,这比预期的纳秒级的时间尺度要慢得多,这归因于离域低频振动的衰减。我们的分析表明,振动的微秒至毫秒的寿命只能用Fr?hlich凝结来解释,Fr?hlich凝结是在半个世纪前就预测到的现象,但从未得到实验证实。

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