Resonant multiphoton processes and excitation limits to structural dynamics

William J. C. Francis, Harmanjot Grewal, Alexander A. C. Wainwright, Xuchun Yang, Massimo Olivucci, R. J. Dwayne Miller
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Abstract

Understanding the chemical reactions that give rise to functional biological systems is at the core of structural biology. As techniques are developed to study the chemical reactions that drive biological processes, it must be ensured that the reaction occurring is indeed a biologically relevant pathway. There is mounting evidence indicating that there has been a propagation of systematic error in the study of photoactive biological processes; the optical methods used to probe the structural dynamics of light activated protein functions have failed to ensure that the photoexcitation prepares a well-defined initial state relevant to the biological process of interest. Photoexcitation in nature occurs in the linear (one-photon per chromophore) regime; however, the extreme excitation conditions used experimentally give rise to biologically irrelevant multiphoton absorption. To evaluate and ensure the biological relevance of past and future experiments, a theoretical framework has been developed to determine the excitation conditions, which lead to resonant multiphoton absorption (RMPA) and thus define the excitation limit in general for the study of structural dynamics within the 1-photon excitation regime. Here, we apply the theoretical model to bacteriorhodopsin (bR) and show that RMPA occurs when excitation conditions exceed the linear saturation threshold, well below typical excitation conditions used in this class of experiments. This work provides the guidelines to ensure excitation in the linear 1-photon regime is relevant to biological and chemical processes.
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共振多光子过程和结构动力学的激发极限
了解产生生物功能系统的化学反应是结构生物学的核心。在开发研究驱动生物过程的化学反应的技术时,必须确保发生的反应确实是与生物相关的途径。越来越多的证据表明,在光活性生物过程的研究中存在着系统误差的传播;用于探测光激活蛋白质功能的结构动态的光学方法未能确保光激发准备了与相关生物过程有关的定义明确的初始状态。自然界中的光激发是线性的(每个发色团一个光子);然而,实验中使用的极端激发条件会产生与生物学无关的多光子吸收。为了评估并确保过去和未来实验的生物相关性,我们开发了一个理论框架来确定激发条件,从而导致共振多光子吸收(RMPA),并由此定义了在单光子激发机制下研究结构动力学的一般激发极限。在此,我们将该理论模型应用于细菌尾视素(bR),结果表明,当激发条件超过线性饱和阈值时,就会发生共振多光子吸收(RMPA),远低于此类实验中使用的典型激发条件。这项工作为确保线性 1 光子激发机制与生物和化学过程相关提供了指导。
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