Francis William J C, Grewal Harmanjot, Wainwright Alexander A C, Yang Xuchun, Olivucci Massimo, Miller R J Dwayne
Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada and Department of Physics, University of Toronto, 60 St. George Street, Toronto, Ontario M5S 3J1, Canada.
Struct Dyn. 2024 Mar 1;11(2):024301. doi: 10.1063/4.0000239. eCollection 2024 Mar.
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.
理解产生功能性生物系统的化学反应是结构生物学的核心。随着研究驱动生物过程的化学反应的技术不断发展,必须确保发生的反应确实是一条与生物学相关的途径。越来越多的证据表明,在光活性生物过程的研究中存在系统误差的传播;用于探测光激活蛋白功能结构动力学的光学方法未能确保光激发准备好与感兴趣的生物过程相关的明确初始状态。自然界中的光激发发生在线性(每个发色团一个光子)状态;然而,实验中使用的极端激发条件会导致与生物学无关的多光子吸收。为了评估和确保过去和未来实验的生物学相关性,已经开发了一个理论框架来确定激发条件,该条件会导致共振多光子吸收(RMPA),从而总体上定义了在单光子激发状态下研究结构动力学的激发极限。在这里,我们将理论模型应用于细菌视紫红质(bR),并表明当激发条件超过线性饱和阈值时会发生RMPA,该阈值远低于此类实验中使用的典型激发条件。这项工作提供了指导方针,以确保线性单光子状态下的激发与生物和化学过程相关。