Rajagopal Sudarshan, Anderson Spencer, Srajer Vukica, Schmidt Marius, Pahl Reinhard, Moffat Keith
Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637, USA.
Structure. 2005 Jan;13(1):55-63. doi: 10.1016/j.str.2004.10.016.
In the bacterial photoreceptor photoactive yellow protein (PYP), absorption of blue light by its chromophore leads to a conformational change in the protein associated with differential signaling activity, as it executes a reversible photocycle. Time-resolved Laue crystallography allows structural snapshots (as short as 150 ps) of high crystallographic resolution (approximately 1.6 A) to be taken of a protein as it functions. Here, we analyze by singular value decomposition a comprehensive time-resolved crystallographic data set of the E46Q mutant of PYP throughout the photocycle spanning 10 ns-100 ms. We identify and refine the structures of five distinct intermediates and provide a plausible chemical kinetic mechanism for their inter conversion. A clear structural progression is visible in these intermediates, in which a signal generated at the chromophore propagates through a distinct structural pathway of conserved residues and results in structural changes near the N terminus, over 20 A distant from the chromophore.
在细菌光感受器光活性黄色蛋白(PYP)中,其发色团对蓝光的吸收会导致蛋白质发生构象变化,这种变化与不同的信号传导活性相关,因为它会执行一个可逆的光循环。时间分辨劳厄晶体学能够在蛋白质发挥功能时拍摄高晶体分辨率(约1.6埃)的结构快照(短至150皮秒)。在此,我们通过奇异值分解分析了PYP的E46Q突变体在跨越10纳秒至100毫秒的光循环过程中的综合时间分辨晶体学数据集。我们识别并优化了五个不同中间体的结构,并为它们的相互转化提供了一个合理的化学动力学机制。在这些中间体中可以看到明显的结构进展,其中发色团产生的信号通过保守残基的独特结构途径传播,并导致在距发色团超过20埃的N端附近发生结构变化。