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时间分辨连续飞秒晶体学在脂肪酸脱羧酶上的应用:经验教训。

Time-resolved serial femtosecond crystallography on fatty-acid photodecarboxylase: lessons learned.

机构信息

Université Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale, 38000 Grenoble, France.

Max-Planck-Institut für medizinische Forschung, Jahnstrasse 29, 69120 Heidelberg, Germany.

出版信息

Acta Crystallogr D Struct Biol. 2022 Sep 1;78(Pt 9):1131-1142. doi: 10.1107/S2059798322007525. Epub 2022 Aug 25.

Abstract

Upon absorption of a blue-light photon, fatty-acid photodecarboxylase catalyzes the decarboxylation of free fatty acids to form hydrocarbons (for example alkanes or alkenes). The major components of the catalytic mechanism have recently been elucidated by combining static and time-resolved serial femtosecond crystallography (TR-SFX), time-resolved vibrational and electronic spectroscopies, quantum-chemical calculations and site-directed mutagenesis [Sorigué et al. (2021), Science, 372, eabd5687]. The TR-SFX experiments, which were carried out at four different picosecond to microsecond pump-probe delays, yielded input for the calculation of Fourier difference maps that demonstrated light-induced decarboxylation. Here, some of the difficulties encountered during the experiment as well as during data processing are highlighted, in particular regarding space-group assignment, a pump-laser power titration is described and data analysis is extended by structure-factor extrapolation of the TR-SFX data. Structure refinement against extrapolated structure factors reveals a reorientation of the generated hydrocarbon and the formation of a photoproduct close to Cys432 and Arg451. Identification of its chemical nature, CO or bicarbonate, was not possible because of the limited data quality, which was assigned to specificities of the crystalline system. Further TR-SFX experiments on a different crystal form are required to identify the photoproducts and their movements during the catalytic cycle.

摘要

在吸收一个蓝光光子后,脂肪酸光脱羧酶催化游离脂肪酸的脱羧反应,形成烃类(例如烷烃或烯烃)。最近,通过结合静态和时间分辨连续飞秒晶体学(TR-SFX)、时间分辨振动和电子光谱学、量子化学计算和定点突变[ Sorigué 等人(2021),《科学》,372,eabd5687],阐明了该催化机制的主要组成部分。在四个不同的皮秒到微秒的泵浦探测延迟时间进行的 TR-SFX 实验,为计算傅里叶差分图提供了输入,该图证明了光诱导的脱羧反应。在这里,突出了实验过程中和数据处理过程中遇到的一些困难,特别是关于空间群的分配,描述了一个泵浦激光功率滴定,并通过 TR-SFX 数据的结构因子外推扩展了数据分析。对外推结构因子的结构精修揭示了生成的烃的重定向以及靠近 Cys432 和 Arg451 的光产物的形成。由于数据质量有限,无法确定其化学性质是 CO 还是碳酸氢盐,这归因于结晶体系的特异性。需要进行进一步的 TR-SFX 实验,以确定不同晶型的光产物及其在催化循环中的运动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de0a/9435596/15a8a35a9e3a/d-78-01131-fig1.jpg

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