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通过计量光束线的同步加速器X射线足迹法研究生物大分子溶液状态结构的SOLEIL项目。

SOLEIL shining on the solution-state structure of biomacromolecules by synchrotron X-ray footprinting at the Metrology beamline.

作者信息

Baud A, Aymé L, Gonnet F, Salard I, Gohon Y, Jolivet P, Brodolin K, Da Silva P, Giuliani A, Sclavi B, Chardot T, Mercère P, Roblin P, Daniel R

机构信息

CNRS, UMR8587, Laboratoire Analyse et Modélisation pour la Biologie et l'Environnement, 91025 Evry, France.

INRA, AgroParisTech, UMR1318, Institut Jean-Pierre Bourgin, 78000 Versailles, France.

出版信息

J Synchrotron Radiat. 2017 May 1;24(Pt 3):576-585. doi: 10.1107/S1600577517002478. Epub 2017 Mar 24.

DOI:10.1107/S1600577517002478
PMID:28452748
Abstract

Synchrotron X-ray footprinting complements the techniques commonly used to define the structure of molecules such as crystallography, small-angle X-ray scattering and nuclear magnetic resonance. It is remarkably useful in probing the structure and interactions of proteins with lipids, nucleic acids or with other proteins in solution, often better reflecting the in vivo state dynamics. To date, most X-ray footprinting studies have been carried out at the National Synchrotron Light Source, USA, and at the European Synchrotron Radiation Facility in Grenoble, France. This work presents X-ray footprinting of biomolecules performed for the first time at the X-ray Metrology beamline at the SOLEIL synchrotron radiation source. The installation at this beamline of a stopped-flow apparatus for sample delivery, an irradiation capillary and an automatic sample collector enabled the X-ray footprinting study of the structure of the soluble protein factor H (FH) from the human complement system as well as of the lipid-associated hydrophobic protein S3 oleosin from plant seed. Mass spectrometry analysis showed that the structural integrity of both proteins was not affected by the short exposition to the oxygen radicals produced during the irradiation. Irradiated molecules were subsequently analysed using high-resolution mass spectrometry to identify and locate oxidized amino acids. Moreover, the analyses of FH in its free state and in complex with complement C3b protein have allowed us to create a map of reactive solvent-exposed residues on the surface of FH and to observe the changes in oxidation of FH residues upon C3b binding. Studies of the solvent accessibility of the S3 oleosin show that X-ray footprinting offers also a unique approach to studying the structure of proteins embedded within membranes or lipid bodies. All the biomolecular applications reported herein demonstrate that the Metrology beamline at SOLEIL can be successfully used for synchrotron X-ray footprinting of biomolecules.

摘要

同步加速器X射线足迹分析补充了常用于确定分子结构的技术,如晶体学、小角X射线散射和核磁共振。它在探测蛋白质与脂质、核酸或溶液中其他蛋白质的结构和相互作用方面非常有用,通常能更好地反映体内状态动态。迄今为止,大多数X射线足迹分析研究都是在美国国家同步加速器光源和法国格勒诺布尔的欧洲同步辐射设施中进行的。这项工作展示了首次在SOLEIL同步辐射源的X射线计量光束线上进行的生物分子X射线足迹分析。在该光束线上安装了用于样品输送的停流装置、辐照毛细管和自动样品收集器,使得能够对人补体系统中的可溶性蛋白因子H(FH)以及植物种子中与脂质相关的疏水蛋白S3油质蛋白的结构进行X射线足迹分析研究。质谱分析表明,两种蛋白质的结构完整性均未受到辐照过程中产生的氧自由基短时间暴露的影响。随后使用高分辨率质谱对辐照后的分子进行分析,以鉴定和定位氧化的氨基酸。此外,对游离状态以及与补体C3b蛋白形成复合物的FH的分析,使我们能够绘制出FH表面反应性溶剂暴露残基的图谱,并观察到C3b结合后FH残基氧化的变化。对S3油质蛋白溶剂可及性的研究表明,X射线足迹分析也为研究嵌入膜或脂质体中的蛋白质结构提供了一种独特的方法。本文报道的所有生物分子应用均表明,SOLEIL的计量光束线可成功用于生物分子的同步加速器X射线足迹分析。

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