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Structure and dynamics of biomacromolecules in solution: recent developments and future perspectives in SANS/SAXS and neutron spectroscopy

机译:溶液中生物大分子的结构和动力学:SANS / SAXS和中子光谱学的最新发展和未来展望

摘要

This French University Habilitation (“mémoire” to obtain the “Diplôme d’Habilitation à Diriger des Recherches”, DHDR) is divided into two parts: the first one deals with the results that I have obtained after my PhD thesis in 2003, the second one discusses open questions related to theseresults as well as mid- and long-term perspectives.Three different topics are presented in the result chapters: 1) a combination of small angle scattering (SAS) and nuclear magnetic resonance (NMR) for rigid-body modeling of biomacromolecular complexes, 2) the combined use of small angle X-ray (SAXS) and neutron (SANS) scattering for the study of unfolded proteins and 3) the study of biomacromolecular and solvent dynamics by neutron spectroscopy combining several instruments.Points 1) and 3) are discussed in great detail, both in the results and perspective sections, since they represent the most advanced projects of my research. Point 2) is dealt with more briefly in the results section, since few results are available so far. However, perspectives are discussed. Aspecial perspective chapter deals with applications on membrane proteins. Key publications for the different chapters are:Chapter 1: Gabel et al. (2006) A target function for quaternary structural refinement from small angle scattering and NMR orientational restraints. Eur. Biophys. J. 35(4), 313-327. Gabel et al. (2008) A structure refinement protocol combining NMR residual dipolar couplings and small angle scattering restraints. J. Biomol. NMR 41(4), 199-208.Chapter 2: Gabel et al. (2009) Quantitative Modelfree Analysis of Urea Binding to Unfolded Ubiquitin Using a Combination of Small Angle X-ray and Neutron Scattering. J. Am. Chem. Soc. 131(25), 8769-8771.Chapter 3: Gabel (2005) Protein dynamics in solution and powder measured by incoherent elastic neutron scattering: the influence of Q-range and energy resolution. Eur. Biophys. J. 31(1), 1-12. Gabel & Bellissent-Funel (2007) C-Phycocyanin Hydration Water Dynamics in the Presence of Trehalose: An Incoherent Elastic Neutron Scattering Study at Different Energy Resolutions. Biophys. J. 92(11), 4054-4063.The habilitation thesis is focused on methodological aspects and developments of small angle scattering and neutron spectroscopy. It is obvious that the approaches discussed here and their sophisticated levels of data analysis rely fundamentally on the quality of the sample, and inparticular on monodispersity (for SAS) and amount of material for spectroscopy. The paramount importance of good biochemistry and the use of complementary techniques for the characterization of samples can hardly be overestimated. They include, amongst others, gelfiltration, analytical ultracentrifugation, static and dynamic light scattering, NMR, etc. They are quite simply indispensable for doing good and accurate science with SAS, in particular in more complex systems (macromolecular complexes, membrane proteins …). If they are not presentedin more detail in this thesis, it is not out of ignorance of this fact but due to the lack of space.
机译:这项法国大学的适应训练课程(“Mémoire”,即获得“Dipliômed'HabilitationàDiriger des Recherches”,DHDR)分为两部分:第一部分涉及我在2003年获得博士学位后获得的结果,第二部分涉及结果章节中提出了三个不同的主题:1)小角度散射(SAS)和核磁共振(NMR)结合用于刚体生物大分子复合物的建模,2)小角度X射线(SAXS)和中子(SANS)散射的结合用于研究未折叠的蛋白质和3)中子光谱学结合多种仪器研究生物大分子和溶剂动力学的要点1 )和3)在结果和透视图部分进行了详细讨论,因为它们代表了我研究中最先进的项目。由于到目前为止,几乎没有可用的结果,因此在结果部分中将更简单地处理第2点)。但是,讨论了观点。特殊视角一章涉及膜蛋白的应用。不同章节的主要出版物为:第1章:Gabel等。 (2006)从小角度散射和NMR定向约束进行四级结构优化的目标函数。欧元。生物物理学。 J.35(4),313-327。 Gabel等。 (2008)结合NMR残留偶极耦合和小角度散射约束的结构细化方案。 J.生物分子。 NMR 41(4),199-208。第二章:Gabel等。 (2009)使用小角度X射线和中子散射相结合的尿素与未折叠的泛素结合的无模型定量分析。 J.上午化学Soc。 131(25),8769-8771。第3章:Gabel(2005)通过非相干弹性中子散射测量溶液和粉末中的蛋白质动力学:Q范围和能量分辨率的影响。欧元。生物物理学。 J.31(1),1-12。 Gabel&Bellissent-Funel(2007)海藻糖存在下的C-藻蓝蛋白水合水动力学:不同能量分辨率下的非相干弹性中子散射研究。生物物理学。 J. 92(11),4054-4063。适应性论文的重点是小角度散射和中子光谱学的方法论方面和发展。显然,这里讨论的方法及其复杂的数据分析水平从根本上取决于样品的质量,尤其是取决于单分散性(对于SAS)和光谱学材料的数量。良好的生物化学的最高重要性以及使用互补技术表征样品的能力几乎不能被高估。它们包括凝胶过滤,分析超速离心,静态和动态光散射,NMR等。对于使用SAS进行良好而精确的科学,尤其是在更复杂的系统(大分子复合物,膜蛋白等)中,它们是必不可少的。如果在本文中未对它们进行更详细的介绍,则不是因为没有事实,而是由于缺乏空间。

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    Gabel Frank;

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