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Integrative Approaches in Structural Biology: A More Complete Picture from the Combination of Individual Techniques

机译:结构生物学中的整合方法:结合个体技术获得的更完整图片

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摘要

With the recent technological and computational advancements, structural biology has begun to tackle more and more difficult questions, including complex biochemical pathways and transient interactions among macromolecules. This has demonstrated that, to approach the complexity of biology, one single technique is largely insufficient and unable to yield thorough answers, whereas integrated approaches have been more and more adopted with successful results. Traditional structural techniques (X-ray crystallography and Nuclear Magnetic Resonance (NMR)) and the emerging ones (cryo-electron microscopy (cryo-EM), Small Angle X-ray Scattering (SAXS)), together with molecular modeling, have pros and cons which very nicely complement one another. In this review, three examples of synergistic approaches chosen from our previous research will be revisited. The first shows how the joint use of both solution and solid-state NMR (SSNMR), X-ray crystallography, and cryo-EM is crucial to elucidate the structure of polyethylene glycol (PEG)ylated asparaginase, which would not be obtainable through any of the techniques taken alone. The second deals with the integrated use of NMR, X-ray crystallography, and SAXS in order to elucidate the catalytic mechanism of an enzyme that is based on the flexibility of the enzyme itself. The third one shows how it is possible to put together experimental data from X-ray crystallography and NMR restraints in order to refine a protein model in order to obtain a structure which simultaneously satisfies both experimental datasets and is therefore closer to the ‘real structure’.
机译:随着最近技术和计算的进步,结构生物学已开始解决越来越多的难题,包括复杂的生化途径和大分子之间的瞬时相互作用。这表明,要解决生物学的复杂性,单一的技术在很大程度上是不够的,并且无法提供详尽的答案,而集成的方法已被越来越多的采用,并取得了成功的结果。传统的结构技术(X射线晶体学和核磁共振(NMR))和新兴的结构技术(低温电子显微镜(Cryo-EM),小角X射线散射(SAXS))以及分子建模技术都有其优缺点。缺点,可以很好地相互补充。在这篇综述中,将从我们先前的研究中选择的三个协同方法的例子进行回顾。第一个显示了溶液和固态NMR(SSNMR),X射线晶体学和cryo-EM的联合使用对于阐明聚乙二醇(PEG)酰化的天冬酰胺酶的结构至关重要,而这是无法通过任何方法获得的。单独采取的技术。第二部分涉及NMR,X射线晶体学和SAXS的综合使用,以便阐明基于酶本身的柔韧性的酶催化机理。第三个展示了如何将来自X射线晶体学和NMR约束的实验数据汇总在一起,以完善蛋白质模型,从而获得同时满足两个实验数据集并因此更接近“真实结构”的结构。

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