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The Synergetic Effects of Combining Structural Biology and EPR Spectroscopy on Membrane Proteins

机译:结构生物学和EPR光谱相结合对膜蛋白的协同作用

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Protein structures as provided by structural biology such as X-ray crystallography, cryo-electron microscopy and NMR spectroscopy are key elements to understand the function of a protein on the molecular level. Nonetheless, they might be error-prone due to crystallization artifacts or, in particular in case of membrane-imbedded proteins, a mostly artificial environment. In this review, we will introduce different EPR spectroscopy methods as powerful tools to complement and validate structural data gaining insights in the dynamics of proteins and protein complexes such that functional cycles can be derived. We will highlight the use of EPR spectroscopy on membrane-embedded proteins and protein complexes ranging from receptors to secondary active transporters as structural information is still limited in this field and the lipid environment is a particular challenge.
机译:结构生物学(例如X射线晶体学,低温电子显微镜和NMR光谱学)提供的蛋白质结构是了解蛋白质在分子水平上的功能的关键要素。尽管如此,由于结晶伪影或特别是在膜嵌入蛋白的情况下,由于人工晶体的存在,它们可能容易出错。在这篇综述中,我们将介绍不同的EPR光谱方法,作为补充和验证结构数据的强大工具,从而获得有关蛋白质和蛋白质复合物动力学的深刻见解,从而可以得出功能循环。我们将着重介绍EPR光谱技术在膜嵌入的蛋白质和蛋白质复合物(从受体到次级活性转运蛋白)上的应用,因为该领域的结构信息仍然有限,脂质环境是一个特殊的挑战。

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