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Atom-scale depth localization of biologically important chemical elements in molecular layers

机译:分子层中生物重要化学元素的原子尺度深度定位

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摘要

In nature, biomolecules are often organized as functional thin layers in interfacial architectures, the most prominent examples being biological membranes. Biomolecular layers play also important roles in context with biotechnological surfaces, for instance, when they are the result of adsorption processes. For the understanding of many biological or biotechnologically relevant phenomena, detailed structural insight into the involved biomolecular layers is required. Here, we use standing-wave X-ray fluorescence (SWXF) to localize chemical elements in solid-supported lipid and protein layers with near-Ångstrom precision. The technique complements traditional specular reflectometry experiments that merely yield the layers’ global density profiles. While earlier work mostly focused on relatively heavy elements, typically metal ions, we show that it is also possible to determine the position of the comparatively light elements S and P, which are found in the most abundant classes of biomolecules and are therefore particularly important. With that, we overcome the need of artificial heavy atom labels, the main obstacle to a broader application of high-resolution SWXF in the fields of biology and soft matter. This work may thus constitute the basis for the label-free, element-specific structural investigation of complex biomolecular layers and biological surfaces.
机译:在自然界中,生物分子通常在界面结构中被组织成功能薄层,最突出的例子是生物膜。生物分子层在生物技术表面中也起着重要作用,例如当它们是吸附过程的结果时。为了理解许多生物学或生物技术上相关的现象,需要对涉及的生物分子层进行详细的结构分析。在这里,我们使用驻波X射线荧光(SWXF)将化学元素定位在固体支持的脂质和蛋白质层中,精确度接近埃。该技术是对传统镜面反射测量法实验的补充,后者仅能得出各层的整体密度分布。虽然较早的工作主要集中在相对较重的元素(通常是金属离子)上,但我们表明,还可以确定相对较轻的元素S和P的位置,这些元素在最丰富的生物分子类别中发现,因此特别重要。这样,我们就克服了人工重原子标记的需要,而后者是高分辨率SWXF在生物学和软物质领域更广泛应用的主要障碍。因此,这项工作可能构成了对复杂生物分子层和生物表面进行无标记,元素特定的结构研究的基础。

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