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Size-exclusion chromatography small-angle X-ray scattering of water soluble proteins on a laboratory instrument

机译:尺寸排阻色谱法在实验室仪器上对水溶性蛋白质进行小角度X射线散射

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摘要

Coupling of size-exclusion chromatography with biological solution small-angle X-ray scattering (SEC-SAXS) on dedicated synchrotron beamlines enables structural analysis of challenging samples such as labile proteins and low-affinity complexes. For this reason, the approach has gained increased popularity during the past decade. Transportation of perishable samples to synchrotrons might, however, compromise the experiments, and the limited availability of synchrotron beamtime renders iterative sample optimization tedious and lengthy. Here, the successful setup of laboratory-based SEC-SAXS is described in a proof-of-concept study. It is demonstrated that sufficient quality data can be obtained on a laboratory instrument with small sample consumption, comparable to typical synchrotron SEC-SAXS demands. UV/vis measurements directly on the SAXS exposure cell ensure accurate concentration determination, crucial for direct molecular weight determination from the scattering data. The absence of radiation damage implies that the sample can be fractionated and subjected to complementary analysis available at the home institution after SEC-SAXS. Laboratory-based SEC-SAXS opens the field for analysis of biological samples at the home institution, thus increasing productivity of biostructural research. It may further ensure that synchrotron beamtime is used primarily for the most suitable and optimized samples.
机译:体积排阻色谱与生物溶液小角X射线散射(SEC-SAXS)在专用同步加速器射线线上的耦合可对具有挑战性的样品(如不稳定的蛋白质和低亲和力的复合物)进行结构分析。因此,在过去的十年中,这种方法越来越受欢迎。然而,易腐烂样品向同步加速器的运输可能会损害实验,并且同步加速器束流时间的有限可用性使迭代样品优化变得繁琐而冗长。在这里,概念验证研究描述了基于实验室的SEC-SAXS的成功设置。结果表明,与典型的同步加速器SEC-SAXS要求相比,可以在实验室仪器上以较少的样品消耗获得足够的质量数据。直接在SAXS曝光池上进行的UV / vis测量可确保准确的浓度测定,这对于从散射数据直接测定分子量至关重要。没有辐射损伤意味着SEC-SAXS之后可以对样品进行分级分离,并进行家庭机构的补充分析。基于实验室的SEC-SAXS为家庭机构中的生物样品分析开辟了领域,从而提高了生物结构研究的生产率。可以进一步确保同步加速器波束时间主要用于最合适和最优化的样本。

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