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A microfabricated fixed path length silicon sample holder improves background subtraction for cryoSAXS

机译:微型固定路径长度的硅样品架改善了cryoSAXS的背景扣除

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摘要

The application of small-angle X-ray scattering (SAXS) for high-throughput characterization of biological macromolecules in solution is limited by radiation damage. By cryocooling samples, radiation damage and required sample volumes can be reduced by orders of magnitude. However, the challenges of reproducibly creating the identically sized vitrified samples necessary for conventional background subtraction limit the widespread adoption of this method. Fixed path length silicon sample holders for cryoSAXS have been microfabricated to address these challenges. They have low background scattering and X-ray absorption, require only 640 nl of sample, and allow reproducible sample cooling. Data collected in the sample holders from a nominal illuminated sample volume of 2.5 nl are reproducible down to q ≃ 0.02 Å−1, agree with previous cryoSAXS work and are of sufficient quality for reconstructions that match measured crystal structures. These sample holders thus allow faster, more routine cryoSAXS data collection. Additional development is required to reduce sample fracturing and improve data quality at low q.
机译:小角X射线散射(SAXS)在溶液中生物大分子高通量表征中的应用受到辐射损伤的限制。通过低温冷却样品,可以将辐射损伤和所需样品量减少几个数量级。但是,可重复创建常规背景减法所需的大小相同的玻璃化样品的挑战限制了该方法的广泛采用。为了应对这些挑战,已经对用于cryoSAXS的固定路径长度的硅样品架进行了微加工。它们具有较低的背景散射和X射线吸收,仅需要640µnl的样品,并允许可重现的样品冷却。从标称照明样品体积为2.5 nl的样品架中收集的数据可重现至q≃0.02Å -1 ,与以前的cryoSAXS工作一致,并且具有足够的质量来进行与测得的晶体结构匹配的重建。因此,这些样品架可以更快,更常规地收集cryoSAXS数据。需要进一步开发以减少样品破裂并提高低q值的数据质量。

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