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In situ microfluidic dialysis for biological small-angle X-ray scattering

机译:原位微流透析用于生物小角X射线散射

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摘要

Owing to the demand for low sample consumption and automated sample changing capabilities at synchrotron small-angle X-ray (solution) scattering (SAXS) beamlines, X-ray microfluidics is receiving continuously increasing attention. Here, a remote-controlled microfluidic device is presented for simultaneous SAXS and ultraviolet absorption measurements during protein dialysis, integrated directly on a SAXS beamline. Microfluidic dialysis can be used for monitoring structural changes in response to buffer exchange or, as demonstrated, protein concentration. By collecting X-ray data during the concentration procedure, the risk of inducing protein aggregation due to excessive concentration and storage is eliminated, resulting in reduced sample consumption and improved data quality. The proof of concept demonstrates the effect of halted or continuous flow in the microfluidic device. No sample aggregation was induced by the concentration process at the levels achieved in these experiments. Simulations of fluid dynamics and transport properties within the device strongly suggest that aggregates, and possibly even higher-order oligomers, are preferentially retained by the device, resulting in incidental sample purification. Hence, this versatile microfluidic device enables investigation of experimentally induced structural changes under dynamically controllable sample conditions.
机译:由于对同步加速器小角度X射线(溶液)散射(SAXS)光束线的样品消耗量低和具有自动更改样品功能的需求,X射线微流体技术受到越来越多的关注。在这里,提出了一种远程控制的微流控设备,用于在蛋白质透析期间同时进行SAXS和紫外线吸收测量,并直接集成在SAXS束线上。微流透析可用于监测响应缓冲液交换或蛋白浓度变化的结构变化。通过在浓缩过程中收集X射线数据,消除了由于过度浓缩和储存而引起蛋白质聚集的风险,从而减少了样品消耗并提高了数据质量。概念证明证明了微流体装置中停止或连续流动的影响。在这些实验中达到的浓度下,浓缩过程不会引起样品聚集。设备内流体动力学和传输特性的模拟强烈表明,设备会优先保留聚集体,甚至可能是更高阶的低聚物,从而导致偶然的样品纯化。因此,这种通用的微流体装置能够在动态可控的样品条件下研究实验诱导的结构变化。

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