Skou Magda, Skou Søren, Jensen Thomas G, Vestergaard Bente, Gillilan Richard E
Department of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.
Department of Structural Biophysics, University of Copenhagen, Universitetsparken 6, DK-2100 Copenhagen, Denmark ; MacCHESS (Macromolecular Diffraction Facility at CHESS), Cornell University, Ithaca, NY 14853, USA.
J Appl Crystallogr. 2014 Aug 1;47(Pt 4):1355-1366. doi: 10.1107/S1600576714012618.
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.
由于同步加速器小角X射线(溶液)散射(SAXS)光束线对低样品消耗和自动换样能力的需求,X射线微流体技术受到越来越多的关注。在此,展示了一种遥控微流体装置,用于在蛋白质透析过程中同时进行SAXS和紫外吸收测量,该装置直接集成在SAXS光束线上。微流体透析可用于监测因缓冲液交换或如所示的蛋白质浓度变化而引起的结构变化。通过在浓缩过程中收集X射线数据,消除了因过度浓缩和储存导致蛋白质聚集的风险,从而减少了样品消耗并提高了数据质量。概念验证展示了微流体装置中停止或连续流动的效果。在这些实验所达到的水平下,浓缩过程未诱导样品聚集。对装置内流体动力学和传输特性的模拟强烈表明,聚集体甚至可能更高阶的寡聚体优先被装置保留,从而实现了偶然的样品纯化。因此,这种多功能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。