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PLoS One. 2013 Sep 30;8(9):e74783. doi: 10.1371/journal.pone.0074783. eCollection 2013.
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Publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution.溶液中生物分子小角散射数据结构建模的发表指南。
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Urea separation in flat-plate microchannel hemodialyzer; experiment and modeling.平板式微通道血液透析器中尿素的分离;实验与模拟。
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Langmuir. 2012 Jan 17;28(2):1083-94. doi: 10.1021/la201492z. Epub 2011 Dec 27.
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Scaling form of viscosity at all length-scales in poly(ethylene glycol) solutions studied by fluorescence correlation spectroscopy and capillary electrophoresis.荧光相关光谱法和毛细管电泳研究聚乙二醇溶液中所有长度尺度下的粘度标度形式。
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Spatial and temporal in situ evolution of the concentration profile during casein micelle ultrafiltration probed by small-angle X-ray scattering.通过小角X射线散射探测酪蛋白胶束超滤过程中浓度分布的时空原位演变。
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用于生物小角X射线散射的微流控透析

microfluidic dialysis for biological small-angle X-ray scattering.

作者信息

Skou Magda, Skou Søren, Jensen Thomas G, Vestergaard Bente, Gillilan Richard E

机构信息

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.

出版信息

J Appl Crystallogr. 2014 Aug 1;47(Pt 4):1355-1366. doi: 10.1107/S1600576714012618.

DOI:10.1107/S1600576714012618
PMID:25242913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4119951/
Abstract

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.

摘要

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。