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Innovative High-Throughput SAXS Methodologies Based on Photonic Lab-on-a-Chip Sensors: Application to Macromolecular Studies

机译:基于光子芯片实验室传感器的创新型高通量SAXS方法论:在高分子研究中的应用

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摘要

The relevance of coupling droplet-based Photonic Lab-on-a-Chip (PhLoC) platforms and Small-Angle X-Ray Scattering (SAXS) technique is here highlighted for the performance of high throughput investigations, related to the study of protein macromolecular interactions. With this configuration, minute amounts of sample are required to obtain reliable statistical data. The PhLoC platforms presented in this work are designed to allow and control an effective mixing of precise amounts of proteins, crystallization reagents and buffer in nanoliter volumes, and the subsequent generation of nanodroplets by means of a two-phase flow. Spectrophotometric sensing permits a fine control on droplet generation frequency and stability as well as on concentration conditions, and finally the droplet flow is synchronized to perform synchrotron radiation SAXS measurements in individual droplets (each one acting as an isolated microreactor) to probe protein interactions. With this configuration, droplet physic-chemical conditions can be reproducibly and finely tuned, and monitored without cross-contamination, allowing for the screening of a substantial number of saturation conditions with a small amount of biological material. The setup was tested and validated using lysozyme as a model of study. By means of SAXS experiments, the proteins gyration radius and structure envelope were calculated as a function of protein concentration. The obtained values were found to be in good agreement with previously reported data, but with a dramatic reduction of sample volume requirements compared to studies reported in the literature.
机译:本文着重介绍了基于液滴的光子芯片实验室(PhLoC)平台与小角度X射线散射(SAXS)技术的相关性,以进行与蛋白质大分子相互作用研究有关的高通量研究。使用此配置,需要微量的样品才能获得可靠的统计数据。这项工作中介绍的PhLoC平台旨在允许和控制精确量的蛋白质,结晶试剂和缓冲液以纳升体积有效混合,并通过两相流随后产生纳米液滴。分光光度传感技术可以对液滴的产生频率和稳定性以及浓度条件进行精细控制,最后对液滴流进行同步,以对单个液滴(每个作为独立的微反应器)进行同步辐射SAXS测量,以探测蛋白质相互作用。利用这种配置,可以对液滴的物理化学条件进行可重复和精细的调整,并进行监测,而不会发生交叉污染,从而可以用少量的生物材料筛选出大量的饱和条件。使用溶菌酶作为研究模型对设置进行了测试和验证。通过SAXS实验,计算出蛋白质的回转半径和结构包膜随蛋白质浓度的变化。发现所获得的值与先前报道的数据非常吻合,但是与文献报道的研究相比,样品体积的要求大大降低了。

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