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使用微流控前端对溶液中的蛋白质进行高通量小角X射线散射。

High-throughput small angle X-ray scattering from proteins in solution using a microfluidic front-end.

作者信息

Toft K Nørgaard, Vestergaard Bente, Nielsen Søren S, Snakenborg Detlef, Jeppesen Mads G, Jacobsen Jes K, Arleth Lise, Kutter Jörg P

机构信息

Departments of Medicinal Chemistry, University of Copenhagen, Denmark.

出版信息

Anal Chem. 2008 May 15;80(10):3648-54. doi: 10.1021/ac800011y. Epub 2008 Apr 19.

Abstract

This manuscript presents, for the first time, the method of automated structural analysis of biomolecules in solution on a microfluidic chip. A polymer-based micrototal analysis system for high-throughput Small-Angle X-ray Scattering (SAXS) data collection from biological macromolecules has been developed. The bioXTAS chip features an integrated X-ray transparent 200 nL sample chamber and diffusion-based mixing of protein and buffer solutions. Software for fully automated fluidic control, data acquisition, and data analysis has been developed. The proof-of concept is based on data using bovine serum albumin as the model system. It confirms the quality of SAXS data generated from small sample volumes and furthermore validates the on-chip mixing capabilities. SAXS data on the gradual unfolding of BSA induced by an anionic surfactant exemplifies how the bioXTAS chip can be used to follow and identify structural changes and proves the feasibility of high-throughput structural analysis in solution. In total, this shows that the bioXTAS chip has the potential for becoming a powerful tool for automated high-throughput structural analysis of macromolecular systems.

摘要

本手稿首次展示了在微流控芯片上对溶液中的生物分子进行自动结构分析的方法。已开发出一种基于聚合物的微全分析系统,用于从生物大分子中高通量收集小角X射线散射(SAXS)数据。bioXTAS芯片具有一个集成的X射线透明200 nL样品室以及基于扩散的蛋白质和缓冲溶液混合功能。已开发出用于全自动流体控制、数据采集和数据分析的软件。概念验证基于使用牛血清白蛋白作为模型系统的数据。它证实了从小样品体积生成的SAXS数据的质量,并且进一步验证了芯片上的混合能力。由阴离子表面活性剂诱导的BSA逐渐展开的SAXS数据例证了bioXTAS芯片如何可用于跟踪和识别结构变化,并证明了溶液中高通量结构分析的可行性。总体而言,这表明bioXTAS芯片有潜力成为用于大分子系统自动高通量结构分析的强大工具。

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