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Implementing Fast Photochemical Oxidation of Proteins (FPOP) as a Footprinting Approach to Solve Diverse Problems in Structural Biology

机译:实施蛋白质快速光化学氧化(FPOP)作为解决结构生物学中各种问题的足迹方法

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摘要

Fast photochemical oxidation of proteins (FPOP) is a footprinting technique used in mass spectrometry-based structural proteomics. It has been applied to solve a variety of problems in different areas of biology. A FPOP platform requires a laser, optics, and sample flow path properly assembled to enable fast footprinting. Sample preparation, buffer conditions, and reagent concentrations are essential to obtain reasonable oxidations on proteins. FPOP samples can be analyzed by LC-MS methods to measure the modification extent, which is a function of the solvent-accessible surface area of the protein. The platform can be expanded to accommodate several new approaches, including dose responsible studies, new footprinting reagents, and two-laser pump-probe experiments. Here, we briefly review FPOP applications and in a detailed manner describe the procedures to set up an FPOP protein footprinting platform.
机译:蛋白质的快速光化学氧化(FPOP)是一种用于基于质谱的结构蛋白质组学的足迹技术。它已被用于解决生物学不同领域的各种问题。 FPOP平台需要正确组装的激光器,光学器件和样品流路,以实现快速覆盖。样品制备,缓冲液条件和试剂浓度对于在蛋白质上获得合理的氧化至关重要。可以通过LC-MS方法分析FPOP样品,以测量修饰程度,该程度是蛋白质可接触溶剂的表面积的函数。该平台可以扩展以适应几种新方法,包括剂量负责的研究,新的足迹试剂和两激光泵浦探针实验。在这里,我们简要回顾FPOP应用程序,并以详细的方式描述建立FPOP蛋白足迹平台的过程。

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