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Ligand Binding-Mass Spectrometry Methods for Understanding Macromolecular Drug Biotransformation and Impact on Immunoassay Quantification

机译:用于了解高分子药物生物转化和影响免疫测定量化的配体结合质谱法

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LBMS technology The 3 examples show that LBMS is able to track the metabolic fate of Fc fusion proteins. A high-affinity selective anti-Fc MAb concentrates the relevant analytes/metabolites and removes matrix proteins, resulting in high signal-to-noise. Top down MS of metabolites provides structural information including truncation points with time. Reduction/alkylation prior to analysis increased resolution and mass accuracy of metabolite signals. Captured metabolites can be probed by either MALDI TOF or nanoESI MS. MALDI provides a faster, simpler readout while nanoESI MS provides better resolution.
机译:LBMS技术3示例表明LBMS能够跟踪Fc融合蛋白的代谢命运。高亲和力选择性抗FC MAB浓缩相关的分析物/代谢物并除去基质蛋白质,导致高信噪比。代谢物上的顶部毫秒提供包括随时间截断点的结构信息。在分析之前还原/烷基化增加了代谢物信号的分辨率和质量准确度。可以通过MALDI TOF或纳米型MS探测捕获的代谢物。 MALDI提供更快,更简单的读数,而NanoeSi MS提供更好的分辨率。

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