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在毛细管电泳-质谱联用中,通过动态 pH 阻断连接聚焦氨基酸、肽和酶解的单克隆抗体。

Dynamic pH barrage junction focusing of amino acids, peptides, and digested monoclonal antibodies in capillary electrophoresis-mass spectrometry.

机构信息

Department of Chemistry, University of British Columbia, Vancouver, BC, Canada.

BC Cancer Research Center, Vancouver, BC, Canada.

出版信息

Electrophoresis. 2020 Nov;41(21-22):1832-1842. doi: 10.1002/elps.202000076. Epub 2020 Jun 3.

Abstract

Dynamic pH barrage junction focusing in CE enables effective signal enhancement, quantitative capture efficiencies, and straightforward optimization. The method is a technical variant of dynamic pH junction focusing. CE separation with dynamic pH barrage junction focusing is compatible with both optical and mass spectrometric detection. We developed a CE-MS/MS method using hydrophilic polyethyleneimine-coated capillaries and validated it for the qualitative analysis of amino acids, peptides, and tryptic peptides of digested monoclonal antibodies. The S/N of extracted ion electropherograms of zwitterionic analytes were enhanced by approximately two orders of magnitude with a tradeoff of a shortened separation window. Online focusing improved the MS signal intensity of a diluted antibody digest, enabling more precursor ions to be analyzed with subsequent tandem mass spectrometric identification. It also broadened the concentration range of protein digest samples for which adequate sequence coverage data can be obtained. With only 0.9 ng of digested infliximab sample loaded into the capillary, 76% and 100% sequence coverage was realized for antibody heavy and light chains, respectively, after online focusing. Full coverage was achieved with 9 ng of injected digest.

摘要

在 CE 中,动态 pH 垒聚焦实现了有效的信号增强、定量的捕获效率和简单的优化。该方法是动态 pH 结聚焦的技术变体。CE 分离与动态 pH 垒聚焦兼容,适用于光学和质谱检测。我们开发了一种使用亲水聚乙烯亚胺涂层毛细管的 CE-MS/MS 方法,并对其进行了验证,用于定性分析氨基酸、肽和消化后的单克隆抗体的酶切肽段。带电荷分析物的提取离子电泳图谱的 S/N 通过大约两个数量级的增强,以牺牲较短的分离窗口为代价。在线聚焦提高了稀释抗体消化物的 MS 信号强度,使得更多的前体离子可以进行后续的串联质谱鉴定。它还拓宽了蛋白质消化样品的浓度范围,从而可以获得足够的序列覆盖数据。仅将 0.9ng 的消化后的英夫利昔单抗样品加载到毛细管中,在线聚焦后,抗体重链和轻链的序列覆盖率分别达到 76%和 100%。在注射消化物 9ng 时实现了完全覆盖。

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