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Native Reversed-Phase Liquid Chromatography: A Technique for LCMS of Intact Antibody-Drug Conjugates.Native 反相液相色谱法:一种用于完整抗体药物偶联物的 LCMS 的技术。
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利用红外 MALDESI 对轨道阱 240 质谱仪进行优化的 C-Trap 定时,以实现高通量筛选和天然 MS。

Optimized C-Trap Timing of an Orbitrap 240 Mass Spectrometer for High-Throughput Screening and Native MS by IR-MALDESI.

机构信息

FTMS Laboratory for Human Health Research, Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.

Precision Engineering Consortium, North Carolina State University, Raleigh, North Carolina 27695, United States.

出版信息

J Am Soc Mass Spectrom. 2022 Feb 2;33(2):328-334. doi: 10.1021/jasms.1c00319. Epub 2022 Jan 24.

DOI:10.1021/jasms.1c00319
PMID:35073091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9944060/
Abstract

Infrared matrix-assisted laser desorption ionization (IR-MALDESI) is a hybrid mass spectrometry ionization source that combines the benefits of electrospray ionization (ESI) and matrix-assisted laser desorption ionization (MALDI) making it a great analytical tool for high-throughput screening (HTS) analyses. IR-MALDESI is coupled to an Orbitrap Exploris 240 mass spectrometer that utilizes a bent quadrupole (C-trap) to inject accumulated ions into the high-field Orbitrap mass analyzer. Here, we present a study on the optimized C-trap timing for HTS analyses by IR-MALDESI mass spectrometry. The timing between initial ion generation and the C-trap opening time was optimized to reduce unnecessary ambient ion accumulation in the mass spectrometer. The time in which the C-trap was held open, the ion accumulation time, was further optimized to maximize the accumulation of analyte ions generated using IR-MALDESI. The resulting C-trap opening scheme benefits small-molecule HTS analyses by IR-MALDESI by maximizing target ion abundances, minimizing ambient ion abundances, and minimizing the total analysis time per sample. The proposed C-trap timing scheme for HTS does not translate to large molecules; a NIST monoclonal antibody standard reference material was analyzed to demonstrate that larger analytes require longer ion accumulation times and that IR-MALDESI can measure intact antibodies in their native state.

摘要

红外基质辅助激光解吸电离(IR-MALDESI)是一种混合质谱离子源,它结合了电喷雾电离(ESI)和基质辅助激光解吸电离(MALDI)的优点,使其成为高通量筛选(HTS)分析的绝佳分析工具。IR-MALDESI 与 Orbitrap Exploris 240 质谱仪耦合,该质谱仪利用弯曲四极杆(C 阱)将累积的离子注入到高场轨道阱质量分析仪中。在这里,我们研究了通过 IR-MALDESI 质谱优化 HTS 分析的 C 阱定时。优化了初始离子生成和 C 阱开启时间之间的定时,以减少质谱仪中不必要的环境离子积累。进一步优化了 C 阱保持打开的时间,即离子积累时间,以最大化使用 IR-MALDESI 生成的分析物离子的积累。所得到的 C 阱开启方案通过最大化目标离子丰度、最小化环境离子丰度和最小化每个样品的总分析时间,使小分子 HTS 分析受益。所提出的 HTS C 阱定时方案不适用于大分子;分析了 NIST 单克隆抗体标准参考物质,以证明较大的分析物需要更长的离子积累时间,并且 IR-MALDESI 可以在其天然状态下测量完整的抗体。