IF 13.1 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Pei Su, John P McGee, Michael A R Hollas, Ryan T Fellers, Kenneth R Durbin, Joseph B Greer, Bryan P Early, Ping F Yip, Vlad Zabrouskov, Kristina Srzentić, Michael W Senko, Philip D Compton, Neil L Kelleher, Jared O Kafader
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引用次数: 0

摘要

单个离子质谱(I2MS)是基于 Orbitrap 的扩展质谱技术,即电荷检测质谱(CDMS)。传统的 CDMS 分析是在静电线性离子阱等内部自制仪器上进行的,而 I2MS 则将 CDMS 分析扩展到 Orbitrap 分析仪上,使广大科学界也能进行电荷检测分析。I2MS 可在一次采集过程中同时测量数百至数千个离子的质量电荷比 (m/z) 和电荷 (z),直接将光谱输出到质量域,而无需进一步解谱。可为任何所需的样品创建质量分布或 "轮廓",无论其成分或异质性如何。为了帮助将 I2MS 分析应用于实践,我们开发了这一数据采集和后续数据分析工作流程,其中包括:(i) 蛋白质样品制备;(ii) 对离子信号进行衰减以获得单个离子;(iii) 从已知电荷状态的标准蛋白质中创建电荷校准曲线;最后 (iv) 使用 STORIboard 软件从复杂或未知样品中生成有意义的质谱输出。该方案适合具有质谱分析和生物分析化学经验的用户。首先,介绍了原生和变性模式下的蛋白质标准分析,为分析传统质谱技术难以解决的复杂混合物奠定了基础。这里包含的复杂混合物实例展示了对完整人类单克隆抗体及其复杂糖基化模式的相关分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Standardized workflow for multiplexed charge detection mass spectrometry on orbitrap analyzers.

Individual ion mass spectrometry (I2MS) is the Orbitrap-based extension of the niche mass spectrometry technique known as charge detection mass spectrometry (CDMS). While traditional CDMS analysis is performed on in-house-built instruments such as the electrostatic linear ion trap, I2MS extends CDMS analysis to Orbitrap analyzers, allowing charge detection analysis to be available to the scientific community at large. I2MS simultaneously measures the mass-to-charge ratios (m/z) and charges (z) of hundreds to thousands of individual ions within one acquisition event, creating a spectral output directly into the mass domain without the need for further spectral deconvolution. A mass distribution or 'profile' can be created for any desired sample regardless of composition or heterogeneity. To assist in reducing I2MS analysis to practice, we developed this workflow for data acquisition and subsequent data analysis, which includes (i) protein sample preparation, (ii) attenuation of ion signals to obtain individual ions, (iii) the creation of a charge-calibration curve from standard proteins with known charge states and finally (iv) producing a meaningful mass spectral output from a complex or unknown sample by using the STORIboard software. This protocol is suitable for users with prior experience in mass spectrometry and bioanalytical chemistry. First, the analysis of protein standards in native and denaturing mode is presented, setting the foundation for the analysis of complex mixtures that are intractable via traditional mass spectrometry techniques. Examples of complex mixtures included here demonstrate the relevant analysis of an intact human monoclonal antibody and its intricate glycosylation patterns.

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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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