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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Mass Measurement and Top-Down HPLC/MS Analysis of Intact Monoclonal Antibodies on a Hybrid Linear Quadrupole Ion Trap-Orbitrap Mass Spectrometer
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Mass Measurement and Top-Down HPLC/MS Analysis of Intact Monoclonal Antibodies on a Hybrid Linear Quadrupole Ion Trap-Orbitrap Mass Spectrometer

机译:混合线性四极杆离子阱-轨道阱质谱仪上完整单克隆抗体的质量测量和自上而下的HPLC / MS分析

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Mass and top-down analyses of 150-kDa monoclonal immunoglobulin gamma (IgG) antibodies were performed on an Orbitrap analyzer. Three different sample delivery methods were tested including (1) infusion of an off-line desalted IgG sample using nano-electrospray; (2) on-line desalting followed by a step elution with a high percentage of organic solvent; and (3) reversed-phase HPLC separation and on-line mass and top-down analyses of disulfide isoforms of an IgG2 antibody. The accuracy of mass measurements of intact antibody was within +/-2 Da (15 ppm). The glycoforms of intact IgG antibodies separated by 162 Da were baseline resolved. In-source fragmentation of the intact antibodies produced mainly 115 residue fragments including N-terminal variable domains of heavy and light chains. The sequence coverage (the number of cleavages) was greatly increased after reduction of disulfide bonds and HPLC/MS/MS analysis of light and heavy chains using collision-induced dissociation in the ion trap of the LTQ-Orbitrap. This is an attractive alternative to peptide mapping for characterization and monitoring of post-translational modifications attributed to minimal sample preparation, high speed of the mass/top-down analysis, and relatively minor method-induced sample modifications. (J Am Soc Mass Spectrom 2009, 20, 1415-1424) (C) 2009 Published by Elsevier Inc. on behalf of American Society for Mass Spectrometry
机译:在Orbitrap分析仪上对150 kDa单克隆免疫球蛋白γ(IgG)抗体进行质量和自上而下的分析。测试了三种不同的样品传输方法,其中包括:(1)使用纳米电喷雾注入离线脱盐的IgG样品; (2)在线脱盐,然后用高百分比的有机溶剂进行逐步洗脱; (3)反相HPLC分离以及IgG2抗体二硫键同工型的在线质量和自上而下分析。完整抗体的质量测量精度在+/- 2 Da(15 ppm)之内。基线分辨了相隔162 Da的完整IgG抗体的糖型。完整抗体的源内裂解主要产生115个残基片段,包括重链和轻链的N末端可变域。减少二硫键并使用LTQ-Orbitrap离子阱中的碰撞诱导解离方法对轻链和重链进行HPLC / MS / MS分析后,序列覆盖率(裂解数)大大增加。这是肽映射的一种有吸引力的替代方法,用于表征和监测翻译后修饰,其归因于最少的样品制备,高速的质量/自上而下分析以及相对较小的方法诱导的样品修饰。 (J Am Soc Mass Spectrom 2009,20,1415-1424)(C)2009由Elsevier Inc.代表美国质谱学会出版

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