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一种用于人绒毛膜促性腺激素药物产品中 N-/O- 糖基化位点特异性定位、鉴定和定量的液相色谱 - 质谱联用一体化工作流程。

A LC-MS All-in-One Workflow for Site-Specific Location, Identification and Quantification of N-/O- Glycosylation in Human Chorionic Gonadotropin Drug Products.

作者信息

Zhu Hongbin, Qiu Chen, Ruth Ashley C, Keire David A, Ye Hongping

机构信息

Division of Pharmaceutical Analysis, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, 645 S. Newstead Ave, St. Louis, Missouri, 63110, USA.

Biotechlogic Inc., Glenview, Illinois, 60025, USA.

出版信息

AAPS J. 2017 May;19(3):846-855. doi: 10.1208/s12248-017-0062-z. Epub 2017 Feb 28.

Abstract

Site-specific characterization of the N- and O-linked glycosylation on a set of different human chorionic gonadotropin (hCG) drug products was performed by a LC-MS method combining high resolution (120K at m/z 200) mass spectrometry, multiple dissociation methods, tandem mass tag (TMT 10plex) labeling, and partial least squares-discriminant analysis (PLS-DA). In total, the data provided identification, relative quantification, and comparison of site-specific glycosylation of protein therapeutics with a single experiment. Ten different lots and/or brands of commercial therapeutic hCG were labeled with TMT 10plex reagents after tryptic digestion. The labeled intact glycopeptides were then analyzed by high resolution LC-MS with online alternating HCD/ETD/CID dissociation methods. For digested hCG drugs, 1000 intact N- and O-linked glycopeptides were identified. The relative amount of each glycopeptide from hCG products was determined based on the reporter signal intensities of the TMT labeling reagents. Moreover, with the help of TMT 10plex, through just one LC-MS run, PLS-DA was performed to ascertain the differences in glycosylation among different sources of hCG drug products. The results of PLS-DA showed that 167 glycopeptides were found to be significantly different between the naturally derived and recombinant hCG products. The results demonstrate the suitability of this method for similarity assessments and counterfeit identification of hCG as well as other glycoproteins.

摘要

采用一种液相色谱-质谱联用方法,结合高分辨率(质荷比200时为120K)质谱、多种解离方法、串联质量标签(TMT 10联)标记和偏最小二乘判别分析(PLS-DA),对一组不同的人绒毛膜促性腺激素(hCG)药品进行了N-糖基化和O-糖基化的位点特异性表征。总体而言,该数据通过一次实验实现了蛋白质治疗药物位点特异性糖基化的鉴定、相对定量和比较。对10种不同批次和/或品牌的商业治疗性hCG进行胰蛋白酶消化后,用TMT 10联试剂进行标记。然后,采用在线交替HCD/ETD/CID解离方法,通过高分辨率液相色谱-质谱对标记的完整糖肽进行分析。对于消化后的hCG药物,鉴定出1000种完整的N-糖肽和O-糖肽。根据TMT标记试剂的报告信号强度,确定hCG产品中每种糖肽的相对含量。此外,借助TMT 10联,仅通过一次液相色谱-质谱运行,就进行了PLS-DA分析,以确定不同来源hCG药品之间糖基化的差异。PLS-DA分析结果表明,天然来源的hCG产品和重组hCG产品之间有167种糖肽存在显著差异。结果表明该方法适用于hCG以及其他糖蛋白的相似性评估和假冒鉴定。

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