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At-line High Throughput Site-specific Glycan Profiling Using Targeted Mass Spectrometry

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Specialty Biotechnology
Date 2020 Feb 20
PMID 32071892
Citations 2
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Abstract

Protein post-translational modification (PTM) plays an important role in many biological processes; of which glycosylation is arguably one of the most complex and diverse modifications and is crucial for the safety and efficacy of biotherapeutic proteins. Mass spectrometric characterization of protein glycosylation is well established with clear advantages and disadvantages; on one hand it is precise and information-rich, as well as being relative inexpensive in terms of the reagents and consumables despite the instrumentation cost and, depending on the method, can give site specific information; on the other hand it generally suffers from low throughput, restriction to largely purified samples and is less quantitative, especially for sialylated glycan species. Here, we describe a high throughput, site-specific, targeted mass spectrometric peptide mapping approach to quickly screen/rank candidate production cell lines and culture conditions that give favourable glycosylation profiles directly from conditioned culture media for an Fc-fusion protein. The methodology is fully compatible with automation and combines the speed of 'top-down' mass spectrometry with the site-specific information of 'bottom-up' mass spectrometry. In addition, this strategy can be used for multi-attribute product quality screening/monitoring as an integral part of cell line selection and process development.

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References
1.
Houel S, Hilliard M, Yu Y, McLoughlin N, Millan Martin S, Rudd P . N- and O-glycosylation analysis of etanercept using liquid chromatography and quadrupole time-of-flight mass spectrometry equipped with electron-transfer dissociation functionality. Anal Chem. 2013; 86(1):576-84. DOI: 10.1021/ac402726h. View

2.
Yang Z, Ke J, Hayes M, Bryant M, Tse F . A sensitive and high-throughput LC-MS/MS method for the quantification of pegylated-interferon-alpha2a in human serum using monolithic C18 solid phase extraction for enrichment. J Chromatogr B Analyt Technol Biomed Life Sci. 2009; 877(18-19):1737-42. DOI: 10.1016/j.jchromb.2009.04.033. View

3.
Wright A, Morrison S . Effect of altered CH2-associated carbohydrate structure on the functional properties and in vivo fate of chimeric mouse-human immunoglobulin G1. J Exp Med. 1994; 180(3):1087-96. PMC: 2191655. DOI: 10.1084/jem.180.3.1087. View

4.
Shah B, Jiang X, Chen L, Zhang Z . LC-MS/MS peptide mapping with automated data processing for routine profiling of N-glycans in immunoglobulins. J Am Soc Mass Spectrom. 2014; 25(6):999-1011. DOI: 10.1007/s13361-014-0858-3. View

5.
Hansen R, Dickson A, Goodacre R, Stephens G, Sellick C . Rapid characterization of N-linked glycans from secreted and gel-purified monoclonal antibodies using MALDI-ToF mass spectrometry. Biotechnol Bioeng. 2010; 107(5):902-8. DOI: 10.1002/bit.22879. View