Literature DB >> 19786356

Analysis of reduced monoclonal antibodies using size exclusion chromatography coupled with mass spectrometry.

Hongcheng Liu1, Georgeen Gaza-Bulseco, Chris Chumsae.   

Abstract

Size-exclusion chromatography (SEC) has been widely used to detect antibody aggregates, monomer, and fragments. SEC coupled to mass spectrometry has been reported to measure the molecular weights of antibody; antibody conjugates, and antibody light chain and heavy chain. In this study, separation of antibody light chain and heavy chain by SEC and direct coupling to a mass spectrometer was further studied. It was determined that employing mobile phases containing acetonitrile, trifluoroacetic acid, and formic acid allowed the separation of antibody light chain and heavy chain after reduction by SEC. In addition, this mobile phase allowed the coupling of SEC to a mass spectrometer to obtain a direct molecular weight measurement. The application of the SEC-MS method was demonstrated by the separation of the light chain and the heavy chain of multiple recombinant monoclonal antibodies. In addition, separation of a thioether linked light chain and heavy chain from the free light chain and the free heavy chain of a recombinant monoclonal antibody after reduction was also achieved. This optimized method provided a separation of antibody light chain and heavy chain based on size and allowed a direct measurement of molecular weights by mass spectrometry. In addition, this method may help to identify peaks eluting from SEC column directly.

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Year:  2009        PMID: 19786356     DOI: 10.1016/j.jasms.2009.08.015

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  32 in total

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4.  Development and characterization of polyclonal antibody against human kappa light chain in rabbit.

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7.  Discovery and characterization of a photo-oxidative histidine-histidine cross-link in IgG1 antibody utilizing ¹⁸O-labeling and mass spectrometry.

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Review 8.  Glycan analysis of therapeutic glycoproteins.

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9.  Identification of critical chemical modifications by size exclusion chromatography of stressed antibody-target complexes with competitive binding.

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  10 in total

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