Development of mass spectrometry based techniques for the identification and determination of compositional variability in recombinant polyclonal antibody products
- PMID: 20690610
- DOI: 10.1021/ac101175w
Development of mass spectrometry based techniques for the identification and determination of compositional variability in recombinant polyclonal antibody products
Abstract
Recombinant polyclonal antibodies are a new class of protein biologics, combining a defined number of target-specific antibodies, developed for therapeutic use across various indications. Development, manufacture, and release of recombinant polyclonal antibodies as well characterized biological products have required development of new chemistry, manufacturing, and control (CMC) technologies. Sym001 is a recombinant polyclonal antibody product containing 25 unique antibodies specific for the Rhesus D antigen. Sym001 drug substance is manufactured using a single batch technology, Sympress. Here, we describe the development of two novel mass spectrometry based methods that allows identification of individual antibodies in the Sym001 drug substance, through the determination of unique marker peptides or antibody light chains. The two methods provide an unambiguous identification of the 25 unique antibodies comprised in the Sym001 drug substance. Furthermore, the light chain liquid chromatography-mass spectrometry (LC-MS) method has been developed to allow the determination of the relative distribution of the 25 antibodies. The light chain LC-MS method has demonstrated linearity, specificity, precision, and accuracy, thus qualifying it for use in the quality control of recombinant polyclonal antibodies for human use. The development of such quantitative methods is central for the development and quality control of additional therapeutic recombinant polyclonal antibody products.
Similar articles
-
Identification of N-terminal modification for recombinant monoclonal antibody light chain using partial reduction and quadrupole time-of-flight mass spectrometry.Rapid Commun Mass Spectrom. 2006;20(24):3674-80. doi: 10.1002/rcm.2790. Rapid Commun Mass Spectrom. 2006. PMID: 17117408
-
Profiling of polyclonal antibody light chains by liquid chromatography/electrospray ionization mass spectrometry.Rapid Commun Mass Spectrom. 2000;14(1):49-51. doi: 10.1002/(SICI)1097-0231(20000115)14:1<49::AID-RCM828>3.0.CO;2-B. Rapid Commun Mass Spectrom. 2000. PMID: 10623928 No abstract available.
-
Production of target-specific recombinant human polyclonal antibodies in mammalian cells.Biotechnol Bioeng. 2006 Jun 5;94(2):396-405. doi: 10.1002/bit.20865. Biotechnol Bioeng. 2006. PMID: 16596663
-
Manufacture of recombinant polyclonal antibodies.Biotechnol Lett. 2007 Jun;29(6):845-52. doi: 10.1007/s10529-007-9331-8. Epub 2007 Feb 20. Biotechnol Lett. 2007. PMID: 17310321 Review.
-
Recombinant polyclonal antibodies: therapeutic antibody technologies come full circle.IDrugs. 2005 May;8(5):404-9. IDrugs. 2005. PMID: 15883923 Review.
Cited by
-
Passive immunotherapies protect WRvFire and IHD-J-Luc vaccinia virus-infected mice from lethality by reducing viral loads in the upper respiratory tract and internal organs.J Virol. 2011 Sep;85(17):9147-58. doi: 10.1128/JVI.00121-11. Epub 2011 Jun 29. J Virol. 2011. PMID: 21715493 Free PMC article.
-
Back to the future: recombinant polyclonal antibody therapeutics.Curr Opin Chem Eng. 2013 Nov;2(4):405-415. doi: 10.1016/j.coche.2013.08.005. Curr Opin Chem Eng. 2013. PMID: 24443710 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources