Abstract
The production of therapeutic proteins is one of the fastest growing sectors of the pharmaceutical industry. However, most proteins used in drug therapy require complex post-translational modifications for efficient secretion, drug efficacy and stability. Common protein modifications include variable glycosylation, misfolding and aggregation, oxidation of methionine, deamidation of asparagine and glutamine, and proteolysis. These modifications not only pose challenges for accurate and consistent bioprocessing, but also may have consequences for the patient in that incorrect modifications or aggregation may lead to an immune response to the protein therapeutic. This review provides examples of analytical and preventative advances that have been devised to meet these challenges, and insights into how further advances can improve the efficiency and safety in manufacturing recombinant proteins.
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Abbreviations
- ADCC:
-
antibody-dependent cellular cytotoxicity
- CHO:
-
Chinese hamster ovary
- EPO:
-
erythropoietin
- ESI-MS:
-
electrospray ionization mass spectrometry
- HPLC:
-
high pressure liquid chromatography
- MALDI:
-
matrix-assisted laser desorption-ionization
- PTM:
-
post-translational modification
- UDP:
-
uridine-5′-diphosphate
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Jenkins, N. Modifications of therapeutic proteins: challenges and prospects. Cytotechnology 53, 121–125 (2007). https://doi.org/10.1007/s10616-007-9075-2
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DOI: https://doi.org/10.1007/s10616-007-9075-2