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Highly sialylated recombinant human erythropoietin production in large‐scale perfusion bioreactor utilizing CHO‐gmt4 (JW152) with restored GnT I function
Author(s) -
Goh John S. Y.,
Liu Yingwei,
Liu Haifeng,
Chan Kah Fai,
Wan Corrine,
Teo Gavin,
Zhou Xiangshan,
Xie Fusheng,
Zhang Peiqing,
Zhang Yuanxing,
Song Zhiwei
Publication year - 2014
Publication title -
biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.144
H-Index - 84
eISSN - 1860-7314
pISSN - 1860-6768
DOI - 10.1002/biot.201300301
Subject(s) - chinese hamster ovary cell , erythropoietin , recombinant dna , mutant , sialic acid , glycoprotein , glycosylation , chemistry , bioreactor , biochemistry , glycan , microbiology and biotechnology , biology , gene , receptor , endocrinology , organic chemistry
Therapeutic glycoprotein drugs require a high degree of sialylation of their N ‐glycans for a better circulatory half‐life that results in greater efficacy. It has been demonstrated that Chinese hamster ovary (CHO) glycosylation mutants lacking N ‐acetylglucosaminyltransferase I (GnT I), when restored by introduction of a functional GnT I, produced highly sialylated erythropoietin (EPO). We have now further engineered one of such mutants, JW152, by inactivating the dihydrofolate reductase (DHFR) gene to allow for the amplification of the EPO gene with methotrexate (MTX). Several MTX‐amplified clones maintained the ability to produce highly sialylated EPO and one was selected for culture in a perfusion bioreactor that is used in an existing industrial EPO‐production bioprocess. Extensive characterization of the EPO produced was performed using total sialic quantification, HPAEC‐PAD and MALDI‐TOF MS analyses. Our results demonstrated that the EPO produced by the mutant line exhibits superior sialylation compared to the commercially used EPO‐producing CHO clone cultured under the same conditions. Therefore, this mutant has the industrial potential for producing highly sialylated recombinant EPO and potentially other recombinant glycoprotein therapeutics.