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High-level production and purification of bioactive recombinant human activin A in Chinese hamster ovary cells

  • Changin Kim
  • , Hyunjoo Kim
  • , Jeong Soo Park
  • , Jiwon Park
  • , Jeongmin Oh
  • , Jaeseung Yoon
  • , Kwanghee Baek

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Activin A, a member of the TGF-β superfamily, is a homodimer of the inhibin βΑ subunit that plays a diversity of roles in biological processes. Because of its multiple functions, significant efforts have been made to produce activin A, however, unsatisfactory results were obtained due to its low level of expression. In this study, a stable CHO cell line exhibiting high expression of rhActivin A was isolated and production of rhActivin A was achieved using the cell line from 11-day fed-batch cultures in a 7.5 L bioreactor. The production rate was 0.22 g/L, substantially higher than those reported in previous studies. The culture supernatant of the bioreactor was used to purify rhActivin A (purity: >99%, recovery rate: 47%). The purified rhActivin A exhibited biological activity, with an EC50 of 3.893 ng/mL and a specific activity of 1.38 × 103IU/mg. The control of process-related impurities in the purified rhActivin A was successful and met the USP recommendations for use in cell therapy. Thus, our production and purification methods were appropriate for large-scale GMP-grade rhActivin A production, which can be used for various purposes including cell therapy.

Original languageEnglish
Pages (from-to)218-225
Number of pages8
JournalPreparative Biochemistry and Biotechnology
Volume54
Issue number2
DOIs
Publication statusPublished - 2024

Bibliographical note

Publisher Copyright:
© 2023 Taylor & Francis Group, LLC.

Keywords

  • Activin A
  • Chinese hamster ovary (CHO) cells
  • USP
  • bioassay
  • purification
  • recombinant protein expression

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