The Production of Complement Inhibitor Proteins in Mammalian Cell Lines-Light at the End of the Tunnel?
CR1
codon usage
complement
complement inhibitor
factor H
mRNA optimization
mammalian cell lines
recombinant protein expression
stabilon
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
14 Mar 2024
14 Mar 2024
Historique:
received:
01
02
2024
revised:
05
03
2024
accepted:
08
03
2024
medline:
28
3
2024
pubmed:
28
3
2024
entrez:
28
3
2024
Statut:
epublish
Résumé
Therapeutic recombinant proteins are powerful tools used for the treatment of many detrimental diseases such as diabetes, cancer, multiple sclerosis, rheumatoid arthritis, hepatitis, and many more. Their importance in disease therapy is growing over small molecule drugs because of their advantages like specificity and reduced side effects. However, the large-scale production of certain recombinant proteins is still challenging despite impressive advancements in biomanufacturing. The complement cascade is considered a rich source of drug targets and natural regulator proteins with great therapeutic potential. However, the versatility of such proteins has been hampered by low production rates. The recent discoveries highlighted here may bring definite improvement in the large-scale recombinant production of complement inhibitor proteins or other difficult-to-express proteins in mammalian cell lines.
Identifiants
pubmed: 38540259
pii: biomedicines12030646
doi: 10.3390/biomedicines12030646
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng