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Quantitative correlation between transcriptional levels of ER chaperone, peroximal protein and FVIII productivity in human Hek-293 cell line.


ABSTRACT: Hek-293 cell line presents good production platform for recombinant therapeutic proteins, however little is known about the components that contribute to the cellular control of recombinant protein production. In this study, we generated a Hek-293 producing recombinant factor VIII (FVIII) and we evaluated the immunoglobulin-binding protein (BiP) and phytanoil-CoA ?-hydroxylase (PAHX) expression levels which are known for diminishing FVIII production. Our analyses showed that the recombinant cell population expresses 3.1 ± 1.4 fold of BIP mRNA (P?=?0.0054) and 97.8 ± 0.5 fold of PAHX mRNA (P?=?0.0016) compared to nontransduced cells. The amount of these proteins was inversely correlated to the secreted FVIII. In conclusion, BIP and PAHX expression are augmented in human cells producing FVIII and they antagonize the amount of therapeutic factor VIII in the cell culture.

SUBMITTER: Rodrigues ES 

PROVIDER: S-EPMC4255388 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Quantitative correlation between transcriptional levels of ER chaperone, peroximal protein and FVIII productivity in human Hek-293 cell line.

Rodrigues Evandra Strazza ES   Picanço-Castro Virgínia V   Espanhol Marta Regina MR   de Andrade Luiz Alberto Martins LA   Palma Patricia Vianna Bonini PV   Kashima Simone S   Fontes Aparecida Maria AM   Covas Dimas Tadeu DT  

SpringerPlus 20130718


Hek-293 cell line presents good production platform for recombinant therapeutic proteins, however little is known about the components that contribute to the cellular control of recombinant protein production. In this study, we generated a Hek-293 producing recombinant factor VIII (FVIII) and we evaluated the immunoglobulin-binding protein (BiP) and phytanoil-CoA α-hydroxylase (PAHX) expression levels which are known for diminishing FVIII production. Our analyses showed that the recombinant cell  ...[more]

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