Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production

The Insect Cell - Baculovirus Expression Vector System (IC-BEVS) is widely used for the production of complex recombinant (glyco)proteins. The simplicity of insect cell cultivation in suspension serum-free media and the easy construction of recombinant baculovirus vectors have made the BEVS quite an...

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Main Author: Drugmand, Jean-Christophe
Format: Others
Language:en
Published: Universite catholique de Louvain 2007
Subjects:
Online Access:http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-01032007-161307/
id ndltd-BICfB-oai-ucl.ac.be-ETDUCL-BelnUcetd-01032007-161307
record_format oai_dc
collection NDLTD
language en
format Others
sources NDLTD
topic Apoptosis
High-five
Insect cells
Metabolism
Animal cell
Process
Metabolic flux network
Physiology
Fixed-bed
Fed-batch
spellingShingle Apoptosis
High-five
Insect cells
Metabolism
Animal cell
Process
Metabolic flux network
Physiology
Fixed-bed
Fed-batch
Drugmand, Jean-Christophe
Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
description The Insect Cell - Baculovirus Expression Vector System (IC-BEVS) is widely used for the production of complex recombinant (glyco)proteins. The simplicity of insect cell cultivation in suspension serum-free media and the easy construction of recombinant baculovirus vectors have made the BEVS quite an effective expression system. On the other hand, the BEVS is a transient lytic system that may present some drawbacks in purification and potential degradation of the products. Among the various insect cell lines, the High-Five cell line has a great potential for the production of recombinant proteins using the BEVS in stirred bioreactors, reaching high cell densities and high protein production levels. Moreover, these cells can tolerate environmental stresses and can be cultivated on a large scale (Chapter 1). Unfortunately, up to now, there have been limited data available regarding suitable culture conditions and the metabolism of High-Five cells, a key requirement for the rational development of new processes. The overall goal of the present work was the study of these High-Five cells, in order to develop sophisticated new processes as alternatives to batch cultivation. The original contributions have been developed along two axes. The first axis concerns the study of the physiology and metabolism of High-Five cells. At first, we undertook a study aiming to prevent cell ring formation on suspension culture recipient walls (Chapter 2). Next, we analyzed environmental factors affecting insect cell growth and death, by comparing and developing methods able to distinguish between apoptosis and necrosis of cells (Chapter 3). The comprehensive study of the extended metabolism of High-Five cells was done using a metabolic flux network that takes account of the catabolism but also the anabolism of uninfected and baculovirus-infected cells (Chapter 4). The second axis was the application of the previously gained knowledge on High-Five cells to develop high-density systems specifically adapted to them: a fed-batch feeding strategy consisting of different pulses developed to increase the productivity of cells during infection (Chapter 5) and a fixed-bed reactor system (Chapter 6), as an alternative to classic perfusion, adapted to High-Five cells for recombinant protein production. In sum, new physiological and metabolic knowledge has been translated into new process options for High-Five cells.
author Drugmand, Jean-Christophe
author_facet Drugmand, Jean-Christophe
author_sort Drugmand, Jean-Christophe
title Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
title_short Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
title_full Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
title_fullStr Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
title_full_unstemmed Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
title_sort characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production
publisher Universite catholique de Louvain
publishDate 2007
url http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-01032007-161307/
work_keys_str_mv AT drugmandjeanchristophe characterizationofinsectcelllinesisrequiredforappropriateindustrialprocessescasestudyofhighfivecellsforrecombinantproteinproduction
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spelling ndltd-BICfB-oai-ucl.ac.be-ETDUCL-BelnUcetd-01032007-1613072013-01-07T15:42:00Z Characterization of insect cell lines is required for appropriate industrial processes : case study of high-five cells for recombinant protein production Drugmand, Jean-Christophe Apoptosis High-five Insect cells Metabolism Animal cell Process Metabolic flux network Physiology Fixed-bed Fed-batch The Insect Cell - Baculovirus Expression Vector System (IC-BEVS) is widely used for the production of complex recombinant (glyco)proteins. The simplicity of insect cell cultivation in suspension serum-free media and the easy construction of recombinant baculovirus vectors have made the BEVS quite an effective expression system. On the other hand, the BEVS is a transient lytic system that may present some drawbacks in purification and potential degradation of the products. Among the various insect cell lines, the High-Five cell line has a great potential for the production of recombinant proteins using the BEVS in stirred bioreactors, reaching high cell densities and high protein production levels. Moreover, these cells can tolerate environmental stresses and can be cultivated on a large scale (Chapter 1). Unfortunately, up to now, there have been limited data available regarding suitable culture conditions and the metabolism of High-Five cells, a key requirement for the rational development of new processes. The overall goal of the present work was the study of these High-Five cells, in order to develop sophisticated new processes as alternatives to batch cultivation. The original contributions have been developed along two axes. The first axis concerns the study of the physiology and metabolism of High-Five cells. At first, we undertook a study aiming to prevent cell ring formation on suspension culture recipient walls (Chapter 2). Next, we analyzed environmental factors affecting insect cell growth and death, by comparing and developing methods able to distinguish between apoptosis and necrosis of cells (Chapter 3). The comprehensive study of the extended metabolism of High-Five cells was done using a metabolic flux network that takes account of the catabolism but also the anabolism of uninfected and baculovirus-infected cells (Chapter 4). The second axis was the application of the previously gained knowledge on High-Five cells to develop high-density systems specifically adapted to them: a fed-batch feeding strategy consisting of different pulses developed to increase the productivity of cells during infection (Chapter 5) and a fixed-bed reactor system (Chapter 6), as an alternative to classic perfusion, adapted to High-Five cells for recombinant protein production. In sum, new physiological and metabolic knowledge has been translated into new process options for High-Five cells. Universite catholique de Louvain 2007-02-07 text application/pdf http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-01032007-161307/ http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-01032007-161307/ en unrestricted J'accepte que le texte de la thèse (ci-après l'oeuvre), sous réserve des parties couvertes par la confidentialité, soit publié dans le recueil électronique des thèses UCL. A cette fin, je donne licence à l'UCL : - le droit de fixer et de reproduire l'oeuvre sur support électronique : logiciel ETD/db - le droit de communiquer l'oeuvre au public Cette licence, gratuite et non exclusive, est valable pour toute la durée de la propriété littéraire et artistique, y compris ses éventuelles prolongations, et pour le monde entier. Je conserve tous les autres droits pour la reproduction et la communication de la thèse, ainsi que le droit de l'utiliser dans de futurs travaux. Je certifie avoir obtenu, conformément à la législation sur le droit d'auteur et aux exigences du droit à l'image, toutes les autorisations nécessaires à la reproduction dans ma thèse d'images, de textes, et/ou de toute oeuvre protégés par le droit d'auteur, et avoir obtenu les autorisations nécessaires à leur communication à des tiers. Au cas où un tiers est titulaire d'un droit de propriété intellectuelle sur tout ou partie de ma thèse, je certifie avoir obtenu son autorisation écrite pour l'exercice des droits mentionnés ci-dessus.