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Post-production protein stability: trouble beyond the cell factory

Being protein function a conformation-dependent issue, avoiding aggregation during production is a major challenge in biotechnological processes, what is often successfully addressed by convenient upstream, midstream or downstream approaches. Even when obtained in soluble forms, proteins tend to agg...

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Detalles Bibliográficos
Autores principales: Vazquez, Esther, Corchero, José Luis, Villaverde, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162505/
https://www.ncbi.nlm.nih.gov/pubmed/21806813
http://dx.doi.org/10.1186/1475-2859-10-60
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author Vazquez, Esther
Corchero, José Luis
Villaverde, Antonio
author_facet Vazquez, Esther
Corchero, José Luis
Villaverde, Antonio
author_sort Vazquez, Esther
collection PubMed
description Being protein function a conformation-dependent issue, avoiding aggregation during production is a major challenge in biotechnological processes, what is often successfully addressed by convenient upstream, midstream or downstream approaches. Even when obtained in soluble forms, proteins tend to aggregate, especially if stored and manipulated at high concentrations, as is the case of protein drugs for human therapy. Post-production protein aggregation is then a major concern in the pharmaceutical industry, as protein stability, pharmacokinetics, bioavailability, immunogenicity and side effects are largely dependent on the extent of aggregates formation. Apart from acting at the formulation level, the recombinant nature of protein drugs allows intervening at upstream stages through protein engineering, to produce analogue protein versions with higher stability and enhanced therapeutic values.
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spelling pubmed-31625052011-08-27 Post-production protein stability: trouble beyond the cell factory Vazquez, Esther Corchero, José Luis Villaverde, Antonio Microb Cell Fact Commentary Being protein function a conformation-dependent issue, avoiding aggregation during production is a major challenge in biotechnological processes, what is often successfully addressed by convenient upstream, midstream or downstream approaches. Even when obtained in soluble forms, proteins tend to aggregate, especially if stored and manipulated at high concentrations, as is the case of protein drugs for human therapy. Post-production protein aggregation is then a major concern in the pharmaceutical industry, as protein stability, pharmacokinetics, bioavailability, immunogenicity and side effects are largely dependent on the extent of aggregates formation. Apart from acting at the formulation level, the recombinant nature of protein drugs allows intervening at upstream stages through protein engineering, to produce analogue protein versions with higher stability and enhanced therapeutic values. BioMed Central 2011-08-01 /pmc/articles/PMC3162505/ /pubmed/21806813 http://dx.doi.org/10.1186/1475-2859-10-60 Text en Copyright ©2011 Vazquez et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Vazquez, Esther
Corchero, José Luis
Villaverde, Antonio
Post-production protein stability: trouble beyond the cell factory
title Post-production protein stability: trouble beyond the cell factory
title_full Post-production protein stability: trouble beyond the cell factory
title_fullStr Post-production protein stability: trouble beyond the cell factory
title_full_unstemmed Post-production protein stability: trouble beyond the cell factory
title_short Post-production protein stability: trouble beyond the cell factory
title_sort post-production protein stability: trouble beyond the cell factory
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162505/
https://www.ncbi.nlm.nih.gov/pubmed/21806813
http://dx.doi.org/10.1186/1475-2859-10-60
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