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Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies

The Global Diabetes Compact was launched by the World Health Organization in April 2021 with one of its important goals to increase the accessibility and affordability of life-saving medicine—insulin. The rising prevalence of diabetes worldwide is bound to escalate the demand for recombinant insulin...

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Detalles Bibliográficos
Autores principales: Siew, Yin Yin, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313369/
https://www.ncbi.nlm.nih.gov/pubmed/34336550
http://dx.doi.org/10.1186/s40643-021-00419-w
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author Siew, Yin Yin
Zhang, Wei
author_facet Siew, Yin Yin
Zhang, Wei
author_sort Siew, Yin Yin
collection PubMed
description The Global Diabetes Compact was launched by the World Health Organization in April 2021 with one of its important goals to increase the accessibility and affordability of life-saving medicine—insulin. The rising prevalence of diabetes worldwide is bound to escalate the demand for recombinant insulin therapeutics, and currently, the majority of recombinant insulin therapeutics are produced from E. coli inclusion bodies. Here, a comprehensive review of downstream processing of recombinant human insulin/analogue production from E. coli inclusion bodies is presented. All the critical aspects of downstream processing, starting from proinsulin recovery from inclusion bodies, inclusion body washing, inclusion body solubilization and oxidative sulfitolysis, cyanogen bromide cleavage, buffer exchange, purification by chromatography, pH precipitation and zinc crystallization methods, proinsulin refolding, enzymatic cleavage, and formulation, are explained in this review. Pertinent examples are summarized and the practical aspects of integrating every procedure into a multimodal purification scheme are critically discussed. In the face of increasing global demand for insulin product, there is a pressing need to develop a more efficient and economical production process. The information presented would be insightful to all the manufacturers and stakeholders for the production of human insulins, insulin analogues or biosimilars, as they strive to make further progresses in therapeutic recombinant insulin development and production.
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spelling pubmed-83133692021-07-27 Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies Siew, Yin Yin Zhang, Wei Bioresour Bioprocess Review The Global Diabetes Compact was launched by the World Health Organization in April 2021 with one of its important goals to increase the accessibility and affordability of life-saving medicine—insulin. The rising prevalence of diabetes worldwide is bound to escalate the demand for recombinant insulin therapeutics, and currently, the majority of recombinant insulin therapeutics are produced from E. coli inclusion bodies. Here, a comprehensive review of downstream processing of recombinant human insulin/analogue production from E. coli inclusion bodies is presented. All the critical aspects of downstream processing, starting from proinsulin recovery from inclusion bodies, inclusion body washing, inclusion body solubilization and oxidative sulfitolysis, cyanogen bromide cleavage, buffer exchange, purification by chromatography, pH precipitation and zinc crystallization methods, proinsulin refolding, enzymatic cleavage, and formulation, are explained in this review. Pertinent examples are summarized and the practical aspects of integrating every procedure into a multimodal purification scheme are critically discussed. In the face of increasing global demand for insulin product, there is a pressing need to develop a more efficient and economical production process. The information presented would be insightful to all the manufacturers and stakeholders for the production of human insulins, insulin analogues or biosimilars, as they strive to make further progresses in therapeutic recombinant insulin development and production. Springer Singapore 2021-07-27 2021 /pmc/articles/PMC8313369/ /pubmed/34336550 http://dx.doi.org/10.1186/s40643-021-00419-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Siew, Yin Yin
Zhang, Wei
Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title_full Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title_fullStr Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title_full_unstemmed Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title_short Downstream processing of recombinant human insulin and its analogues production from E. coli inclusion bodies
title_sort downstream processing of recombinant human insulin and its analogues production from e. coli inclusion bodies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313369/
https://www.ncbi.nlm.nih.gov/pubmed/34336550
http://dx.doi.org/10.1186/s40643-021-00419-w
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