Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies

Proteins, which have inherent biorecognition properties, have long been used as therapeutic agents for the treatment of a wide variety of clinical indications. Protein modification through covalent attachment to different moieties improves the therapeutic’s pharmacokinetic properties, affinity, stab...

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Main Authors: Calef Sánchez-Trasviña, Miguel Flores-Gatica, Daniela Enriquez-Ochoa, Marco Rito-Palomares, Karla Mayolo-Deloisa
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2021.717326/full
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spelling doaj-6cb41d8c78014639967a40dcb27612dc2021-08-20T05:31:01ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852021-08-01910.3389/fbioe.2021.717326717326Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based StrategiesCalef Sánchez-Trasviña0Miguel Flores-Gatica1Daniela Enriquez-Ochoa2Marco Rito-Palomares3Karla Mayolo-Deloisa4Tecnologico de Monterrey, Escuela de Ingeniería y Ciencias, Centro de Biotecnología-FEMSA, Monterrey, MexicoTecnologico de Monterrey, Escuela de Ingeniería y Ciencias, Centro de Biotecnología-FEMSA, Monterrey, MexicoTecnologico de Monterrey, Escuela de Ingeniería y Ciencias, Centro de Biotecnología-FEMSA, Monterrey, MexicoTecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, MexicoTecnologico de Monterrey, Escuela de Ingeniería y Ciencias, Centro de Biotecnología-FEMSA, Monterrey, MexicoProteins, which have inherent biorecognition properties, have long been used as therapeutic agents for the treatment of a wide variety of clinical indications. Protein modification through covalent attachment to different moieties improves the therapeutic’s pharmacokinetic properties, affinity, stability, confers protection against proteolytic degradation, and increases circulation half-life. Nowadays, several modified therapeutic proteins, including PEGylated, Fc-fused, lipidated, albumin-fused, and glycosylated proteins have obtained regulatory approval for commercialization. During its manufacturing, the purification steps of the therapeutic agent are decisive to ensure the quality, effectiveness, potency, and safety of the final product. Due to the robustness, selectivity, and high resolution of chromatographic methods, these are recognized as the gold standard in the downstream processing of therapeutic proteins. Moreover, depending on the modification strategy, the protein will suffer different physicochemical changes, which must be considered to define a purification approach. This review aims to deeply analyze the purification methods employed for modified therapeutic proteins that are currently available on the market, to understand why the selected strategies were successful. Emphasis is placed on chromatographic methods since they govern the purification processes within the pharmaceutical industry. Furthermore, to discuss how the modification type strongly influences the purification strategy, the purification processes of three different modified versions of coagulation factor IX are contrasted.https://www.frontiersin.org/articles/10.3389/fbioe.2021.717326/fullchromatographypurificationPEGylationlipidationFc-fusionbiopharmaceuticals
collection DOAJ
language English
format Article
sources DOAJ
author Calef Sánchez-Trasviña
Miguel Flores-Gatica
Daniela Enriquez-Ochoa
Marco Rito-Palomares
Karla Mayolo-Deloisa
spellingShingle Calef Sánchez-Trasviña
Miguel Flores-Gatica
Daniela Enriquez-Ochoa
Marco Rito-Palomares
Karla Mayolo-Deloisa
Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
Frontiers in Bioengineering and Biotechnology
chromatography
purification
PEGylation
lipidation
Fc-fusion
biopharmaceuticals
author_facet Calef Sánchez-Trasviña
Miguel Flores-Gatica
Daniela Enriquez-Ochoa
Marco Rito-Palomares
Karla Mayolo-Deloisa
author_sort Calef Sánchez-Trasviña
title Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
title_short Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
title_full Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
title_fullStr Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
title_full_unstemmed Purification of Modified Therapeutic Proteins Available on the Market: An Analysis of Chromatography-Based Strategies
title_sort purification of modified therapeutic proteins available on the market: an analysis of chromatography-based strategies
publisher Frontiers Media S.A.
series Frontiers in Bioengineering and Biotechnology
issn 2296-4185
publishDate 2021-08-01
description Proteins, which have inherent biorecognition properties, have long been used as therapeutic agents for the treatment of a wide variety of clinical indications. Protein modification through covalent attachment to different moieties improves the therapeutic’s pharmacokinetic properties, affinity, stability, confers protection against proteolytic degradation, and increases circulation half-life. Nowadays, several modified therapeutic proteins, including PEGylated, Fc-fused, lipidated, albumin-fused, and glycosylated proteins have obtained regulatory approval for commercialization. During its manufacturing, the purification steps of the therapeutic agent are decisive to ensure the quality, effectiveness, potency, and safety of the final product. Due to the robustness, selectivity, and high resolution of chromatographic methods, these are recognized as the gold standard in the downstream processing of therapeutic proteins. Moreover, depending on the modification strategy, the protein will suffer different physicochemical changes, which must be considered to define a purification approach. This review aims to deeply analyze the purification methods employed for modified therapeutic proteins that are currently available on the market, to understand why the selected strategies were successful. Emphasis is placed on chromatographic methods since they govern the purification processes within the pharmaceutical industry. Furthermore, to discuss how the modification type strongly influences the purification strategy, the purification processes of three different modified versions of coagulation factor IX are contrasted.
topic chromatography
purification
PEGylation
lipidation
Fc-fusion
biopharmaceuticals
url https://www.frontiersin.org/articles/10.3389/fbioe.2021.717326/full
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