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Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents

Adeno-associated viruses (AAVs) are one of the most promising tools for gene therapy applications. These vectors are purified using affinity and ion exchange chromatography, typically using packed beds of resin adsorbents. This leads to diffusion and pressure drop limitations that affect process pro...

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Autores principales: Neto, Salomé, Mendes, João P., Santos, Susana B. Dos, Solbrand, Anita, Carrondo, Manuel J. T., Peixoto, Cristina, Silva, Ricardo J. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229133/
https://www.ncbi.nlm.nih.gov/pubmed/37260828
http://dx.doi.org/10.3389/fbioe.2023.1183974
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author Neto, Salomé
Mendes, João P.
Santos, Susana B. Dos
Solbrand, Anita
Carrondo, Manuel J. T.
Peixoto, Cristina
Silva, Ricardo J. S.
author_facet Neto, Salomé
Mendes, João P.
Santos, Susana B. Dos
Solbrand, Anita
Carrondo, Manuel J. T.
Peixoto, Cristina
Silva, Ricardo J. S.
author_sort Neto, Salomé
collection PubMed
description Adeno-associated viruses (AAVs) are one of the most promising tools for gene therapy applications. These vectors are purified using affinity and ion exchange chromatography, typically using packed beds of resin adsorbents. This leads to diffusion and pressure drop limitations that affect process productivity. Due to their high surface area and porosity, electrospun nanofiber adsorbents offer mass transfer and flow rate advantages over conventional chromatographic media. The present work investigated the use of affinity cellulose-based nanofiber adsorbents for adeno-associated virus serotype 5 (AAV5) capture, evaluating dynamic binding capacity, pressure drop, and AAV5 recovery at residence times (RT) less than 5 s. The dynamic binding capacity was found to be residence time-dependent, but nevertheless higher than 1.0 × 10(14) TP mL(−1) (RT = 1.6 s), with a pressure drop variation of 0.14 MPa obtained after loading more than 2,000 column volumes of clarified AAV5 feedstock. The single affinity chromatography purification step using these new affinity adsorbents resulted in 80% virus recovery, with the removal of impurities comparable to that of bead-based affinity adsorbents. The high binding capacity, virus recovery and reduced pressure drop observed at residence times in the sub-minute range can potentially eliminate the need for prior concentration steps, thereby reducing the overall number of unit operations, process time and costs.
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spelling pubmed-102291332023-05-31 Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents Neto, Salomé Mendes, João P. Santos, Susana B. Dos Solbrand, Anita Carrondo, Manuel J. T. Peixoto, Cristina Silva, Ricardo J. S. Front Bioeng Biotechnol Bioengineering and Biotechnology Adeno-associated viruses (AAVs) are one of the most promising tools for gene therapy applications. These vectors are purified using affinity and ion exchange chromatography, typically using packed beds of resin adsorbents. This leads to diffusion and pressure drop limitations that affect process productivity. Due to their high surface area and porosity, electrospun nanofiber adsorbents offer mass transfer and flow rate advantages over conventional chromatographic media. The present work investigated the use of affinity cellulose-based nanofiber adsorbents for adeno-associated virus serotype 5 (AAV5) capture, evaluating dynamic binding capacity, pressure drop, and AAV5 recovery at residence times (RT) less than 5 s. The dynamic binding capacity was found to be residence time-dependent, but nevertheless higher than 1.0 × 10(14) TP mL(−1) (RT = 1.6 s), with a pressure drop variation of 0.14 MPa obtained after loading more than 2,000 column volumes of clarified AAV5 feedstock. The single affinity chromatography purification step using these new affinity adsorbents resulted in 80% virus recovery, with the removal of impurities comparable to that of bead-based affinity adsorbents. The high binding capacity, virus recovery and reduced pressure drop observed at residence times in the sub-minute range can potentially eliminate the need for prior concentration steps, thereby reducing the overall number of unit operations, process time and costs. Frontiers Media S.A. 2023-05-16 /pmc/articles/PMC10229133/ /pubmed/37260828 http://dx.doi.org/10.3389/fbioe.2023.1183974 Text en Copyright © 2023 Neto, Mendes, Santos, Solbrand, Carrondo, Peixoto and Silva. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Neto, Salomé
Mendes, João P.
Santos, Susana B. Dos
Solbrand, Anita
Carrondo, Manuel J. T.
Peixoto, Cristina
Silva, Ricardo J. S.
Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title_full Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title_fullStr Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title_full_unstemmed Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title_short Efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
title_sort efficient adeno-associated virus serotype 5 capture with affinity functionalized nanofiber adsorbents
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229133/
https://www.ncbi.nlm.nih.gov/pubmed/37260828
http://dx.doi.org/10.3389/fbioe.2023.1183974
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