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Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry

Adeno-associated viruses (AAV) are one of the most commonly used vehicles in gene therapies for the treatment of rare diseases. During the AAV manufacturing process, particles with little or no genetic material are co-produced alongside the desired AAV capsid containing the transgene of interest. Be...

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Autores principales: Wagner, Christina, Fuchsberger, Felix F., Innthaler, Bernd, Lemmerer, Martin, Birner-Gruenberger, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341871/
https://www.ncbi.nlm.nih.gov/pubmed/37446211
http://dx.doi.org/10.3390/ijms241311033
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author Wagner, Christina
Fuchsberger, Felix F.
Innthaler, Bernd
Lemmerer, Martin
Birner-Gruenberger, Ruth
author_facet Wagner, Christina
Fuchsberger, Felix F.
Innthaler, Bernd
Lemmerer, Martin
Birner-Gruenberger, Ruth
author_sort Wagner, Christina
collection PubMed
description Adeno-associated viruses (AAV) are one of the most commonly used vehicles in gene therapies for the treatment of rare diseases. During the AAV manufacturing process, particles with little or no genetic material are co-produced alongside the desired AAV capsid containing the transgene of interest. Because of the potential adverse health effects of these byproducts, they are considered impurities and need to be monitored carefully. To date, analytical ultracentrifugation (AUC), transmission electron microscopy (TEM) and charge-detection mass spectrometry (CDMS) are used to quantify these subspecies. However, they are associated with long turnaround times, low sample throughput and complex data analysis. Mass photometry (MP) is a fast and label-free orthogonal technique which is applicable to multiple serotypes without the adaption of method parameters. Furthermore, it can be operated with capsid titers as low as 8 × 10(10) cp mL(−1) with a CV < 5% using just 10 µL total sample volume. Here we demonstrate that mass photometry can be used as an orthogonal method to AUC to accurately quantify the proportions of empty, partially filled, full and overfull particles in AAV samples, especially in cases where ion-exchange chromatography yields no separation of the populations. In addition, it can be used to confirm the molar mass of the packaged genomic material in filled AAV particles.
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spelling pubmed-103418712023-07-14 Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry Wagner, Christina Fuchsberger, Felix F. Innthaler, Bernd Lemmerer, Martin Birner-Gruenberger, Ruth Int J Mol Sci Article Adeno-associated viruses (AAV) are one of the most commonly used vehicles in gene therapies for the treatment of rare diseases. During the AAV manufacturing process, particles with little or no genetic material are co-produced alongside the desired AAV capsid containing the transgene of interest. Because of the potential adverse health effects of these byproducts, they are considered impurities and need to be monitored carefully. To date, analytical ultracentrifugation (AUC), transmission electron microscopy (TEM) and charge-detection mass spectrometry (CDMS) are used to quantify these subspecies. However, they are associated with long turnaround times, low sample throughput and complex data analysis. Mass photometry (MP) is a fast and label-free orthogonal technique which is applicable to multiple serotypes without the adaption of method parameters. Furthermore, it can be operated with capsid titers as low as 8 × 10(10) cp mL(−1) with a CV < 5% using just 10 µL total sample volume. Here we demonstrate that mass photometry can be used as an orthogonal method to AUC to accurately quantify the proportions of empty, partially filled, full and overfull particles in AAV samples, especially in cases where ion-exchange chromatography yields no separation of the populations. In addition, it can be used to confirm the molar mass of the packaged genomic material in filled AAV particles. MDPI 2023-07-03 /pmc/articles/PMC10341871/ /pubmed/37446211 http://dx.doi.org/10.3390/ijms241311033 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wagner, Christina
Fuchsberger, Felix F.
Innthaler, Bernd
Lemmerer, Martin
Birner-Gruenberger, Ruth
Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title_full Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title_fullStr Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title_full_unstemmed Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title_short Quantification of Empty, Partially Filled and Full Adeno-Associated Virus Vectors Using Mass Photometry
title_sort quantification of empty, partially filled and full adeno-associated virus vectors using mass photometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341871/
https://www.ncbi.nlm.nih.gov/pubmed/37446211
http://dx.doi.org/10.3390/ijms241311033
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