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Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS

Adeno-associated virus (AAV) has emerged as a leading platform for gene therapy. With the skyrocketing rate of AAV research and the prevalence of many new engineered capsids being investigated in preclinical and clinical trials, capsid characterization plays a vital role in serotype confirmation and...

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Autores principales: Lam, Anh K., Zhang, Junping, Frabutt, Dylan, Mulcrone, Patrick L., Li, Lei, Zeng, Lifan, Herzog, Roland W., Xiao, Weidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563341/
https://www.ncbi.nlm.nih.gov/pubmed/36284765
http://dx.doi.org/10.1016/j.omtm.2022.09.008
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author Lam, Anh K.
Zhang, Junping
Frabutt, Dylan
Mulcrone, Patrick L.
Li, Lei
Zeng, Lifan
Herzog, Roland W.
Xiao, Weidong
author_facet Lam, Anh K.
Zhang, Junping
Frabutt, Dylan
Mulcrone, Patrick L.
Li, Lei
Zeng, Lifan
Herzog, Roland W.
Xiao, Weidong
author_sort Lam, Anh K.
collection PubMed
description Adeno-associated virus (AAV) has emerged as a leading platform for gene therapy. With the skyrocketing rate of AAV research and the prevalence of many new engineered capsids being investigated in preclinical and clinical trials, capsid characterization plays a vital role in serotype confirmation and quality control. Further, peptide mapping the capsid proteins might inevitably be a future requirement by regulatory agencies since it is a critical step in good manufacturing practice (GMP) for biotherapeutic characterization. To overcome many challenges that traditional methods like SDS-PAGE and western blots carry, liquid chromatography and mass spectrometry (LC-MS) allows high resolution and sensitivity with great accuracy in characterizing the AAV capsid proteins. Our optimized LC-MS method provides quick sample preparation, a fast and high-throughput 4-min run, and high sensitivity, which allows for very efficient characterization of wild-type and engineered capsids. This study also reports the usage of LC-MS/MS peptide mapping of AAV capsid proteins to determine the most accessible lysine residues targeted by chemical modifications. Our detailed protocols are anticipated to promote the development and discovery of AAV variants with high accuracy and efficiency.
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spelling pubmed-95633412022-10-24 Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS Lam, Anh K. Zhang, Junping Frabutt, Dylan Mulcrone, Patrick L. Li, Lei Zeng, Lifan Herzog, Roland W. Xiao, Weidong Mol Ther Methods Clin Dev Original Article Adeno-associated virus (AAV) has emerged as a leading platform for gene therapy. With the skyrocketing rate of AAV research and the prevalence of many new engineered capsids being investigated in preclinical and clinical trials, capsid characterization plays a vital role in serotype confirmation and quality control. Further, peptide mapping the capsid proteins might inevitably be a future requirement by regulatory agencies since it is a critical step in good manufacturing practice (GMP) for biotherapeutic characterization. To overcome many challenges that traditional methods like SDS-PAGE and western blots carry, liquid chromatography and mass spectrometry (LC-MS) allows high resolution and sensitivity with great accuracy in characterizing the AAV capsid proteins. Our optimized LC-MS method provides quick sample preparation, a fast and high-throughput 4-min run, and high sensitivity, which allows for very efficient characterization of wild-type and engineered capsids. This study also reports the usage of LC-MS/MS peptide mapping of AAV capsid proteins to determine the most accessible lysine residues targeted by chemical modifications. Our detailed protocols are anticipated to promote the development and discovery of AAV variants with high accuracy and efficiency. American Society of Gene & Cell Therapy 2022-09-24 /pmc/articles/PMC9563341/ /pubmed/36284765 http://dx.doi.org/10.1016/j.omtm.2022.09.008 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Lam, Anh K.
Zhang, Junping
Frabutt, Dylan
Mulcrone, Patrick L.
Li, Lei
Zeng, Lifan
Herzog, Roland W.
Xiao, Weidong
Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title_full Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title_fullStr Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title_full_unstemmed Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title_short Fast and high-throughput LC-MS characterization, and peptide mapping of engineered AAV capsids using LC-MS/MS
title_sort fast and high-throughput lc-ms characterization, and peptide mapping of engineered aav capsids using lc-ms/ms
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563341/
https://www.ncbi.nlm.nih.gov/pubmed/36284765
http://dx.doi.org/10.1016/j.omtm.2022.09.008
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