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通过对全长腺相关病毒(AAV)衣壳蛋白进行全面的完整质量分析,开发一种快速的腺相关病毒(AAV)身份测试平台。

Development of a Rapid Adeno-Associated Virus (AAV) Identity Testing Platform through Comprehensive Intact Mass Analysis of Full-Length AAV Capsid Proteins.

作者信息

Smith Josh, Guapo Felipe, Strasser Lisa, Millán-Martín Silvia, Milian Steven G, Snyder Richard O, Bones Jonathan

机构信息

Characterisation and Comparability Laboratory, The National Institute for Bioprocessing Research and Training, Foster Avenue, Mount Merrion, Dublin A94 X099, Ireland.

Patheon Viral Vector Services, 13859 Progress Blvd, Alachua, Florida 32615, United States.

出版信息

J Proteome Res. 2023 Dec 20;23(1):161-74. doi: 10.1021/acs.jproteome.3c00513.

Abstract

Adeno-associated viruses (AAVs) are commonly used as vectors for the delivery of gene therapy targets. Characterization of AAV capsid proteins (VPs) and their post-translational modifications (PTMs) have become a critical attribute monitored to evaluate product quality. Liquid chromatography-mass spectrometry (LC-MS) analysis of intact AAV VPs provides both quick and reliable serotype identification as well as proteoform information on each VP. Incorporating these analytical strategies into rapid good manufacturing practice (GMP)-compliant workflows containing robust, but simplified, data processing methods is necessary to ensure effective product quality control (QC) during production. Here, we present a GMP-compliant LC-MS workflow for the rapid identification and in-depth characterization of AAVs. Hydrophilic interaction liquid chromatography (HILIC) MS with difluoroacetic acid as a mobile phase modifier is utilized to achieve the intact separation and identification of AAV VPs and their potential proteoforms. Peptide mapping is performed to confirm PTMs identified during intact VP analysis and for in-depth PTM characterization. The intact separations platform is then incorporated into a data processing workflow developed using GMP-compliant software capable of rapid AAV serotype identification and, if desired, specific serotype PTM monitoring and characterization. Such a platform provides product QC capabilities that are easily accessible in a regulatory setting.

摘要

腺相关病毒(AAV)通常用作递送基因治疗靶点的载体。对AAV衣壳蛋白(VP)及其翻译后修饰(PTM)进行表征已成为评估产品质量时监测的关键属性。对完整的AAV VP进行液相色谱-质谱(LC-MS)分析,既可以快速可靠地鉴定血清型,又可以提供每个VP的蛋白变体信息。将这些分析策略纳入快速的符合药品生产质量管理规范(GMP)的工作流程中,该流程包含强大但简化的数据处理方法,对于确保生产过程中的有效产品质量控制(QC)是必要的。在此,我们展示了一种用于快速鉴定和深入表征AAV的符合GMP的LC-MS工作流程。使用二氟乙酸作为流动相改性剂的亲水相互作用液相色谱(HILIC)-MS用于实现AAV VP及其潜在蛋白变体的完整分离和鉴定。进行肽图分析以确认在完整VP分析期间鉴定出的PTM,并用于深入的PTM表征。然后将完整分离平台纳入使用符合GMP的软件开发的数据处理工作流程中,该软件能够快速鉴定AAV血清型,并在需要时对特定血清型的PTM进行监测和表征。这样的平台提供了在监管环境中易于获得的产品QC能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50d0/10775144/4accfae753bf/pr3c00513_0001.jpg

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