Characterization of Adeno-Associated Virus Capsid Proteins by Microflow Liquid Chromatography Coupled with Mass Spectrometry

• Published in: Applied biochemistry and biotechnology Vol. 196; no. 3; pp. 1623 - 1635
• Main Authors: Qin, Xi, Li, Xiang, Chen, Lingsheng, Gao, Tie, Luo, Ji, Guo, Lihai, Mollah, Sahana, Zhang, Zoe, Zhou, Yong, Chen, Hong-Xu
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-03-2024; Springer Nature B.V
• Subjects: Acetylation; Biochemistry; Biotechnology; Capsid protein; Capsids; Chemistry; Chemistry and Materials Science; Chromatography; Gene therapy; Immunogenicity; Infectivity; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Original Article; Oxidation; Post-translation; Proteins; Scientific imaging; Sensitivity analysis; Translation; Viruses; VP1 protein; VP3 protein; Capsid proteins; Microflow LC–MS/MS; Peptide mapping; Post-translation modification; AAV
• ISSN: 0273-2289; 1559-0291
• DOI: 10.1007/s12010-023-04656-x

Adeno-associated virus (AAV) has been widely used to treat various human diseases as an important delivery vector for gene therapy due to its low immunogenicity and safety. AAV capsids proteins are comprised of three capsid viral proteins (VP; VP1, VP2, VP3). The capsid proteins play a key role in viral vector infectivity and transduction efficiency. To ensure the safety and efficacy of AAV gene therapy products, the quality of AAV vector capsid proteins during development and production should be carefully monitored and controlled. Microflow liquid chromatography coupled with mass spectrometry provides superior sensitivity and fast analysis capability. It showed significant advantages in the analysis of low- concentration and large numbers of AAV samples. The intact mass of capsid protein can be accurately determined using high-resolution mass spectrometry (MS). And MS also provides highly confident confirmation of sequence coverage and post-translational modifications site identification and quantitation. In this study, we used microflow liquid chromatography-tandem mass spectrometry (LC–MS/MS) for the characterization of AAV2 capsid protein. we obtained nearly 100% sequence coverage of low-concentration AAV2 capsid protein (8 × 10
11
GC/mL). More than 30 post-translational modifications (PTMs) sites were identified, the PTMs types included deamidation, oxidation and acetylation. From this study, the proposed microflow LC–MS/MS method provides a sensitive and high throughput approach in the characterization of AAVs and other biological products with low abundance.