A Streamlined Workflow for the Characterisation and Relative Quantification of Recombinant Adeno-Associated Viruses using Charge Detection Mass Spectrometry
Posters | 2025 | Waters | ASMSInstrumentation
Recombinant adeno-associated viruses are central to gene therapy, requiring precise characterization of capsid integrity and genome packaging to ensure safety and efficacy.
This study presents a streamlined charge detection mass spectrometry workflow for assigning and quantifying empty, partial, full, and overfull rAAV capsids and compares results against mass photometry, multi-angle light scattering, and analytical ultracentrifugation.
Samples from two manufacturers were buffer-exchanged into ammonium acetate with Pluronic F-68. Ions were generated by nano-electrospray and analyzed using a prototype electrostatic linear ion trap-based CDMS. Custom waters_connect software processed time-domain signals via fast Fourier transform to extract mass-to-charge and charge information for individual ions. Additional orthogonal techniques included:
This workflow delivers rapid, high-resolution characterization of viral capsids, supports process development and quality control, and can be adapted to other biotherapeutic analytes.
Advances may include increased automation, integration with cloud-based data platforms, application to diverse viral vectors, enhanced mass resolution, and tighter coupling with orthogonal analytical methods.
The dedicated CDMS waters_connect application enables a robust, efficient, and versatile platform for detailed rAAV capsid analysis, complementing existing biophysical techniques.
No explicit literature references were provided in the source material.
LC/MS, LC/MS/MS, LC/QTRAP, Software, GPC/SEC
IndustriesPharma & Biopharma
ManufacturerWaters
Summary
Significance of the Topic
Recombinant adeno-associated viruses are central to gene therapy, requiring precise characterization of capsid integrity and genome packaging to ensure safety and efficacy.
Objectives and Study Overview
This study presents a streamlined charge detection mass spectrometry workflow for assigning and quantifying empty, partial, full, and overfull rAAV capsids and compares results against mass photometry, multi-angle light scattering, and analytical ultracentrifugation.
Methods and Instrumentation
Samples from two manufacturers were buffer-exchanged into ammonium acetate with Pluronic F-68. Ions were generated by nano-electrospray and analyzed using a prototype electrostatic linear ion trap-based CDMS. Custom waters_connect software processed time-domain signals via fast Fourier transform to extract mass-to-charge and charge information for individual ions. Additional orthogonal techniques included:
- Mass photometry (MP)
- Size-exclusion chromatography with multi-angle light scattering (SEC-MALS)
- Analytical ultracentrifugation (AUC)
Main Results and Discussion
- CDMS accurately resolved empty, intermediate, full, and overfull capsid populations and visualized them in two-dimensional heat maps.
- Relative quantification of rAAV8 empty/full ratios by CDMS agreed within 1% of combined orthogonal methods.
- CDMS demonstrated enhanced sensitivity to impurity species not readily distinguished by other techniques.
Benefits and Practical Applications
This workflow delivers rapid, high-resolution characterization of viral capsids, supports process development and quality control, and can be adapted to other biotherapeutic analytes.
Future Trends and Opportunities
Advances may include increased automation, integration with cloud-based data platforms, application to diverse viral vectors, enhanced mass resolution, and tighter coupling with orthogonal analytical methods.
Conclusion
The dedicated CDMS waters_connect application enables a robust, efficient, and versatile platform for detailed rAAV capsid analysis, complementing existing biophysical techniques.
References
No explicit literature references were provided in the source material.
Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.
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