Multi-Attribute Analysis of Monoclonal Antibodies Using the Agilent InfinityLab 2D-LC Solution and Q-TOF MS
Applications | 2020 | Agilent TechnologiesInstrumentation
Monoclonal antibodies (mAbs) require monitoring of multiple critical attributes during development and production. Combining affinity chromatography, size exclusion, and mass spectrometry in a single workflow addresses the complexity of mAb heterogeneity and accelerates characterization.
This study demonstrates an automated three-dimensional on-line platform that integrates protein A affinity capture for titer determination, SEC for size variant separation, and reversed-phase desalting for high-resolution mass analysis directly from cell culture supernatants.
The system uses an Agilent 1290 Infinity II 2D-LC with multiple heart-cutting valves and an Agilent 6530 Q-TOF LC/MS. The workflow comprises:
Key outcomes include:
The multi-attribute analyzer offers:
Potential advancements include:
The developed 3D on-line LC platform enables fully automated, detailed multi-attribute analysis of mAbs directly from culture supernatants with high precision and throughput, supporting accelerated biopharma development.
LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, 2D-LC
IndustriesPharma & Biopharma
ManufacturerAgilent Technologies
Summary
Significance of Multi-Attribute Analysis of Monoclonal Antibodies
Monoclonal antibodies (mAbs) require monitoring of multiple critical attributes during development and production. Combining affinity chromatography, size exclusion, and mass spectrometry in a single workflow addresses the complexity of mAb heterogeneity and accelerates characterization.
Objectives and Study Overview
This study demonstrates an automated three-dimensional on-line platform that integrates protein A affinity capture for titer determination, SEC for size variant separation, and reversed-phase desalting for high-resolution mass analysis directly from cell culture supernatants.
Methodology and Instrumentation
The system uses an Agilent 1290 Infinity II 2D-LC with multiple heart-cutting valves and an Agilent 6530 Q-TOF LC/MS. The workflow comprises:
- First dimension: Protein A affinity chromatography (pH 7.4 binding, acidic elution)
- Second dimension: Size exclusion chromatography (150 mM phosphate buffer, pH 7)
- Third dimension: RPLC desalting cartridge for salt removal
- Detection by diode array detectors at 220 and 280 nm and high-resolution MS
- Control and data processing via Agilent OpenLab CDS and MassHunter BioConfirm
Main Results and Discussion
Key outcomes include:
- Accurate mAb quantitation with linear response over 10–100 µg load
- Efficient heart-cutting reveals high- and low-molecular weight variants with ≥95.6% peak purity
- Automated capture of multiple SEC fractions in 40 µL loops for individual MS analysis
- Deconvoluted MS spectra confirm the intact mAb sequence and glycoform distribution (G0F, G1F, G2F)
- Detection of mAb dimers (∼300 kDa, 1.0%) and clipped species (3.2%)
- Excellent precision in retention times (RSD <0.2%) and peak areas (RSD <3%) over replicate runs
- Biosimilar clone screening compares originator and CHO clones, identifying a point mutation in one clone by a 68 Da mass shift
Benefits and Practical Applications
The multi-attribute analyzer offers:
- Comprehensive profiling of mAb titer, aggregation, sequence, and post-translational modifications in one run
- Streamlined workflow reducing sample handling and instrument changes
- Enhanced throughput for clone selection, process optimization, and quality control
- Applicability across research, development, and manufacturing labs
Future Trends and Application Possibilities
Potential advancements include:
- Integration of additional chromatographic modes for charge variant analysis
- AI-assisted method development and data interpretation
- High-throughput implementations for large-landscape screening
- Extension to other biotherapeutics such as fusion proteins and antibody-drug conjugates
Conclusion
The developed 3D on-line LC platform enables fully automated, detailed multi-attribute analysis of mAbs directly from culture supernatants with high precision and throughput, supporting accelerated biopharma development.
Reference
- Sandra K. et al. Modern Chromatographic and Mass Spectrometric Techniques for Protein Biopharmaceutical Characterization. J. Chromatogr. A 2014, 1335, 81–103
- Fekete S. et al. Chromatographic, Electrophoretic and Mass Spectrometric Methods for the Analytical Characterization of Protein Biopharmaceuticals. Anal. Chem. 2016, 88, 480–507
- Walsh G. Biopharmaceutical benchmarks 2018. Nat. Biotechnol. 2018, 36, 1136–1145
- Sandra K. et al. Heart-Cutting and Comprehensive Two-Dimensional Liquid Chromatography in Monoclonal Antibody Clone Selection. J. Chromatogr. A 2017, 1523, 283–292
- Stoll D. et al. Characterization of Therapeutic Antibodies and Related Products by Two-Dimensional Liquid Chromatography Coupled with UV Absorbance and Mass Spectrometric Detection. J. Chromatogr. B 2016, 1032, 51–60
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