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Multi-Attribute Analysis of Monoclonal Antibodies Using the Agilent InfinityLab 2D-LC Solution and Q-TOF MS

Applications | 2020 | Agilent TechnologiesInstrumentation
LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, 2D-LC
Industries
Pharma & Biopharma
Manufacturer
Agilent 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


  1. Sandra K. et al. Modern Chromatographic and Mass Spectrometric Techniques for Protein Biopharmaceutical Characterization. J. Chromatogr. A 2014, 1335, 81–103
  2. Fekete S. et al. Chromatographic, Electrophoretic and Mass Spectrometric Methods for the Analytical Characterization of Protein Biopharmaceuticals. Anal. Chem. 2016, 88, 480–507
  3. Walsh G. Biopharmaceutical benchmarks 2018. Nat. Biotechnol. 2018, 36, 1136–1145
  4. Sandra K. et al. Heart-Cutting and Comprehensive Two-Dimensional Liquid Chromatography in Monoclonal Antibody Clone Selection. J. Chromatogr. A 2017, 1523, 283–292
  5. 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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