Targeted Quantification of High-Risk HCPs in CHO

Accurate and reproducible quantification of 90+ CHO Host Cell Proteins using targeted LC-MS/MS and isotope-labelled peptides.

ANAQUANT’s targeted LC-MS/MS platform.

  • More than 90 CHO HCPs

  • Isotope-labeled peptide standards

  • At each step of the DownStream Process (DSP)

  • High Sensitivity & Robustness

  • Coverage of >90 CHO HCPs identified as high-risk

  • Selection of specific Isotope-labeled peptide standards for each target

  • Compatible with in-process, intermediate, or drug substance samples

  • Optimized LC-MS/MS workflow using labeled peptide standards for absolute quantification.


Targeted Quantification of High-Risk HCPs in CHO-Based Biotherapeutics

During bioproduction in CHO cells, residual Host Cell Proteins (HCPs) can remain in the final drug substance despite purification steps. While most HCPs are harmless, a subset of critical or high-risk HCPs may compromise product safety, efficacy, or stability. These include enzymes capable of degrading the therapeutic protein, proteases, lipases and immunogenic contaminants.

ANAQUANT has developed a targeted proteomic method based on stable isotope-labeled peptides to quantify over 90 high-risk CHO HCPs identified from literature and regulatory alerts.
Using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS), our method enables precise and multiplexed quantification of the most critical residual proteins in a single analytical run.

Each peptide has been carefully selected and validated to ensure specificity, linearity, and reproducibility, allowing reliable quantification even at trace levels (ng/mg range).

Bioprocess development

  • > Evaluate purification efficiency and clearance of high-risk HCPs.

Comparability studies

  • > Monitor consistency across production batches.

Regulatory submissions

  • > Strengthen your impurity profile with quantitative, validated data.

Risk assessment studies

  • > Characterize and mitigate critical HCPs that could affect product stability or immunogenicity.