Proteomics

Dataset Information

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Prospective ICH Q2(R2)-aligned validation of label-free untargeted proteomics for host cell protein quantification in biotherapeutics


ABSTRACT: This dataset contains raw and processed LC–MS/MS data generated for a prospective validation of label-free untargeted proteomics for host cell protein (HCP) quantification in biotherapeutic matrices. A stable isotope-labeled CHO whole-proteome standard was spiked into the NIST monoclonal antibody reference material (RM 8671) across seven concentration levels (20–80 ng total HCP per injection). Samples were analyzed using an Evosep One nanoLC system coupled to a Bruker timsTOF Pro operating in ddaPASEF mode. The study comprised four independent analytical assays totaling 198 injections and was designed to evaluate analytical performance characteristics under an ICH Q2(R2) total-error validation framework. The dataset supports evaluation of identification error control, quantitative trueness, precision, intermediate precision, and total error across the validated range. Raw Bruker timsTOF acquisition files and identification results generated with SpectroMine are provided together with the FASTA database and analysis parameters to ensure full reproducibility.

INSTRUMENT(S):

ORGANISM(S): Mus Musculus (mouse)

SUBMITTER: Somar khalil  

LAB HEAD: Somar Khalil

PROVIDER: PXD075694 | Pride | 2026-06-08

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Assay1_raw.zip Other
Pro1_Report.csv Csv
TimsTOFPro1_Entrapment_Shuffled.psar Other
TimsTOFPro1_Entrapment_Trimmed.psar Other
TimsTOFPro1_HCP_Assay1.psar Other
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Publications

Prospective ICH Q2(R2)-Aligned Total-Error Validation of Label-Free Untargeted Proteomics for Host Cell Protein Quantification in Biotherapeutics.

Khalil Somar S   Dierick Jean-François JF   Bourguignon Pascal P   Plisnier Michel M  

Proteomes 20260423 2


<b>Background</b>: Untargeted proteomics enables quantitative host cell protein (HCP) determination in biotherapeutics, yet no workflow has been validated under ICH Q2(R2) for regulated quality control. <b>Methods</b>: A prospective total-error (TE) validation of label-free ddaPASEF proteomics was performed. A stable isotope-labeled whole-proteome standard was spiked into NISTmAb at seven levels (20-80 ng) and analyzed in four independent assays (198 injections), supporting one-way random-effect  ...[more]

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