Evidence map›Paper›PMID 40721212›Full record

ArticleJournal of the American Society for Mass Spectrometry2025

Accelerating Characterization of Therapeutic Antibodies: A Comparative Assessment of icIEF-UV/MS and the Traditional Fractionation Workflow.

Arnik Shah, Parth Shah, Alex Johnson, Jean Bender, Dmitry Gumerov, Jingwen Ding, Scott Mack, Matthew D Stone, Maggie A Ostrowski

Abstract readComparative Study
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Arnik ShahVisterra Inc, 275 second avenue, Waltham, Massachusetts 02451, United States.ORCID 0000-0003-3455-0177
Parth ShahVisterra Inc, 275 second avenue, Waltham, Massachusetts 02451, United States.
Alex JohnsonVisterra Inc, 275 second avenue, Waltham, Massachusetts 02451, United States.
Jean BenderVisterra Inc, 275 second avenue, Waltham, Massachusetts 02451, United States.
Dmitry GumerovVisterra Inc, 275 second avenue, Waltham, Massachusetts 02451, United States.
Jingwen DingSCIEX, Fremont, California 94538, United States.
Scott MackSCIEX, Fremont, California 94538, United States.
Matthew D StoneSCIEX, Fremont, California 94538, United States.
Maggie A OstrowskiSCIEX, Fremont, California 94538, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate characterization of charge variants in biologics is crucial to uphold stringent quality standards ensuring the safety and efficacy of biotherapeutic products and regulatory requirements for the Biologic Licensing Application (BLA) process enabling marketing application. These variants, arising from post-translational modifications (PTMs) during upstream processing and enzymatic/nonenzymatic reactions in downstream processing and storage, can significantly impact therapeutic potency, efficacy, and immunogenicity. Conventional methods for characterizing charge variants typically involve labor-intensive fraction enrichment, consuming time and resources. However, recent technological advancements, exemplified by the Intabio ZT system's innovative platform, enable the seamless and direct integration of imaged capillary isoelectric focusing (icIEF) and UV quantitation with mass spectrometry (MS) PTM identification, facilitating rapid and unbiased characterization. In this study, we conduct a comparative assessment of the charge variant characterization of investigative mAb-1 using icIEF-UV/MS analysis and a traditional fractionation-based workflow. Our results demonstrated that icIEF-UV/MS-based proteoform characterization provided comparable icIEF-UV separation and quantitation and superior direct MS-based peak characterization with shorter time and less sample processing compared to conventional fractionation approaches.

Indexed as

Antibodies, MonoclonalMass SpectrometryCapillary Isoelectric FocusingElectrophoresis, CapillaryHumansIsoelectric FocusingProtein Processing, Post-TranslationalWorkflowAntibodies, MonoclonalBiologic licensing applicationBiologicsCharge variant characterizationImaged capillary isoelectric focusing (icIEF)Mass spectrometry (MS)Post-translational modifications (PTMs)

Identifiers

PMID40721212
PMCPMC12333362

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.