Evidence map›Paper›PMID 39282080›Full record

ArticleMolecular therapy. Methods & clinical development2024

Assessment of adeno-associated virus purity by capillary electrophoresis-based western.

Julyana Acevedo, Yiling Bi, Jessica Gee, Santoshkumar L Khatwani

Erratum issuedAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

5 · Who and what money

Authors and funding

4 authors.

Julyana AcevedoAnalytical Development, Sangamo Therapeutics, 501 Canal Blvd, Richmond, CA 94804, USA.
Yiling BiAnalytical Development, Sangamo Therapeutics, 501 Canal Blvd, Richmond, CA 94804, USA.
Jessica GeeAnalytical Development, Sangamo Therapeutics, 501 Canal Blvd, Richmond, CA 94804, USA.
Santoshkumar L KhatwaniAnalytical Development, Sangamo Therapeutics, 501 Canal Blvd, Richmond, CA 94804, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A rigorous analytical assessment of recombinant adeno-associated virus (rAAV)-based drug products is critical for their successful development as clinical candidates. It is especially important to ascertain high purity while simultaneously ensuring low levels of impurities in the final drug product. One approach to evaluate the purity of rAAV drug products is to determine the relative stoichiometry of the three viral proteins (VPs) that comprise an rAAV capsid, and the levels of impurities in the final drug product. Here we present two capillary electrophoresis-western (CE-western) assays for quantifying (1) the relative stoichiometry of VP using the anti-AAV B1 antibody, and (2) residual levels of a baculovirus protein impurity, GP64, using the anti-GP64 antibody. In each assay, various purified samples from diverse AAV serotypes were analyzed to determine their VP ratio or GP64 levels. The ratio of VP3/VP1 in rAAV samples was correlated with biological activity, and the clearance of GP64 from the manufacturing process was demonstrated. The results obtained from both assays were further supported by liquid chromatography-mass spectrometry analyses. Overall, we report that CE-western is a high-throughput platform that utilizes low sample volumes for a rapid, sensitive, and robust assessment of the identity, composition, and purity of rAAV drug products.

Indexed as

AAVAcMNPVadeno-associated viruscapillary electrophoresisCE-westernGP64LC-MSresidual baculovirus proteinviral protein ratioVP ratio

Identifiers

PMID39282080
PMCPMC11396060

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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.