Evidence map›Paper›PMID 31279895›Full record

ArticleJournal of pharmaceutical and biomedical analysis2019

Host cell protein quantification of an optimized purification method by mass spectrometry.

Karine Reiter, Motoshi Suzuki, Lisa Renee Olano, David L Narum

Open access · greenAbstract read
In one paragraph

Article in Journal of pharmaceutical and biomedical analysis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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

4 authors at 1 institution in 1 country.

Karine ReiterLaboratory of Malaria Immunology and Vaccinology, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Motoshi SuzukiResearch Technologies Branch, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, USA.
Lisa Renee OlanoResearch Technologies Branch, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, USA.
David L NarumLaboratory of Malaria Immunology and Vaccinology, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA. Electronic address: dnarum@niaid.nih.gov.
National Institute of Allergy and Infectious Diseases · US

Funding

Infectious Diseases Research Technologies Core - BethesdaZICAI001051 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$226.1M
Vaccines to Interrupt Malaria Transmission: Clinical DevelopmentZIAAI001009 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DUFFY, PATRICK · 2009 to 2025
$84.8M
Vaccine Optimization ProgramZIAAI001186 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DUFFY, PATRICK · 2013 to 2020
$1.4M
Intramural NIH HHS ZIA AI001186
6 · The paper itself

Abstract

Recombinant ExoProtein A (EPA), a detoxified form of Pseudomonas aeruginosa Exotoxin A, is used as a protein carrier in the vaccine field. A scaled manufacturing process, in which EPA was expressed in Escherichia coli, yielded a product that approached or exceeded our upper limit of E. coli host cell protein (HCP) content per human dose. The purification process was redeveloped to reduce HCP levels in the bulk product and HCP content was evaluated by orthogonal methods. Using a platform specific immunoassay, the HCP level from the original purification method was 1,830 ppm (0.18% w/w) while the revised purification process yielded the HCP below the detection limits of the assay. With a 2D/LC-MS

Indexed as

ADP Ribose TransferasesAlgorithmsAntibodies, MonoclonalBacterial ToxinsChromatography, LiquidEnzyme-Linked Immunosorbent AssayEscherichia coliExotoxinsFalse Positive ReactionsImmunoblottingProteolysisPseudomonas aeruginosa Exotoxin ARecombinant ProteinsReproducibility of ResultsTandem Mass SpectrometryVirulence FactorsADP Ribose TransferasesAntibodies, MonoclonalBacterial ToxinsExotoxinsPseudomonas aeruginosa Exotoxin ARecombinant ProteinsVirulence FactorsExoProtein AHost cell proteinsMalariaQuantitative mass spectroscopyVaccine

Identifiers

PMID31279895
PMCPMC11127253
OpenAlexW2956018847

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.