Evidence map›Paper›PMID 31169979›Full record

ArticleJournal of separation science2019

At-line multi-angle light scattering detector for faster process development in enveloped virus-like particle purification.

Patricia Pereira Aguilar, Irene González-Domínguez, Tobias Amadeus Schneider, Francesc Gòdia, Laura Cervera, Alois Jungbauer

Open access · hybridAbstract read
In one paragraph

Article in Journal of separation science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Patricia Pereira AguilarDepartment of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria.
Irene González-DomínguezDepartment d'Enginyeria Química Biològica i Ambiental, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
Tobias Amadeus SchneiderAustrian Centre of Industrial Biotechnology, Vienna, Austria.
Francesc GòdiaDepartment d'Enginyeria Química Biològica i Ambiental, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
Laura CerveraDepartment d'Enginyeria Química Biològica i Ambiental, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
Alois JungbauerDepartment of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria.ORCID https://orcid.org/0000-0001-8182-7728
Universitat Autònoma de Barcelona · ESAustrian Centre of Industrial Biotechnology (Austria) · ATBOKU University · AT

Funding

Austrian BMWD, BMVIT, SFGAustrian Science FundAustrian Science Fund FWF W 1224Government of Lower Austria and Business Agency Vienna through the Austrian FFG-COMETStandortagentur Tirol
6 · The paper itself

Abstract

At-line static light scattering and fluorescence monitoring allows direct in-process tracking of fluorescent virus-like particles. We have demonstrated this by coupling at-line multi-angle light scattering and fluorescence detectors to the downstream processing of enveloped virus-like particles. Since light scattering intensity is directly proportional to particle concentration, our strategy allowed a swift identification of product containing fractions and rapid process development. Virus-like particles containing the Human Immunodeficiency Virus-1 Gag protein fused to the Green Fluorescence protein were produced in Human Embryonic Kidney 293 cells by transient transfection. A single-column anion-exchange chromatography method was used for direct capture and purification. The majority of host-cell protein impurities passed through the column without binding. Virus-like particles bound to the column were eluted by linear or step salt gradients. Particles recovered in the step gradient purification were characterized by nanoparticle tracking analysis, size exclusion chromatography coupled to multi-angle light scattering and fluorescence detectors and transmission electron microscopy. A total recovery of 66% for the fluorescent particles was obtained with a 50% yield in the main product peak. Virus-like particles were concentrated 17-fold to final a concentration of 4.45 × 10

Indexed as

LightCells, CulturedChromatographygag Gene Products, Human Immunodeficiency VirusHEK293 CellsHumansNanoparticlesScattering, RadiationViriongag Gene Products, Human Immunodeficiency Virusenveloped bionanoparticlesfluorescent virus-like particlesmonolithsnanoparticle tracking analysis

Identifiers

PMID31169979
PMCPMC6771681
OpenAlexW2952122478

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.