Evidence map›Paper›PMID 31223185›Full record

ArticleJournal of membrane science2019

DNA RETENTION ON DEPTH FILTERS.

Ohnmar Khanal, Xuankuo Xu, Nripen Singh, Steven J Traylor, Chao Huang, Sanchayita Ghose, Zheng Jian Li, Abraham M Lenhoff

Abstract read
In one paragraph

Article in Journal of membrane science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 23 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

8 authors at 2 institutions in 1 country.

Ohnmar KhanalDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19716, USA.
Xuankuo XuBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Nripen SinghBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Steven J TraylorBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Chao HuangBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Sanchayita GhoseBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Zheng Jian LiBiologics Process Development, Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, MA 01434, USA.
Abraham M LenhoffDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19716, USA.
Bristol-Myers Squibb (United States) · USUniversity of Delaware · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
NIGMS NIH HHS P20 GM103446
6 · The paper itself

Abstract

Depth filtration is a commonly-used bioprocessing unit operation for harvest clarification that reduces the levels of process- and product-related impurities such as cell debris, host-cell proteins, nucleic acids and protein aggregates. Since depth filters comprise multiple components, different functionalities may contribute to such retention, making the mechanisms by which different impurities are removed difficult to decouple. Here we probe the mechanisms by which double-stranded DNA (dsDNA) is retained on depth filter media by visualizing the distribution of fluorescently-labeled retained DNA on spent depth filter discs using confocal fluorescence microscopy. The extent of DNA displacement into the depth filter was found to increase with decreasing DNA length with increasing operational parameters such as wash volume and buffer ionic strength. Finally, using 5ethynyl-2'-deoxyuridine (EdU) to label DNA in dividing CHO cells, we showed that Chinese hamster ovary (CHO) cellular DNA in the lysate supernatant migrates deeper into the depth filter than the lysate re-suspended pellet, elucidating the role of the size of the DNA in its form as an impurity. Apart from aiding DNA purification and removal, our experimental approaches and findings can be leveraged in studying the transport and retention of nucleic acids and other impurities on depth filters at a small scale.

Indexed as

adsorptiondepth filtrationDNA oligosgenomic DNAretention

Identifiers

PMID31223185
PMCPMC6586439
OpenAlexW2898433893

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.