Evidence map›Paper›PMID 37160443›Full record

ArticleEuropean biophysics journal : EBJ2023

Sedimentation velocity FDS studies of antibodies in pooled human serum.

J J Correia, G R Bishop, P B Kyle, R T Wright, P J Sherwood, W F Stafford

Abstract read
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In one paragraph

Article in European biophysics journal : EBJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 5 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 4 institutions in 1 country.

J J CorreiaDepartment of Cell and Molecular Biology, University of Miss Medical Center, Jackson, MS, USA. jcorreia@umc.edu.ORCID http://orcid.org/0000-0002-6885-7508
G R BishopDepartment of Pharmacology and Toxicology, University of Miss Medical Center, Jackson, MS, USA.
P B KyleDepartment of Pathology, University of Miss Medical Center, Jackson, MS, USA.
R T WrightJanssen Research and Development, Spring House, PA, 19477, USA.
P J SherwoodInteractive Technology, Oakland, CA, USA.
W F StaffordDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.
University of Mississippi Medical Center · USHarvard University · USJackson Memorial Hospital · USJanssen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biotech industry has great interest in investigating therapeutic proteins in high concentration environments like human serum. The fluorescence detection system (Aviv-FDS) allows the performance of analytical ultracentrifuge (AUC) sedimentation velocity (SV) experiments in tracer or BOLTS protocols. Here, we compare six pooled human serum samples by AUC SV techniques and demonstrate the potential of this technology for characterizing therapeutic antibodies in serum. Control FDS SV experiments on serum alone reveal a bilirubin-HSA complex whose sedimentation is slowed by solution nonideality and exhibits a Johnston-Ogston (JO) effect due to the presence of high concentrations of IgG. Absorbance SV experiments on diluted serum samples verify the HSA-IgG composition as well as a significant IgM pentamer boundary at 19 s. Alexa-488 labeled Simponi (Golimumab) is used as a tracer to investigate the behavior of a therapeutic monoclonal antibody (mAb) in serum, and the sedimentation behavior of total IgG in serum. Serum dilution experiments allow extrapolation to zero concentration to extract s

Indexed as

Immunoglobulin GFluorescenceHumansImmunoglobulin MUltracentrifugationImmunoglobulin GImmunoglobulin MFluorescence detection systemHydrodynamic nonidealityJohnston–Ogston effectSedimentation velocityThermodynamic nonideality

Identifiers

PMID37160443
OpenAlexW4376109943

What OpenQuestion holds

Textmetadata
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.