Evidence map›Paper›PMID 32994431›Full record

ArticleScientific reports2020

Microtiter plate-based antibody-competition assay to determine binding affinities and plasma/blood stability of CXCR4 ligands.

Mirja Harms, Andrea Gilg, Ludger Ständker, Ambros J Beer, Benjamin Mayer, Volker Rasche, Christian W Gruber, Jan Münch

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  13. Endogenous Peptide Inhibitors of HIV Entry.Advances in experimental medicine and biology · 2022
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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.

Mirja HarmsInstitute of Molecular Virology, Ulm University Medical Center, 89081, Ulm, Germany.
Andrea GilgInstitute of Molecular Virology, Ulm University Medical Center, 89081, Ulm, Germany.
Ludger StändkerCore Facility Functional Peptidomics, Ulm University Medical Center, 89081, Ulm, Germany.
Ambros J BeerDepartment of Nuclear Medicine, Ulm University Medical Center, 89081, Ulm, Germany.
Benjamin MayerInstitute for Epidemiology and Medical Biochemistry, Ulm University, 89081, Ulm, Germany.
Volker RascheExperimental Cardiovascular Imaging (ExCaVI), Ulm University Medical Center, 89081, Ulm, Germany.
Christian W GruberInstitute of Pharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, 1090, Vienna, Austria.
Jan MünchInstitute of Molecular Virology, Ulm University Medical Center, 89081, Ulm, Germany. jan.muench@uni-ulm.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C-X-C chemokine receptor type 4 (CXCR4) is involved in several intractable disease processes, including HIV infection, cancer cell metastasis, leukemia cell progression, rheumatoid arthritis, asthma and pulmonary fibrosis. Thus, CXCR4 represents a promising drug target and several CXCR4 antagonizing agents are in preclinical or clinical development. Important parameters in drug lead evaluation are determination of binding affinities to the receptor and assessment of their stability and activity in plasma or blood of animals and humans. Here, we designed a microtiter plate-based CXCR4 antibody competition assay that enables to measure inhibitory concentrations (IC

Indexed as

AdultAnimalsAntibodiesAntibody AffinityFemaleHealthy VolunteersHumansInhibitory Concentration 50LigandsMaleMiceMice, Inbred C57BLPlasmaReceptors, CXCR4Signal TransductionAntibodiesCXCR4 protein, humanLigandsReceptors, CXCR4

Identifiers

PMID32994431
PMCPMC7525492

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Registered trials

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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.