Evidence map›Paper›PMID 23576004›Full record

ArticleJournal of fluorescence2013

Detection of target proteins by fluorescence anisotropy.

Lin Wang, Brendan Clifford, Lacey Graybeal, Luke Tolley, Matthew E McCarroll

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of fluorescence, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Lin WangDepartment of Chemistry and Biochemistry, Southern Illinois University, Carbondale, IL 62901, USA.
Brendan Clifford
Lacey Graybeal
Luke Tolley
Matthew E McCarroll

Funding

Design and evaluation of response selective fluorescent sensorsR15GM080721 · NIGMS · SOUTHERN ILLINOIS UNIVERSITY CARBONDALE · PI MCCARROLL, MATTHEW EVAN · 2008 to 2008
$217k
NIGMS NIH HHS R15 GM080721
6 · The paper itself

Abstract

Understanding molecular interactions is critical to understanding most biological mechanisms of cells and organisms. In the case of small molecule-protein interactions, many molecules have significant biological activity through interactions with unknown target proteins and by unknown modes of action. Identifying these target proteins is of significant importance and ongoing work in our laboratories is developing a technique termed Dynamic Isoelectric Anisotropy Binding Ligand Assay (DIABLA) to meet this need. Work presented in this manuscript aims to characterize the fundamental parameters affecting the use of fluorescence anisotropy to detect target proteins for a given ligand. Emphasis is placed on evaluating the use of fluorescence anisotropy as a detection mechanism, including optimization factors that affect the protein detection limit. Effects of ligand concentration, pH, and nonspecific binding are also examined.

Indexed as

BiotinCyclooxygenase 1Fluorescence PolarizationIbuprofenKineticsLigandsMolecular StructureNaproxenProgesteroneStreptavidinThermodynamicsBiotinCyclooxygenase 1IbuprofenLigandsNaproxenProgesteroneStreptavidin

Identifiers

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.