Evidence map›Paper›PMID 20836709›Full record

ArticleAssay and drug development technologies2011

Bioluminescence assay for detecting cell surface membrane protein expression.

Mieko Kato, Tomoki Chiba, Min Li, Yoshiro Hanyu

Open access · greenAbstract read
In one paragraph

Article in Assay and drug development technologies, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Review
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

4 authors at 3 institutions in 2 countries.

Mieko KatoSignaling Molecules Research Group, Neuroscience Research Institute, National Institutes of Advanced Industrial Science and Technology, Tsukuba, 1-1-1 Higashi, Tsukuba, Japan.
Tomoki Chiba
Min Li
Yoshiro Hanyu
University of Tsukuba · JPJohns Hopkins University · USNational Institute of Advanced Industrial Science and Technology · JP

Funding

Johns Hopkins Ion Channel CenterU54MH084691 · NIMH · JOHNS HOPKINS UNIVERSITY · PI LI, MIN · 2008 to 2012
$13.9M
Molecular regulation of calcium-activated (BK) potassium channelsR01GM078579 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LI, MIN · 2007 to 2010
$1.2M
NIGMS NIH HHS GM078579NIMH NIH HHS MH084691
6 · The paper itself

Abstract

We have developed a method to measure the amounts of cell surface-expressed membrane proteins with bioluminescence. Dinoflagellate luciferase was expressed on the surface of a mammalian cell as a chimeric fusion protein with a membrane protein of interest. Using a membrane-impermeable substrate to quantify the membrane-displayed luciferase, the expression of the membrane protein on the cell surface was determined. By inclusion of a quenching step for the luminescent activity of luciferase on the cell surface, we were able to monitor the membrane protein expression kinetics by measuring the luminescence recovery from the cell surface after quenching. The reported methods provide a convenient way to monitor the kinetics of expression and transport of membrane proteins to the cell surface. It is applicable to the high-throughput analysis of drugs or drug candidates concerning their effects on membrane protein expression.

Indexed as

Biological AssayCell MembraneGene Expression ProfilingHumansLuciferasesLuminescent MeasurementsLuminescent ProteinsMembrane ProteinsLuciferasesLuminescent ProteinsMembrane Proteins

Identifiers

PMID20836709
PMCPMC3064531
OpenAlexW1971484663

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.