Evidence map›Paper›PMID 24421317›Full record

ArticleThe Journal of biological chemistry2014

Photocleavable dimerizer for the rapid reversal of molecular trap antagonists.

Shubbir Ahmed, Jun Xie, David Horne, John C Williams

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. FKBP Ligands-Where We Are and Where to Go?Frontiers in pharmacology · 2018
    Review
  3. Article
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 2 institutions in 1 country.

Shubbir AhmedFrom the Department of Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California 91010.
Jun Xie
David Horne
John C Williams
Beckman Research InstituteCity of Hope · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Development of chemical induced molecular traps for time resolved, in vivo studieR21NS071166 · NINDS · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WILLIAMS, JOHN CHARLES · 2010 to 2011
$452k
NCI NIH HHS P30 CA033572NINDS NIH HHS R21 NS071166NINDS NIH HHS R21NS071166
6 · The paper itself

Abstract

Herein, we report the development of a photocleavable analog of AP20187, a cell-permeable molecule used to dimerize FK506-binding protein (FKBP) fusion proteins and initiate biological signaling cascades and gene expression or disrupt protein-protein interactions. We demonstrate that this reagent permits the unique ability to rapidly and specifically antagonize a molecular interaction in vitro and follow a biological process due to this acute antagonism (e.g. endosome dispersion) and to release the trap upon photocleavage to follow the cell's return to homeostasis. In addition, this photocleavable AP20187 analog can be used in other systems where the dimerization of FKBP has been used to initiate signaling pathways, offering the ability to correlate the duration of a signaling event and a cellular response.

Indexed as

Ultraviolet RaysAnimalsChlorocebus aethiopsCOS CellsElectrophoresis, Polyacrylamide GelEndosomesProtein MultimerizationRecombinant Fusion ProteinsTacrolimusTacrolimus Binding ProteinsAP20187Recombinant Fusion ProteinsTacrolimusTacrolimus Binding ProteinsDyneinEndosomesMicroscopyMicrotubulesMolecular TrapOrganellePhotocleavable AntagonistSignaling

Identifiers

PMID24421317
PMCPMC3931014
OpenAlexW1993133874

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.