Evidence map›Paper›PMID 33778003›Full record

ArticleFrontiers in molecular biosciences2021

CUTie2: The Attack of the Cyclic Nucleotide Sensor Clones.

Florencia Klein, Florencia Sardi, Matías R Machado, Claudia Ortega, Marcelo A Comini, Sergio Pantano

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2021. 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
0.5field-weighted citation impact, top 39% 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, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. A FRET-based cGMP biosensor inmicroPublication biology · 2023
    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

6 authors at 2 institutions in 2 countries.

Florencia KleinBioMolecular Simulation Group, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Florencia SardiLaboratory Redox Biology of Trypanosomes, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Matías R MachadoBioMolecular Simulation Group, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Claudia OrtegaRecombinant Protein Unit, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Marcelo A CominiLaboratory Redox Biology of Trypanosomes, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Sergio PantanoBioMolecular Simulation Group, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Institut Pasteur de Montevideo · UYUniversidad de la República · UY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The detection of small molecules in living cells using genetically encoded FRET sensors has revolutionized our understanding of signaling pathways at the sub-cellular level. However, engineering fluorescent proteins and specific binding domains to create new sensors remains challenging because of the difficulties associated with the large size of the polypeptides involved, and their intrinsically huge conformational variability. Indeed, FRET sensors' design still relies on vague structural notions, and trial and error combinations of linkers and protein modules. We recently designed a FRET sensor for the second messenger cAMP named CUTie (

Indexed as

biosensorcoarse-grainedCUTiecyclic nucleotideFRETmolecular dynamicssignalingSirah

Identifiers

PMID33778003
PMCPMC7991088
OpenAlexW3135563769

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.