Evidence map›Paper›PMID 27196902›Full record

ArticleSensors (Basel, Switzerland)2016

Anchoring of FRET Sensors-A Requirement for Spatiotemporal Resolution.

Elena V Ivanova, Ricardo A Figueroa, Tom Gatsinzi, Einar Hallberg, Kerstin Iverfeldt

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  2. 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

5 authors.

Elena V IvanovaDepartment of Neurochemistry, Stockholm University, Svante Arrhenius väg. 16A, SE 10691 Stockholm, Sweden. elena.ivanova@neurochem.su.se.
Ricardo A FigueroaDepartment of Neurochemistry, Stockholm University, Svante Arrhenius väg. 16A, SE 10691 Stockholm, Sweden. ricardo@neurochem.su.se.
Tom GatsinziDepartment of Neurochemistry, Stockholm University, Svante Arrhenius väg. 16A, SE 10691 Stockholm, Sweden. tom.gatsinzi@gmail.com.
Einar HallbergDepartment of Neurochemistry, Stockholm University, Svante Arrhenius väg. 16A, SE 10691 Stockholm, Sweden. einar.hallberg@neurochem.su.se.
Kerstin IverfeldtDepartment of Neurochemistry, Stockholm University, Svante Arrhenius väg. 16A, SE 10691 Stockholm, Sweden. kerstin@neurochem.su.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FRET biosensors have become a routine tool for investigating mechanisms and components of cell signaling. Strategies for improving them for particular applications are continuously sought. One important aspect to consider when designing FRET probes is the dynamic distribution and propagation of signals within living cells. We have addressed this issue by directly comparing an anchored (taFS) to a non-anchored (naFS) cleavable FRET sensor. We chose a microtubule-associated protein tau as an anchor, as microtubules are abundant throughout the cytosol of cells. We show that tau-anchored FRET sensors are concentrated at the cytoskeleton and enriched in the neurite-like processes of cells, providing high intensity of the total signal. In addition, anchoring limits the diffusion of the sensor, enabling spatiotemporally resolved monitoring of subcellular variations in enzyme activity. Thus, anchoring is an important aspect to consider when designing FRET sensors for deeper understanding of cell signaling.

Indexed as

Biosensing TechniquesFluorescence Resonance Energy TransferMicrotubulesSignal TransductionapoptosiscaspaseFRET sensorlive cell imagingneurodegenerationsignal transduction

Identifiers

PMID27196902
PMCPMC4883394

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.