Evidence map›Paper›PMID 32545175›Full record

ReviewInternational journal of molecular sciences2020

Back to the Future: Genetically Encoded Fluorescent Proteins as Inert Tracers of the Intracellular Environment.

Francesco Cardarelli

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Cytoplasmic crowding acts as a porous medium reducing macromolecule diffusion.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. 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

1 author.

Francesco CardarelliNEST - Scuola Normale Superiore, Istituto Nanoscienze - CNR (CNR-NANO), Piazza San Silvestro 12, 56127 Pisa, Italy.ORCID 0000-0003-3049-5940

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca 2017YF9FBS
6 · The paper itself

Abstract

Over the past decades, the discovery and development of genetically encoded fluorescent proteins (FPs) has brought a revolution into our ability to study biologic phenomena directly within living matter. First, FPs enabled fluorescence-labeling of a variety of molecules of interest to study their localization, interactions and dynamic behavior at various scales-from cells to whole organisms/animals. Then, rationally engineered FP-based sensors facilitated the measurement of physicochemical parameters of living matter-especially at the intracellular level, such as ion concentration, temperature, viscosity, pressure, etc. In addition, FPs were exploited as inert tracers of the intracellular environment in which they are expressed. This oft-neglected role is made possible by two distinctive features of FPs: (

Indexed as

AnimalsBiomarkersCell NucleusCytoplasmFluorescence Recovery After PhotobleachingFluorescence Resonance Energy TransferGreen Fluorescent ProteinsLuminescent ProteinsMolecular BiologyBiomarkersGreen Fluorescent ProteinsLuminescent ProteinscytoplasmdiffusionfluorescenceGFPinert tracernucleustime-resolved methods

Identifiers

PMID32545175
PMCPMC7312867

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.