Evidence map›Paper›PMID 26404317›Full record

ArticleSensors (Basel, Switzerland)2015

FRET-Based Nanobiosensors for Imaging Intracellular Ca²⁺ and H⁺ Microdomains.

Alsu I Zamaleeva, Guillaume Despras, Camilla Luccardini, Mayeul Collot, Michel de Waard, Martin Oheim, Jean-Maurice Mallet, Anne Feltz

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2015. 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
–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

3 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Alsu I ZamaleevaEcole Normale Supérieure, Institut de Biologie de l'ENS (IBENS), Inserm U1024, CNRS UMR 8197, Paris F-75005, France. alsu.zamaleeva@curie.fr.
Guillaume DesprasDepartment de Chimie, École Normale Supérieure-PSL Research University, CNRS UMR 7203 LBM, 24, rue Lhomond, and Sorbonne University, UPMC Univ Paris 06 LBM, 4 place Jussieu, Paris F-75005, France. gdespras@oc.uni-kiel.de.
Camilla LuccardiniEcole Normale Supérieure, Institut de Biologie de l'ENS (IBENS), Inserm U1024, CNRS UMR 8197, Paris F-75005, France. Camilla.luccardini@univ-lyon1.fr.
Mayeul CollotDepartment de Chimie, École Normale Supérieure-PSL Research University, CNRS UMR 7203 LBM, 24, rue Lhomond, and Sorbonne University, UPMC Univ Paris 06 LBM, 4 place Jussieu, Paris F-75005, France. mayeul.collot@unistra.fr.
Michel de WaardInserm U836, Grenoble Neuroscience Institute, Research Group 3, LabEx Ion Channel Science and Therapeutics, Joseph Fourier University, BP170, Grenoble Cedex 09 38042, France. Michel.dewaard@ujf-grenoble.fr.
Martin OheimBrain Physiology Laboratory, CNRS UMR 8118, Faculté des Sciences Fondamentales et Biomédicales, Fédération de Neurosciences FR3636, Paris Descartes University, PRES Sorbonne Paris Cité, Paris F-75006, France. Martin.oheim@parisdescartes.fr.
Jean-Maurice MalletDepartment de Chimie, École Normale Supérieure-PSL Research University, CNRS UMR 7203 LBM, 24, rue Lhomond, and Sorbonne University, UPMC Univ Paris 06 LBM, 4 place Jussieu, Paris F-75005, France. jean-maurice.mallet@ens.fr.
Anne FeltzEcole Normale Supérieure, Institut de Biologie de l'ENS (IBENS), Inserm U1024, CNRS UMR 8197, Paris F-75005, France. anne.feltz@ens.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semiconductor nanocrystals (NCs) or quantum dots (QDs) are luminous point emitters increasingly being used to tag and track biomolecules in biological/biomedical imaging. However, their intracellular use as highlighters of single-molecule localization and nanobiosensors reporting ion microdomains changes has remained a major challenge. Here, we report the design, generation and validation of FRET-based nanobiosensors for detection of intracellular Ca(2+) and H⁺ transients. Our sensors combine a commercially available CANdot(®)565QD as an energy donor with, as an acceptor, our custom-synthesized red-emitting Ca(2+) or H⁺ probes. These 'Rubies' are based on an extended rhodamine as a fluorophore and a phenol or BAPTA (1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetra-acetic acid) for H⁺ or Ca(2+) sensing, respectively, and additionally bear a linker arm for conjugation. QDs were stably functionalized using the same SH/maleimide crosslink chemistry for all desired reactants. Mixing ion sensor and cell-penetrating peptides (that facilitate cytoplasmic delivery) at the desired stoichiometric ratio produced controlled multi-conjugated assemblies. Multiple acceptors on the same central donor allow up-concentrating the ion sensor on the QD surface to concentrations higher than those that could be achieved in free solution, increasing FRET efficiency and improving the signal. We validate these nanosensors for the detection of intracellular Ca(2+) and pH transients using live-cell fluorescence imaging.

Indexed as

ProtonsAnimalsBiophysical PhenomenaBiosensing TechniquesCalciumCell LineEndocytosisEndosomesFluorescence Resonance Energy TransferFluorescent DyesIntracellular SpaceIonsLysosomesMolecular ImagingNanoparticlesQuantum DotsCalciumFluorescent DyesIonsProtonsRhodaminescell-penetrating peptideconcentration microdomainFRET-based Ca2+ and H+ probesintracellular Ca2+ and H+ fluorometrynanoparticle surface chemistryquantum dot nanobiosensorsred-emitting indicator

Identifiers

PMID26404317
PMCPMC4610457

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Registered trials

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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.