Evidence map›Paper›PMID 36304321›Full record

ReviewFrontiers in bioinformatics2022

Multi-Dimensional Spectral Single Molecule Localization Microscopy.

Corey Butler, G Ezequiel Saraceno, Adel Kechkar, Nathan Bénac, Vincent Studer, Julien P Dupuis, Laurent Groc, Rémi Galland, Jean-Baptiste Sibarita

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
10.0field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Corey ButlerUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
G Ezequiel SaracenoUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Adel KechkarEcole Nationale Supérieure de Biotechnologie, Laboratoire de Bioengineering, Constantine, El Khroub, Algeria.
Nathan BénacUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Vincent StuderUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Julien P DupuisUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Laurent GrocUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Rémi GallandUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Jean-Baptiste SibaritaUniv. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297F-33000, F-33000, Bordeaux, France.
Institut Interdisciplinaire de Neuroscience · FRCentre National de la Recherche Scientifique · FRÉcole Normale Supérieure de Constantine · DZUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single molecule localization (SML) and tracking (SPT) techniques, such as (spt)PALM, (u/DNA)PAINT and quantum dot tracking, have given unprecedented insight into the nanoscale molecular organization and dynamics in living cells. They allow monitoring individual proteins with millisecond temporal resolution and high spatial resolution (<30 nm) by precisely localizing the point spread function (PSF) of individual emitters and tracking their position over time. While SPT methods have been extended to study the temporal dynamics and co-organization of multiple proteins, conventional experimental setups are restricted in the number of proteins they can probe simultaneously and usually have to tradeoff between the number of colors, the spatio-temporal resolution, and the field of view. Yet, localizing and tracking several proteins simultaneously at high spatial and temporal resolution within large field of views can provide important biological insights. By employing a dual-objective spectral imaging configuration compatible with live cell imaging combined with dedicated computation tools, we demonstrate simultaneous 3D single particle localization and tracking of multiple distinct species over large field of views to be feasible without compromising spatio-temporal resolution. The dispersive element introduced into the second optical path induces a spectrally dependent displacement, which we used to analytically separate up to five different fluorescent species of single emitters based on their emission spectra. We used commercially available microscope bodies aligned one on top of the other, offering biologists with a very ergonomic and flexible instrument covering a broad range of SMLM applications. Finally, we developed a powerful freely available software, called PALMTracer, which allows to quantitatively assess 3D + t + λ SMLM data. We illustrate the capacity of our approach by performing multi-color 3D DNA-PAINT of fixed samples, and demonstrate simultaneous tracking of multiple receptors in live fibroblast and neuron cultures.

Indexed as

live cell imagingmulti-emitter fittingsingle molecule localizationsingle particle trackingspectral imaging

Identifiers

PMID36304321
PMCPMC9580959
OpenAlexW4214909552

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.