Evidence map›Paper›PMID 36362194›Full record

ArticleInternational journal of molecular sciences2022

Two-Photon Excitation Spectra of Various Fluorescent Proteins within a Broad Excitation Range.

Ruth Leben, Randall L Lindquist, Anja E Hauser, Raluca Niesner, Asylkhan Rakhymzhan

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

5 authors.

Ruth LebenBiophysical Analytics, Deutsches Rheuma-Forschungszentrum (DRFZ), 10117 Berlin, Germany.ORCID 0000-0001-8188-2890
Randall L LindquistImmune Dynamics and Intravital Microscopy, Deutsches Rheuma-Forschungszentrum (DRFZ), 10117 Berlin, Germany.
Anja E HauserImmune Dynamics and Intravital Microscopy, Deutsches Rheuma-Forschungszentrum (DRFZ), 10117 Berlin, Germany.ORCID 0000-0002-7725-9526
Raluca NiesnerBiophysical Analytics, Deutsches Rheuma-Forschungszentrum (DRFZ), 10117 Berlin, Germany.ORCID 0000-0001-8969-5432
Asylkhan RakhymzhanBiophysical Analytics, Deutsches Rheuma-Forschungszentrum (DRFZ), 10117 Berlin, Germany.

Funding

Deutsche Forschungsgemeinschaft SPP1937 (HA5354/8-2)Deutsche Forschungsgemeinschaft TRR130 (C01, P17), SFB1444 (P14)
6 · The paper itself

Abstract

Two-photon excitation fluorescence laser-scanning microscopy is the preferred method for studying dynamic processes in living organ models or even in living organisms. Thanks to near-infrared and infrared excitation, it is possible to penetrate deep into the tissue, reaching areas of interest relevant to life sciences and biomedicine. In those imaging experiments, two-photon excitation spectra are needed to select the optimal laser wavelength to excite as many fluorophores as possible simultaneously in the sample under consideration. The more fluorophores that can be excited, and the more cell populations that can be studied, the better access to their arrangement and interaction can be reached in complex systems such as immunological organs. However, for many fluorophores, the two-photon excitation properties are poorly predicted from the single-photon spectra and are not yet available, in the literature or databases. Here, we present the broad excitation range (760 nm to 1300 nm) of photon-flux-normalized two-photon spectra of several fluorescent proteins in their cellular environment. This includes the following fluorescent proteins spanning from the cyan to the infrared part of the spectrum: mCerulean3, mTurquoise2, mT-Sapphire, Clover, mKusabiraOrange2, mOrange2, LSS-mOrange, mRuby2, mBeRFP, mCardinal, iRFP670, NirFP, and iRFP720.

Indexed as

Fluorescent DyesPhotonsAluminum OxideLasersMicroscopy, FluorescenceAluminum OxideFluorescent Dyescells expressing fluorescent proteinsHEK-293T cells and murine splenocytestwo-photon excitation spectrumtwo-photon fluorescence laser-scanning microscopy

Identifiers

PMID36362194
PMCPMC9656010

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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.