Evidence map›Paper›PMID 35417173›Full record

ArticleThe journal of physical chemistry. B2022

Imaging Fluorescence Blinking of a Mitochondrial Localization Probe: Cellular Localization Probes Turned into Multifunctional Sensors.

Zhixue Du, Joachim Piguet, Glib Baryshnikov, Johan Tornmalm, Baris Demirbay, Hans Ågren, Jerker Widengren

Open access · hybridAbstract read
In one paragraph

Article in The journal of physical chemistry. B, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 12 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

7 authors at 3 institutions in 1 country.

Zhixue DuRoyal Institute of Technology (KTH), Experimental Biomolecular Physics, Department Applied Physics, Albanova Univ Center, 106 91 Stockholm, Sweden.
Joachim PiguetRoyal Institute of Technology (KTH), Experimental Biomolecular Physics, Department Applied Physics, Albanova Univ Center, 106 91 Stockholm, Sweden.ORCID 0000-0002-4762-4887
Glib BaryshnikovLaboratory of Organic Electronics, Department of Science and Technology, Linköping University, SE-60174 Norrköping, Sweden.
Johan TornmalmRoyal Institute of Technology (KTH), Experimental Biomolecular Physics, Department Applied Physics, Albanova Univ Center, 106 91 Stockholm, Sweden.
Baris DemirbayRoyal Institute of Technology (KTH), Experimental Biomolecular Physics, Department Applied Physics, Albanova Univ Center, 106 91 Stockholm, Sweden.
Hans ÅgrenDepartment of Physics and Astronomy, Uppsala University, P.O. Box 516, SE-751 20 Uppsala, Sweden.ORCID 0000-0002-1763-9383
Jerker WidengrenRoyal Institute of Technology (KTH), Experimental Biomolecular Physics, Department Applied Physics, Albanova Univ Center, 106 91 Stockholm, Sweden.ORCID 0000-0003-3200-0374
KTH Royal Institute of Technology · SELinköping University · SEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial membranes and their microenvironments directly influence and reflect cellular metabolic states but are difficult to probe on site in live cells. Here, we demonstrate a strategy, showing how the widely used mitochondrial membrane localization fluorophore 10-nonyl acridine orange (NAO) can be transformed into a multifunctional probe of membrane microenvironments by monitoring its blinking kinetics. By transient state (TRAST) studies of NAO in small unilamellar vesicles (SUVs), together with computational simulations, we found that NAO exhibits prominent reversible singlet-triplet state transitions and can act as a light-induced Lewis acid forming a red-emissive doublet radical. The resulting blinking kinetics are highly environment-sensitive, specifically reflecting local membrane oxygen concentrations, redox conditions, membrane charge, fluidity, and lipid compositions. Here, not only cardiolipin concentration but also the cardiolipin acyl chain composition was found to strongly influence the NAO blinking kinetics. The blinking kinetics also reflect hydroxyl ion-dependent transitions to and from the fluorophore doublet radical, closely coupled to the proton-transfer events in the membranes, local pH, and two- and three-dimensional buffering properties on and above the membranes. Following the SUV studies, we show by TRAST imaging that the fluorescence blinking properties of NAO can be imaged in live cells in a spatially resolved manner. Generally, the demonstrated blinking imaging strategy can transform existing fluorophore markers into multiparametric sensors reflecting conditions of large biological relevance, which are difficult to retrieve by other means. This opens additional possibilities for fundamental membrane studies in lipid vesicles and live cells.

Indexed as

BlinkingCardiolipinsFluorescenceFluorescent DyesKineticsCardiolipinsFluorescent Dyes

Identifiers

PMID35417173
PMCPMC9059120
OpenAlexW4223925042

What OpenQuestion holds

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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.