Evidence map›Paper›PMID 37278763›Full record

ArticleThe Journal of cell biology2023

Development of ultrafast camera-based single fluorescent-molecule imaging for cell biology.

Takahiro K Fujiwara, Shinji Takeuchi, Ziya Kalay, Yosuke Nagai, Taka A Tsunoyama, Thomas Kalkbrenner, Kokoro Iwasawa, Ken P Ritchie, Kenichi G N Suzuki, Akihiro Kusumi

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
16.4field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

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  8. High-Speed Interferometric Scattering Tracking Microscopy of Compartmentalized Lipid Diffusion in Living Cells.Chemphyschem : a European journal of chemical physics and physical chemistry · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Takahiro K FujiwaraInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University , Kyoto, Japan.ORCID 0000-0001-5576-759X
Shinji TakeuchiPhotron Limited , Tokyo, Japan.ORCID 0009-0005-7666-3649
Ziya KalayInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University , Kyoto, Japan.ORCID 0000-0003-4103-1623
Yosuke NagaiPhotron Limited , Tokyo, Japan.ORCID 0009-0009-5388-2581
Taka A TsunoyamaMembrane Cooperativity Unit, Okinawa Institute of Science and Technology Graduate University (OIST) , Okinawa, Japan.ORCID 0000-0003-1457-7612
Thomas KalkbrennerCarl Zeiss Microscopy GmbH , Jena, Germany.ORCID 0009-0002-6903-7947
Kokoro IwasawaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University , Kyoto, Japan.ORCID 0009-0003-5961-0380
Ken P RitchieDepartment of Physics and Astronomy, Purdue University , West Lafayette, IN, USA.ORCID 0000-0002-8445-6042
Kenichi G N SuzukiInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University , Kyoto, Japan.ORCID 0000-0002-8436-5757
Akihiro KusumiInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University , Kyoto, Japan.ORCID 0000-0002-9558-6950
Kyoto University · JPOkinawa Institute of Science and Technology Graduate University · JPCarl Zeiss (Germany) · DEPurdue University West Lafayette · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spatial resolution of fluorescence microscopy has recently been greatly enhanced. However, improvements in temporal resolution have been limited, despite their importance for examining living cells. Here, we developed an ultrafast camera system that enables the highest time resolutions in single fluorescent-molecule imaging to date, which were photon-limited by fluorophore photophysics: 33 and 100 µs with single-molecule localization precisions of 34 and 20 nm, respectively, for Cy3, the optimal fluorophore we identified. Using theoretical frameworks developed for the analysis of single-molecule trajectories in the plasma membrane (PM), this camera successfully detected fast hop diffusion of membrane molecules in the PM, previously detectable only in the apical PM using less preferable 40-nm gold probes, thus helping to elucidate the principles governing the PM organization and molecular dynamics. Furthermore, as described in the companion paper, this camera allows simultaneous data acquisitions for PALM/dSTORM at as fast as 1 kHz, with 29/19 nm localization precisions in the 640 × 640 pixel view-field.

Indexed as

Fluorescent DyesNanotechnologyCell BiologyCell MembraneDiffusionMicroscopy, FluorescenceSingle Molecule ImagingFluorescent Dyes

Identifiers

PMID37278763
PMCPMC10244617
OpenAlexW4379508609

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.