Evidence map›Paper›PMID 34848821›Full record

ArticleCommunications biology2021

Infrared nanoscopy and tomography of intracellular structures.

Katerina Kanevche, David J Burr, Dennis J Nürnberg, Pascal K Hass, Andreas Elsaesser, Joachim Heberle

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Nanosecond Transient IR Spectroscopy of Halorhodopsin in Living Cells.Journal of the American Chemical Society · 2024
    Article
  9. Article
  10. Visualization of Nanocarriers and Drugs in Cells and Tissue.Handbook of experimental pharmacology · 2024
    Article
  11. Molecular design and synthesis of methoxy-substitued spiropyrans with photomodulated NIR-fluorescence.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  12. Article
  13. Toward the Next Frontiers of Vibrational Bioimaging.Chemical & biomedical imaging · 2023
    Review
  14. 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

6 authors at 1 institution in 1 country.

Katerina KanevcheFreie Universität Berlin, Department of Physics, Experimental Molecular Biophysics, Arnimallee 14, 14195, Berlin, Germany.ORCID http://orcid.org/0000-0002-0651-3689
David J BurrFreie Universität Berlin, Department of Physics, Experimental Biophysics and Space Sciences, Arnimallee 14, 14195, Berlin, Germany.
Dennis J NürnbergFreie Universität Berlin, Department of Physics, Biochemistry and Biophysics of Photosynthetic Organisms, Arnimallee 14, 14195, Berlin, Germany.ORCID http://orcid.org/0000-0001-8644-3424
Pascal K HassFreie Universität Berlin, Department of Veterinary Medicine, Institute of Veterinary Anatomy Koserstr. 20, 14195, Berlin, Germany.
Andreas ElsaesserFreie Universität Berlin, Department of Physics, Experimental Biophysics and Space Sciences, Arnimallee 14, 14195, Berlin, Germany. a.elsaesser@fu-berlin.de.ORCID http://orcid.org/0000-0002-3781-8290
Joachim HeberleFreie Universität Berlin, Department of Physics, Experimental Molecular Biophysics, Arnimallee 14, 14195, Berlin, Germany. joachim.heberle@fu-berlin.de.ORCID http://orcid.org/0000-0001-6321-2615
Freie Universität Berlin · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) HE 2063/5-1
6 · The paper itself

Abstract

Although techniques such as fluorescence-based super-resolution imaging or confocal microscopy simultaneously gather both morphological and chemical data, these techniques often rely on the use of localized and chemically specific markers. To eliminate this flaw, we have developed a method of examining cellular cross sections using the imaging power of scattering-type scanning near-field optical microscopy and Fourier-transform infrared spectroscopy at a spatial resolution far beyond the diffraction limit. Herewith, nanoscale surface and volumetric chemical imaging is performed using the intrinsic contrast generated by the characteristic absorption of mid-infrared radiation by the covalent bonds. We employ infrared nanoscopy to study the subcellular structures of eukaryotic (Chlamydomonas reinhardtii) and prokaryotic (Escherichia coli) species, revealing chemically distinct regions within each cell such as the microtubular structure of the flagellum. Serial 100 nm-thick cellular cross-sections were compiled into a tomogram yielding a three-dimensional infrared image of subcellular structure distribution at 20 nm resolution. The presented methodology is able to image biological samples complementing current fluorescence nanoscopy but at less interference due to the low energy of infrared radiation and the absence of labeling.

Indexed as

Chlamydomonas reinhardtiiEscherichia coliMicroscopySpectrophotometry, InfraredSpectroscopy, Fourier Transform Infrared

Identifiers

PMID34848821
PMCPMC8633277
OpenAlexW3183499876

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.