Evidence map›Paper›PMID 20572284›Full record

ArticleJournal of biophotonics2010

Ultrasensitive label-free photothermal imaging, spectral identification, and quantification of cytochrome c in mitochondria, live cells, and solutions.

Anton V Brusnichkin, Dmitry A Nedosekin, Ekaterina I Galanzha, Yuri A Vladimirov, Elena F Shevtsova, Mikhail A Proskurnin, Vladimir P Zharov

Abstract readEvaluation Study
In one paragraph

Article in Journal of biophotonics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Composition of the CytochromeMolecules (Basel, Switzerland) · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Label-free photoacoustic nanoscopy.Journal of biomedical optics · 2014
    Article
  11. Article
  12. Article
  13. Label-free photoacoustic microscopy of cytochromes.Journal of biomedical optics · 2013
    Article
  14. Article
  15. In vivo photoacoustic and photothermal cytometry for monitoring multiple blood rheology parameters.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2011
    Review
  16. 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

7 authors.

Anton V BrusnichkinChemistry Department, M. V. Lomonosov Moscow State University, Vorob'evy Hills 1/3, Moscow 119991, Russia.
Dmitry A Nedosekin
Ekaterina I Galanzha
Yuri A Vladimirov
Elena F Shevtsova
Mikhail A Proskurnin
Vladimir P Zharov

Funding

In vivo real-time detection of circulating melanoma cellsR01CA131164 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI SUEN, JAMES · 2009 to 2019
$3.1M
Multifunctional nanotubes for in vivo detecting/purging circulating cancer cellsR01EB009230 · NIBIB · UNIV OF ARKANSAS FOR MED SCIS · PI ZHAROV, VLADIMIR P · 2009 to 2012
$1.2M
Photothermal Imaging of Live CellsR01EB000873 · NIBIB · UNIV OF ARKANSAS FOR MED SCIS · PI ZHAROV, VLADIMIR P · 2005 to 2008
$1.1M
In vivo molecular laser detection and treatment of circulating cancer stem cellsR21CA139373 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI ZHAROV, VLADIMIR P · 2009 to 2010
$329k
NCI NIH HHS R01 CA131164NCI NIH HHS R01CA131164NCI NIH HHS R21 CA139373NCI NIH HHS R21CA139373NIBIB NIH HHS R01 EB000873NIBIB NIH HHS R01EB000873NIBIB NIH HHS R01 EB009230
6 · The paper itself

Abstract

Light-absorbing endogenous cellular proteins, in particular cytochrome c, are used as intrinsic biomarkers for studies of cell biology and environment impacts. To sense cytochrome c against real biological backgrounds, we combined photothermal (PT) thermal-lens single-channel schematic in a back-synchronized measurement mode and a multiplex thermal-lens schematic in a transient high resolution (ca. 350 nm) imaging mode. These multifunctional PT techniques using continuous-wave (cw) Ar+ laser and a nanosecond pulsed optical parametric oscillator in the visible range demonstrated the capability for label-free spectral identification and quantification of trace amounts of cytochrome c in a single mitochondrion alone or within a single live cell. PT imaging data were verified in parallel by molecular targeting and fluorescent imaging of cellular cytochrome c. The detection limit of cytochrome c in a cw mode was 5 x 10(-9) mol/L (80 attomols in the signal-generation zone); that is ca. 10³ lower than conventional absorption spectroscopy. Pulsed fast PT microscopy provided the detection limit for cytochrome c at the level of 13 zmol (13 x 10(-21) mol) in the ultrasmall irradiated volumes limited by optical diffraction effects. For the first time, we demonstrate a combination of high resolution PT imaging with PT spectral identification and ultrasensitive quantitative PT characterization of cytochrome c within individual mitochondria in single live cells. A potential of far-field PT microscopy to sub-zeptomol detection thresholds, resolution beyond diffraction limit, PT Raman spectroscopy, and 3D imaging are further highlighted.

Indexed as

Cytochromes cDiagnostic ImagingHumansKB CellsMicroscopy, FluorescenceMitochondriaPhotometrySensitivity and SpecificitySpectrum AnalysisCytochromes c

Identifiers

PMID20572284
PMCPMC3350104

What OpenQuestion holds

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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.