Evidence map›Paper›PMID 10620311›Full record

ArticleBiophysical journal2000

Resolving heterogeneity on the single molecular level with the photon-counting histogram.

J D Müller, Y Chen, E Gratton

Abstract read
In one paragraph

Article in Biophysical journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing 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

68 citing papers in PubMed.

  1. Article
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  11. BetaBiochimica et biophysica acta. Biomembranes · 2017
    Article
  12. Article
  13. Article
  14. Correlation of focal adhesion assembly and disassembly with cell migration on nanotopography.Integrative biology : quantitative biosciences from nano to macro · 2017
    Article
  15. Article
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  19. Article
  20. H-Ras forms dimers on membrane surfaces via a protein-protein interface.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article

8 more citing papers are in PubMed but not listed here.

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

3 authors.

J D MüllerLaboratory for Fluorescence Dynamics, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801 USA. muller@uiuc.edu
Y Chen
E Gratton

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diffusion of fluorescent particles through a small, illuminated observation volume gives rise to intensity fluctuations caused by particle number fluctuations in the open observation volume and the inhomogeneous excitation-beam profile. The intensity distribution of these fluorescence fluctuations is experimentally captured by the photon-counting histogram (PCH). We recently introduced the theory of the PCH for diffusing particles (Chen et al., Biophys. J., 77:553-567), where we showed that we can uniquely describe the distribution of photon counts with only two parameters for each species: the molecular brightness of the particle and the average number of particles within the observation volume. The PCH is sensitive to the molecular brightness and thus offers the possibility to separate a mixture of fluorescent species into its constituents, based on a difference in their molecular brightness alone. This analysis is complementary to the autocorrelation function, traditionally used in fluorescence fluctuation spectroscopy, which separates a mixture of species by a difference in their diffusion coefficient. The PCH of each individual species is convoluted successively to yield the PCH of the mixture. Successful resolution of the histogram into its components is largely a matter of the signal statistics. Here, we discuss the case of two species in detail and show that a concentration for each species exists, where the signal statistics is optimal. We also discuss the influence of the absolute molecular brightness and the brightness contrast between two species on the resolvability of two species. A binary dye mixture serves as a model system to demonstrate that the molecular brightness and the concentration of each species can be resolved experimentally from a single or from several histograms. We extend our study to biomolecules, where we label proteins with a fluorescent dye and show that a brightness ratio of two can be resolved. The ability to resolve a brightness ratio of two is very important for biological applications.

Indexed as

Fluorescent DyesPhotonsAlcohol DehydrogenaseMicroscopy, FluorescenceModels, TheoreticalAlcohol DehydrogenaseFluorescent Dyes

Identifiers

PMID10620311
PMCPMC1300655

What OpenQuestion holds

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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.