Evidence map›Paper›PMID 32019978›Full record

ArticleScientific reports2020

Inferring quantity and qualities of superimposed reaction rates from single molecule survival time distributions.

Matthias Reisser, Johannes Hettich, Timo Kuhn, Achim P Popp, Andreas Große-Berkenbusch, J Christof M Gebhardt

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  14. Impact ofInternational journal of molecular sciences · 2022
    Review
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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

6 authors.

Matthias Reisser *Institute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Johannes Hettich *Institute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Timo KuhnInstitute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Achim P PoppInstitute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Andreas Große-BerkenbuschInstitute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
J Christof M GebhardtInstitute of Biophysics, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany. christof.gebhardt@uni-ulm.de.ORCID http://orcid.org/0000-0003-1900-600X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actions of molecular species, for example binding of transcription factors to chromatin, may comprise several superimposed reaction pathways. The number and the rate constants of such superimposed reactions can in principle be resolved by inverse Laplace transformation of the corresponding distribution of reaction lifetimes. However, current approaches to solve this transformation are challenged by photobleaching-prone fluorescence measurements of lifetime distributions. Here, we present a genuine rate identification method (GRID), which infers the quantity, rates and amplitudes of dissociation processes from fluorescence lifetime distributions using a dense grid of possible decay rates. In contrast to common multi-exponential analysis of lifetime distributions, GRID is able to distinguish between broad and narrow clusters of decay rates. We validate GRID by simulations and apply it to CDX2-chromatin interactions measured by live cell single molecule fluorescence microscopy. GRID reveals well-separated narrow decay rate clusters of CDX2, in part overlooked by multi-exponential analysis. We discuss the amplitudes of the decay rate spectrum in terms of frequency of observed events and occupation probability of reaction states. We further demonstrate that a narrow decay rate cluster is compatible with a common model of TF sliding on DNA.

Indexed as

AnimalsCDX2 Transcription FactorCell LineChromatinDNAFluorescenceKineticsMiceMicroscopy, FluorescenceNIH 3T3 CellsProbabilitySpectrometry, FluorescenceCDX2 Transcription FactorChromatinDNA

Identifiers

PMID32019978
PMCPMC7000831

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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.