Evidence map›Paper›PMID 25535361›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Stochastic approach to the molecular counting problem in superresolution microscopy.

Geoffrey C Rollins, Jae Yen Shin, Carlos Bustamante, Steve Pressé

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
14.1field-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

46 citing papers in PubMed, 118 citations in OpenAlex.

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  13. Quantifying molecular- to cellular-level forces in living cells.Journal of physics D: Applied physics · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Geoffrey C RollinsDepartment of Biochemistry and Biophysics, University of California, San Francisco, CA 94158;
Jae Yen ShinHoward Hughes Medical Institute and.
Carlos BustamanteHoward Hughes Medical Institute and Departments of Physics, Molecular and Cell Biology, and Chemistry, QB3 Institute, University of California, Berkeley, CA 94720;
Steve PresséDepartment of Physics, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202; and Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN 46202 stevenpresse@gmail.com.
Howard Hughes Medical Institute · USUniversity of California, San Francisco · USUniversity of Indianapolis · US

Funding

STRUCTURAL BIOLOGY TRAINING PROGRAMT32GM008284 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KORTEMME, TANJA · 1988 to 2022
$10.1M
THE PHYSICAL CHEMISTRY OF NUCLEIC ACIDSR01GM032543 · NIGMS · UNIVERSITY OF OREGON · PI CARLOS Jose BUSTAMANTE · 1985 to 2026
$6.4M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM032543NIGMS NIH HHS R01-GM032543
6 · The paper itself

Abstract

Superresolution imaging methods--now widely used to characterize biological structures below the diffraction limit--are poised to reveal in quantitative detail the stoichiometry of protein complexes in living cells. In practice, the photophysical properties of the fluorophores used as tags in superresolution methods have posed a severe theoretical challenge toward achieving this goal. Here we develop a stochastic approach to enumerate fluorophores in a diffraction-limited area measured by superresolution microscopy. The method is a generalization of aggregated Markov methods developed in the ion channel literature for studying gating dynamics. We show that the method accurately and precisely enumerates fluorophores in simulated data while simultaneously determining the kinetic rates that govern the stochastic photophysics of the fluorophores to improve the prediction's accuracy. This stochastic method overcomes several critical limitations of temporal thresholding methods.

Indexed as

Fluorescent DyesLikelihood FunctionsMacromolecular SubstancesMarkov ChainsMicroscopyMicroscopy, FluorescenceModels, ChemicalMolecular ImagingMultiprotein ComplexesPhotochemical ProcessesStochastic ProcessesFluorescent DyesMacromolecular SubstancesMultiprotein Complexescounting problemfluorescenceprotein complexessingle moleculesuperresolution

Identifiers

PMID25535361
PMCPMC4299210
OpenAlexW2122812646

What OpenQuestion holds

Textmetadata
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.