Evidence map›Paper›PMID 40334911›Full record

ArticleBiophysical reports2025

Image-based 3D active sample stabilization on the nanometer scale for optical microscopy.

Jakob Vorlaufer, Nikolai Semenov, Caroline Kreuzinger, Manjunath G Javoor, Bettina Zens, Nathalie Agudelo Dueñas, Mojtaba R Tavakoli, Marek Šuplata, Wiebke Jahr, Julia Lyudchik and 3 more

Abstract read
In one paragraph

Article in Biophysical reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Jakob VorlauferInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Nikolai SemenovInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Caroline KreuzingerInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Manjunath G JavoorInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Bettina ZensInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Nathalie Agudelo DueñasInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Mojtaba R TavakoliInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Marek ŠuplataInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Wiebke JahrInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Julia LyudchikInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Andreas WartakInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Florian K M SchurInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Johann G DanzlInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria. Electronic address: johann.danzl@ist.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Super-resolution microscopy often entails long acquisition times of minutes to hours. Since drifts during the acquisition adversely affect data quality, active sample stabilization is commonly used for some of these techniques to reach their full potential. Although drifts in the lateral plane can often be corrected after acquisition, this is not always possible or may come with drawbacks. Therefore, it is appealing to stabilize sample position in three dimensions (3D) during acquisition. Various schemes for active sample stabilization have been demonstrated previously, with some reaching sub-nanometer stability in 3D. Here, we present a scheme for active drift correction that delivers the nanometer-scale 3D stability demanded by state-of-the-art super-resolution techniques and is straightforward to implement compared to previous schemes capable of reaching this level of stabilization precision. Using a refined algorithm that can handle various types of reference structure, without sparse signal peaks being mandatory, we stabilized sample position to ∼1 nm in 3D using objective lenses both with high and low numerical aperture. Our implementation requires only the addition of a simple widefield imaging path and we provide an open-source control software with graphical user interface to facilitate easy adoption of the module. Finally, we demonstrate how this has the potential to enhance data collection for diffraction-limited and super-resolution imaging techniques using single-molecule localization microscopy and cryo-confocal imaging as showcases.

Indexed as

Imaging, Three-DimensionalMicroscopyAlgorithmsSoftware

Identifiers

PMID40334911
PMCPMC12166792

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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.