Evidence map›Paper›PMID 42547289›Full record

ArticleJournal of molecular recognition : JMR2026

Prediction-Based Algorithms for Long-Range High-Speed Force Spectroscopy.

Lorenzo Villanueva, Yogesh Saravanan, Mar Eroles, Antoine Couderc, Jorge Rodriguez-Ramos, Qingze Zou, Felix Rico

Abstract read
In one paragraph

Article in Journal of molecular recognition : JMR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

7 authors.

Lorenzo VillanuevaAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0000-0003-0158-9980
Yogesh SaravananAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0009-0004-8690-818X
Mar ErolesAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0000-0003-3571-0769
Antoine CoudercAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0009-0001-8900-3608
Jorge Rodriguez-RamosAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0000-0001-9837-6257
Qingze ZouAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0000-0001-5183-4409
Felix RicoAix-Marseille Univ, INSERM, DyNaMo, Turing Centre for Living Systems, Marseille, France.ORCID https://orcid.org/0000-0002-7757-8340

Funding

Agence Nationale de la Recherche ANR-10-INBS-0004European Research Council (ERC) under the European Union's Horizon 2020 101189381European Research Council (ERC) under the European Union's Horizon 2020 772257French Agence Nationale de la Recherche ANR-23-CE30-0048National Science Foundation NSF-PFI-2234449National Science Foundation NSF-PHY-2412551Rutgers TechAdvance
6 · The paper itself

Abstract

We present a high-speed force microscopy platform mounted on a confocal microscope with a z sample stage enabling long-range, high-speed force spectroscopy measurements on biological samples. The control software is built on a field-programmable gate array (FPGA)-based data acquisition and processing system, complemented with a custom graphical user insterface (GUI). We introduce smart algorithms based on probe-engagement prediction algorithms that leverage previously measured probe-sample contact to accelerate the probe engagement to mm/s and decelerate it in proximity of contact to user-defined μm/s velocities. This significantly reduces long-range force curve acquisition time and data density. Using this system, we provide proof-of-concept mechanical maps of cell clusters to extract topography and viscoelastic parameters. To further explore the versatility of our system, we probed the forces required to extract membrane tethers from monocytic cells using ultrashort cantilevers functionalised with adhesion molecules. Our system allowed us to cover retract velocities from ~1 μm/s up to ~6000 μm/s, and to explore the dynamics of tether formation at physiologically relevant velocities. Our results show that coupling extended z displacement with the prediction-based engagement algorithms enables rapid, quantitative mechanical mapping of heterogeneous biological samples with large topography variation and supports measurements requiring long distances at high velocities.

Indexed as

AlgorithmsMicroscopy, Atomic ForceSpectrum AnalysisHumansMicroscopy, ConfocalPrediction AlgorithmsSoftwareforce spectroscopyhigh‐speed atomic force microscopylong‐range interactionsprediction‐based controlreal‐time algorithms

Identifiers

PMID42547289
PMCPMC13433138

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.