Evidence map›Paper›PMID 26118423›Full record

ArticleScientific reports2015

Fast, multi-frequency, and quantitative nanomechanical mapping of live cells using the atomic force microscope.

Alexander X Cartagena-Rivera, Wen-Horng Wang, Robert L Geahlen, Arvind Raman

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
10.1field-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, 116 citations in OpenAlex.

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  12. Cell wall dynamics: novel tools and research questions.Journal of experimental botany · 2023
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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

4 authors at 1 institution in 1 country.

Alexander X Cartagena-Rivera1] School of Mechanical Engineering, Purdue University, West Lafayette, Indiana, USA [2] Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana, USA.
Wen-Horng WangDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana, USA.
Robert L Geahlen1] Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana, USA [2] Purdue University Center for Cancer Research, Purdue University, West Lafayette, Indiana, USA.
Arvind Raman1] School of Mechanical Engineering, Purdue University, West Lafayette, Indiana, USA [2] Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana, USA.
Purdue University West Lafayette · US

Funding

Tyrosine Kinases and Lymphocyte ActivationR01AI098132 · NIAID · PURDUE UNIVERSITY · PI GEAHLEN, ROBERT L · 2012 to 2016
$1.6M
Syk and associated proteins in breast cancerR01CA115465 · NCI · PURDUE UNIVERSITY · PI GEAHLEN, ROBERT L · 2007 to 2011
$1.4M
NCI NIH HHS CA115465NCI NIH HHS R01 CA115465NIAID NIH HHS AI098132NIAID NIH HHS R01 AI098132
6 · The paper itself

Abstract

A longstanding goal in cellular mechanobiology has been to link dynamic biomolecular processes underpinning disease or morphogenesis to spatio-temporal changes in nanoscale mechanical properties such as viscoelasticity, surface tension, and adhesion. This requires the development of quantitative mechanical microscopy methods with high spatio-temporal resolution within a single cell. The Atomic Force Microscope (AFM) can map the heterogeneous mechanical properties of cells with high spatial resolution, however, the image acquisition time is 1-2 orders of magnitude longer than that required to study dynamic cellular processes. We present a technique that allows commercial AFM systems to map quantitatively the dynamically changing viscoelastic properties of live eukaryotic cells at widely separated frequencies over large areas (several 10's of microns) with spatial resolution equal to amplitude-modulation (AM-AFM) and with image acquisition times (tens of seconds) approaching those of speckle fluorescence methods. This represents a ~20 fold improvement in nanomechanical imaging throughput compared to AM-AFM and is fully compatible with emerging high speed AFM systems. This method is used to study the spatio-temporal mechanical response of MDA-MB-231 breast carcinoma cells to the inhibition of Syk protein tyrosine kinase giving insight into the signaling pathways by which Syk negatively regulates motility of highly invasive cancer cells.

Indexed as

Actin CytoskeletonAnimalsCell Line, TumorCell SurvivalElasticityFeedbackFibroblastsHumansImaging, Three-DimensionalIntracellular Signaling Peptides and ProteinsMicroscopy, Atomic ForceNanotechnologyProtein-Tyrosine KinasesRatsSpatio-Temporal AnalysisSyk KinaseIntracellular Signaling Peptides and ProteinsProtein-Tyrosine KinasesSyk KinaseSYK protein, humanSyk protein, rat

Identifiers

PMID26118423
PMCPMC4484408
OpenAlexW2255367475

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.