Evidence map›Paper›PMID 29091397›Full record

ArticleACS nano2017

Nanoscale Properties of Human Telomeres Measured with a Dual Purpose X-ray Fluorescence and Super Resolution Microscopy Gold Nanoparticle Probe.

J Charles G Jeynes, Kalotina Geraki, Christopher Jeynes, Mi Zhaohong, Andrew A Bettiol, Eva Latorre, Lorna Wendy Harries, Christian Soeller

Open access · hybridAbstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Taming Mre11-Rad50 at Telomeres: Convergent Strategies for Chromosome-End Protection Across Evolution.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
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  12. Role of mismatch repair in aging.International journal of biological sciences · 2021
    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

8 authors at 4 institutions in 2 countries.

J Charles G JeynesCentre for Biomedical Modelling and Analysis, University of Exeter , Exeter, Devon, U.K. , EX2 5DW.ORCID 0000-0002-4354-3852
Kalotina GerakiDiamond Light Source , Didcot, Oxfordshire U.K. , OX11 0DE.
Christopher JeynesIon Beam Centre, University of Surrey , Guildford, Surrey, U.K. , GU2 7XH.
Mi ZhaohongCentre for Ion Beam Applications, National University of Singapore , Singapore , 119077.
Andrew A BettiolCentre for Ion Beam Applications, National University of Singapore , Singapore , 119077.ORCID 0000-0001-5242-3644
Eva LatorreMedical School, RILD Building, University of Exeter , Barrack Road, Exeter, Devon, EX2 5DW.
Lorna Wendy HarriesMedical School, RILD Building, University of Exeter , Barrack Road, Exeter, Devon, EX2 5DW.
Christian SoellerLiving Systems Institute & Biomedical Physics, University of Exeter , Exeter, Devon, U.K. , EX2 5DW.
University of Exeter · GBNational University of Singapore · SGDiamond Light Source · GBUniversity of Surrey · GB

Funding

Wellcome TrustWellcome Trust WT105618MA
6 · The paper itself

Abstract

Techniques to analyze human telomeres are imperative in studying the molecular mechanism of aging and related diseases. Two important aspects of telomeres are their length in DNA base pairs (bps) and their biophysical nanometer dimensions. However, there are currently no techniques that can simultaneously measure these quantities in individual cell nuclei. Here, we develop and evaluate a telomere "dual" gold nanoparticle-fluorescent probe simultaneously compatible with both X-ray fluorescence (XRF) and super resolution microscopy. We used silver enhancement to independently visualize the spatial locations of gold nanoparticles inside the nuclei, comparing to a standard QFISH (quantitative fluorescence in situ hybridization) probe, and showed good specificity at ∼90%. For sensitivity, we calculated telomere length based on a DNA/gold binding ratio using XRF and compared to quantitative polymerase chain reaction (qPCR) measurements. The sensitivity was low (∼10%), probably because of steric interference prohibiting the relatively large 10 nm gold nanoparticles access to DNA space. We then measured the biophysical characteristics of individual telomeres using super resolution microscopy. Telomeres that have an average length of ∼10 kbps, have diameters ranging between ∼60-300 nm. Further, we treated cells with a telomere-shortening drug and showed there was a small but significant difference in telomere diameter in drug-treated vs control cells. We discuss our results in relation to the current debate surrounding telomere compaction.

Indexed as

FluorescenceCells, CulturedFluorescent DyesGoldHEK293 CellsHumansMetal NanoparticlesMicroscopy, FluorescenceOptical ImagingTelomereX-RaysFluorescent DyesGolddSTORMnanoparticlessuper resolution microscopytelomeresX-ray fluorescence

Identifiers

PMID29091397
PMCPMC5951601
OpenAlexW2766023415

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.