Evidence map›Paper›PMID 25522343›Full record

ArticleMagnetic resonance in medicine2015

Engineering an effective Mn-binding MRI reporter protein by subcellular targeting.

Benjamin B Bartelle, Miyeko D Mana, Giselle A Suero-Abreu, Joe J Rodriguez, Daniel H Turnbull

Abstract read
In one paragraph

Article in Magnetic resonance in medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Cell Tracking in Cancer Immunotherapy.Frontiers in medicine · 2020
    Review
  9. Review
  10. Biomolecular MRI reporters: Evolution of new mechanisms.Progress in nuclear magnetic resonance spectroscopy · 2017
    Review
  11. NMR Hyperpolarization Techniques of Gases.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Development of Timd2 as a reporter gene for MRI.Magnetic resonance in medicine · 2016
    Article
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

5 authors.

Benjamin B BartelleSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.
Miyeko D ManaSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.
Giselle A Suero-AbreuSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.
Joe J RodriguezSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.
Daniel H TurnbullSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Ultrasound and MR Imaging of Mouse Brain Development.R01NS038461 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TURNBULL, DANIEL H · 1999 to 2016
$6.5M
Training program in Molecular BiophysicsT32GM088118 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI STOKES, DAVID L. · 2010 to 2019
$1.8M
NCI NIH HHS P30 CA016087NCI NIH HHS P30CA016087NIGMS NIH HHS T32 GM088118NINDS NIH HHS R01 NS038461NINDS NIH HHS R01NS038461
6 · The paper itself

Abstract

purposeManganese (Mn) is an effective contrast agent and biologically active metal, which has been widely used for Mn-enhanced MRI (MEMRI). The purpose of this study was to develop and test a Mn binding protein for use as a genetic reporter for MEMRI.

methodsThe bacterial Mn-binding protein, MntR was identified as a candidate reporter protein. MntR was engineered for expression in mammalian cells, and targeted to different subcellular organelles, including the Golgi Apparatus where cellular Mn is enriched. Transfected HEK293 cells and B16 melanoma cells were tested in vitro and in vivo, using immunocytochemistry, MR imaging and relaxometry.

resultsSubcellular targeting of MntR to the cytosol, endoplasmic reticulum and Golgi apparatus was verified with immunocytochemistry. After targeting to the Golgi, MntR expression produced robust R1 changes and T1 contrast in cells, in vitro and in vivo. Co-expression with the divalent metal transporter DMT1, a previously described Mn-based reporter, further enhanced contrast in B16 cells in culture, but in the in vivo B16 tumor model tested was not significantly better than MntR alone.

conclusionThis second-generation reporter system both expands the capabilities of genetically encoded reporters for imaging with MEMRI and provides important insights into the mechanisms of Mn biology which create endogenous MEMRI contrast.

Indexed as

AnimalsBacterial ProteinsCell Line, TumorContrast MediaGenes, ReporterHEK293 CellsHumansMagnetic Resonance ImagingManganeseMiceMice, Inbred C57BLMolecular ProbesMolecular Probe TechniquesNeoplasms, ExperimentalProtein BindingProtein EngineeringBacterial ProteinsContrast MediaManganeseMntR protein, bacteriaMolecular ProbesRepressor ProteinsDMT1manganese (Mn)Mn-enhanced MRI (MEMRI)MntRmolecular imaging

Identifiers

PMID25522343
PMCPMC4470876

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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.