Evidence map›Paper›PMID 16769776›Full record

ArticleNucleic acids research2006

Pyrene binary probes for unambiguous detection of mRNA using time-resolved fluorescence spectroscopy.

Angel A Martí, Xiaoxu Li, Steffen Jockusch, Zengmin Li, Bindu Raveendra, Sergey Kalachikov, James J Russo, Irina Morozova, Sathyanarayanan V Puthanveettil, Jingyue Ju and 1 more

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. DNA/RNA Fluorescence Imaging by Synthetic Nucleic Acids.Advances in experimental medicine and biology · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. DNA-multichromophore systems.Chemical reviews · 2012
    Review
  13. Fluorescent hybridization probes for nucleic acid detection.Analytical and bioanalytical chemistry · 2012
    Review
  14. Mercury(II) ion detection via pyrene-mediated photolysis of disulfide bonds.Chemistry (Weinheim an der Bergstrasse, Germany) · 2012
    Article
  15. Review
  16. Nucleic acid-based fluorescent probes and their analytical potential.Analytical and bioanalytical chemistry · 2011
    Review
  17. Article
  18. Article
  19. Review
  20. Telomeric repeat-containing RNA structure in living cells.Proceedings of the National Academy of Sciences of the United States of America · 2010
    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

11 authors.

Angel A MartíDepartment of Chemistry, Columbia University, New York, NY 10027, USA.
Xiaoxu Li
Steffen Jockusch
Zengmin Li
Bindu Raveendra
Sergey Kalachikov
James J Russo
Irina Morozova
Sathyanarayanan V Puthanveettil
Jingyue Ju
Nicholas J Turro

Funding

Genomic Approaches to Neuronal Diversity and PlasticityP50HG002806 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JU, JINGYUE · 2003 to 2007
$13.9M
NHGRI NIH HHS P50 HG002806
6 · The paper itself

Abstract

We report here the design, synthesis and application of pyrene binary oligonucleotide probes for selective detection of cellular mRNA. The detection strategy is based on the formation of a fluorescent excimer when two pyrene groups are brought into close proximity upon hybridization of the probes with the target mRNA. The pyrene excimer has a long fluorescence lifetime (>40 ns) compared with that of cellular extracts (approximately 7 ns), allowing selective detection of the excimer using time-resolved emission spectra (TRES). Optimized probes were used to target a specific region of sensorin mRNA yielding a strong excimer emission peak at 485 nm in the presence of the target and no excimer emission in the absence of the target in buffer solution. While direct fluorescence measurement of neuronal extracts showed a strong fluorescent background, obscuring the detection of the excimer signal, time-resolved emission measurements indicated that the emission decay of the cellular extracts is approximately 8 times faster than that of the pyrene excimer probes. Thus, using TRES of the pyrene probes, we are able to selectively detect mRNA in the presence of cellular extracts, demonstrating the potential for application of pyrene excimer probes for imaging mRNAs in cellular environments that have background fluorescence.

Indexed as

AnimalsAplysiaCell ExtractsFluorescent DyesInsect ProteinsNeuronsNeuropeptidesOligonucleotide ProbesPyrenesRNA, MessengerSpectrometry, FluorescenceTime FactorsCell ExtractsFluorescent DyesInsect ProteinsNeuropeptidesOligonucleotide ProbesPyrenesRNA, Messenger

Identifiers

PMID16769776
PMCPMC1477857

What OpenQuestion holds

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LicenceCC BY-NC
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.