Evidence map›Paper›PMID 26114964›Full record

ArticleRNA biology2015

A minimalist biosensor: Quantitation of cyclic di-GMP using the conformational change of a riboswitch aptamer.

Colleen A Kellenberger, Jade Sales-Lee, Yuchen Pan, Madalee M Gassaway, Amy E Herr, Ming C Hammond

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Tools and systems for evolutionary engineering of biomolecules and microorganisms.Journal of industrial microbiology & biotechnology · 2019
    Review
  4. Article
  5. From fluorescent proteins to fluorogenic RNAs: Tools for imaging cellular macromolecules.Protein science : a publication of the Protein Society · 2019
    Review
  6. Article
  7. Article
  8. Evaluating riboswitch optimality.Methods in enzymology · 2019
    Article
  9. Article
  10. Article
  11. Live Flow Cytometry Analysis of c-di-GMP Levels in Single Cell Populations.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  12. Review
  13. 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

6 authors at 3 institutions in 2 countries.

Colleen A Kellenbergera Department of Chemistry ; University of California, Berkeley ; Berkeley , CA USA.
Jade Sales-Leea Department of Chemistry ; University of California, Berkeley ; Berkeley , CA USA.
Yuchen Panb Graduate Program in Bioengineering; University of California, Berkeley ; Berkeley , CA USA.
Madalee M Gassawaya Department of Chemistry ; University of California, Berkeley ; Berkeley , CA USA.
Amy E Herrb Graduate Program in Bioengineering; University of California, Berkeley ; Berkeley , CA USA.
Ming C Hammonda Department of Chemistry ; University of California, Berkeley ; Berkeley , CA USA.
University of California, Berkeley · USBerkeley College · USBioengineering Center · RU

Funding

Univ of Calif Berkeley Chemistry-Biology Interface ProgramT32GM066698 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI CHANG, CHRISTOPHER J., FRANCIS, MATTHEW B · 2004 to 2023
$7.5M
A Chemical Biology Approach to Tagging RNAs in Live CellsDP2OD008677 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI HAMMOND, MING CHEN · 2011 to 2011
$2.3M
NIGMS NIH HHS T32 GM066698NIH HHS 1DP2OD008677NIH HHS DP2 OD008677
6 · The paper itself

Abstract

Cyclic di-GMP (c-di-GMP) is a second messenger that is important in regulating bacterial physiology and behavior, including motility and virulence. Many questions remain about the role and regulation of this signaling molecule, but current methods of detection are limited by either modest sensitivity or requirements for extensive sample purification. We have taken advantage of a natural, high affinity receptor of c-di-GMP, the Vc2 riboswitch aptamer, to develop a sensitive and rapid electrophoretic mobility shift assay (EMSA) for c-di-GMP quantitation that required minimal engineering of the RNA.

Indexed as

Aptamers, NucleotideBiosensing TechniquesRiboswitchBase SequenceCyclic GMPElectrophoretic Mobility Shift AssayEscherichia coliMutationNucleic Acid ConformationSecond Messenger SystemsSignal TransductionAptamers, Nucleotidebis(3',5')-cyclic diguanylic acidCyclic GMPRiboswitchbacterial signalingcyclic AMP-GMPcyclic dinucleotidesligand bindingmicrofluidic mobility shift assaynative EMSA

Identifiers

PMID26114964
PMCPMC4829349
OpenAlexW2175154535

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.