Evidence map›Paper›PMID 29466657›Full record

ArticleACS chemical biology2018

Chemiluminescent Biosensors for Detection of Second Messenger Cyclic di-GMP.

Andrew B Dippel, Wyatt A Anderson, Robert S Evans, Samuel Deutsch, Ming C Hammond

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
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  9. Visualization of c-di-GMP in multicellularFrontiers in cell and developmental biology · 2023
    Article
  10. Article
  11. Article
  12. Analyzing signaling activity and function in hematopoietic cells.The Journal of experimental medicine · 2021
    Review
  13. Article
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  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Andrew B DippelDepartment of Chemistry , University of California , Berkeley , California 94720 , United States.
Wyatt A AndersonDepartment of Chemistry , University of California , Berkeley , California 94720 , United States.
Robert S EvansDOE Joint Genome Institute , 2800 Mitchell Drive , Walnut Creek , California 94598 , United States.
Samuel DeutschDOE Joint Genome Institute , 2800 Mitchell Drive , Walnut Creek , California 94598 , United States.
Ming C HammondDepartment of Chemistry , University of California , Berkeley , California 94720 , United States.ORCID 0000-0003-2666-4764
Joint Genome Institute · USUniversity of California, Berkeley · USLawrence Berkeley National Laboratory · US

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
Enabling High-Throughput Analysis and Single-Cell Imaging of Bacterial SignalsR01GM124589 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HAMMOND, MING CHEN · 2017 to 2025
$2.8M
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 R01 GM124589NIGMS NIH HHS T32 GM066698NIH HHS DP2 OD008677
6 · The paper itself

Abstract

Bacteria colonize highly diverse and complex environments, from gastrointestinal tracts to soil and plant surfaces. This colonization process is controlled in part by the intracellular signal cyclic di-GMP, which regulates bacterial motility and biofilm formation. To interrogate cyclic di-GMP signaling networks, a variety of fluorescent biosensors for live cell imaging of cyclic di-GMP have been developed. However, the need for external illumination precludes the use of these tools for imaging bacteria in their natural environments, including in deep tissues of whole organisms and in samples that are highly autofluorescent or photosensitive. The need for genetic encoding also complicates the analysis of clinical isolates and environmental samples. Toward expanding the study of bacterial signaling to these systems, we have developed the first chemiluminescent biosensors for cyclic di-GMP. The biosensor design combines the complementation of split luciferase (CSL) and bioluminescence resonance energy transfer (BRET) approaches. Furthermore, we developed a lysate-based assay for biosensor activity that enabled reliable high-throughput screening of a phylogenetic library of 92 biosensor variants. The screen identified biosensors with very large signal changes (∼40- and 90-fold) as well as biosensors with high affinities for cyclic di-GMP ( K

Indexed as

Amino Acid SequenceBase SequenceBiosensing TechniquesCyclic GMPEscherichia coliEscherichia coli ProteinsFluorescenceLuminescent ProteinsMutationPhylogenySecond Messenger Systemsbis(3',5')-cyclic diguanylic acidCyclic GMPEscherichia coli ProteinsLuminescent ProteinsYcgR protein, E coli

Identifiers

PMID29466657
PMCPMC6054565
OpenAlexW2787907248

What OpenQuestion holds

Textmetadata
LicenceTDM
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.