Evidence map›Paper›PMID 18599625›Full record

ArticleBiophysical journal2008

Fluorescent single-stranded DNA binding protein as a probe for sensitive, real-time assays of helicase activity.

Mark S Dillingham, Katherine L Tibbles, Jackie L Hunter, Jason C Bell, Stephen C Kowalczykowski, Martin R Webb

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Phase separation by ssDNA binding protein controlled via protein-protein and protein-DNA interactions.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
  9. Application of the SSB biosensor to study in vitro transcription.Biochemical and biophysical research communications · 2018
    Article
  10. Article
  11. Article
  12. SSB binds to the RecG and PriA helicases in vivo in the absence of DNA.Genes to cells : devoted to molecular & cellular mechanisms · 2016
    Article
  13. Article
  14. Imaging of DNA and Protein-DNA Complexes with Atomic Force Microscopy.Critical reviews in eukaryotic gene expression · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 2 institutions in 2 countries.

Mark S DillinghamDNA:Protein Interactions Unit, Department of Biochemistry, School of Medical Sciences, University of Bristol, Bristol, United Kingdom.
Katherine L Tibbles
Jackie L Hunter
Jason C Bell
Stephen C Kowalczykowski
Martin R Webb
University of California, Davis · USUniversity of Bristol · GB

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Mechanistic Studies of Genetic RecombinationR01GM062653 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KOWALCZYKOWSKI, STEPHEN CHARLES · 2010 to 2018
$4.4M
MECHANISTIC STUDIES OF GENETIC RECOMBINATIONR37GM062653 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI KOWALCZYKOWSKI, STEPHEN CHARLES · 2000 to 2009
$3.6M
Medical Research Council MC_U117512742NIGMS NIH HHS R01 GM062653NIGMS NIH HHS R37 GM062653NIGMS NIH HHS R37GM-062653NIGMS NIH HHS T32 GM007377NIGMS NIH HHS T32GM-007377Wellcome Trust
6 · The paper itself

Abstract

The formation and maintenance of single-stranded DNA (ssDNA) are essential parts of many processes involving DNA. For example, strand separation of double-stranded DNA (dsDNA) is catalyzed by helicases, and this exposure of the bases on the DNA allows further processing, such as replication, recombination, or repair. Assays of helicase activity and probes for their mechanism are essential for understanding related biological processes. Here we describe the development and use of a fluorescent probe to measure ssDNA formation specifically and in real time, with high sensitivity and time resolution. The reagentless biosensor is based on the ssDNA binding protein (SSB) from Escherichia coli, labeled at a specific site with a coumarin fluorophore. Its use in the study of DNA manipulations involving ssDNA intermediates is demonstrated in assays for DNA unwinding, catalyzed by DNA helicases.

Indexed as

Biological AssayCoumarinsDNA-Binding ProteinsDNA HelicasesDNA, Single-StrandedEscherichia coli ProteinsFluorescenceFluorescent DyesKineticsOsmolar ConcentrationSubstrate SpecificityTime FactorsTryptophanCoumarinsDNA-Binding ProteinsDNA HelicasesDNA, Single-StrandedEscherichia coli ProteinsFluorescent DyesSSB protein, E coliTryptophan

Identifiers

PMID18599625
PMCPMC2547451
OpenAlexW2156463609

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.