Evidence map›Paper›PMID 19740766›Full record

ArticleNucleic acids research2009

High-resolution profiling of homing endonuclease binding and catalytic specificity using yeast surface display.

Jordan Jarjour, Hoku West-Foyle, Michael T Certo, Christopher G Hubert, Lindsey Doyle, Melissa M Getz, Barry L Stoddard, Andrew M Scharenberg

Abstract read
In one paragraph

Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Gene Drive for Mosquito Control: Where Did It Come from and Where Are We Headed?International journal of environmental research and public health · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Salient Features of Endonuclease Platforms for Therapeutic Genome Editing.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Review
  13. The Development of TALE Nucleases for Biotechnology.Methods in molecular biology (Clifton, N.J.) · 2016
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Redesign of extensive protein-DNA interfaces of meganucleases using iterative cycles of in vitro compartmentalization.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

8 authors.

Jordan JarjourDepartment of Immunology, University of Washington, Seattle, WA 98195, USA.
Hoku West-Foyle
Michael T Certo
Christopher G Hubert
Lindsey Doyle
Melissa M Getz
Barry L Stoddard
Andrew M Scharenberg

Funding

Cell and Virus COREPL1HL092557 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI RAWLINGS, DAVID J · 2007 to 2011
$4.3M
Northwest Genome Engineering Consortium (Component 1 of 11)UL1DE019582 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI SCHARENBERG, ANDREW M. · 2008 to 2011
$3.1M
Directed Protein Evolution for Design of LAGLIDADGs with Novel Recognition SpeciRL1CA133832 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI SCHARENBERG, ANDREW M. · 2007 to 2011
$2.2M
Structural and Biophysical Characterization of Engineered Homing Endonucleases (CRL1CA133833 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STODDARD, BARRY L. · 2007 to 2011
$2.1M
NCI NIH HHS #RL1CA133832NCI NIH HHS RL1CA133832NCI NIH HHS RL1 CA133833NCI NIH HHS RL1CA133833NHLBI NIH HHS PL1HL092557NIDCR NIH HHS UL1DE019582
6 · The paper itself

Abstract

Experimental analysis and manipulation of protein-DNA interactions pose unique biophysical challenges arising from the structural and chemical homogeneity of DNA polymers. We report the use of yeast surface display for analytical and selection-based applications for the interaction between a LAGLIDADG homing endonuclease and its DNA target. Quantitative flow cytometry using oligonucleotide substrates facilitated a complete profiling of specificity, both for DNA-binding and catalysis, with single base pair resolution. These analyses revealed a comprehensive segregation of binding specificity and affinity to one half of the pseudo-dimeric interaction, while the entire interface contributed specificity at the level of catalysis. A single round of targeted mutagenesis with tandem affinity and catalytic selection steps provided mechanistic insights to the origins of binding and catalytic specificity. These methods represent a dynamic new approach for interrogating specificity in protein-DNA interactions.

Indexed as

Binding SitesCatalysisDeoxyribonucleases, Type II Site-SpecificDNADNA Restriction EnzymesEndonucleasesFlow CytometryModels, MolecularSaccharomyces cerevisiaeSubstrate SpecificityDeoxyribonucleases, Type II Site-SpecificDNADNA Restriction EnzymesEndonucleases

Identifiers

PMID19740766
PMCPMC2777416

What OpenQuestion holds

Textmetadata
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.