Evidence map›Paper›PMID 25350266›Full record

ArticleACS synthetic biology2014

Benchmarking of optical dimerizer systems.

Gopal P Pathak, Devin Strickland, Justin D Vrana, Chandra L Tucker

Open access · bronzeAbstract read
In one paragraph

Article in ACS synthetic biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
14.0field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 97 citations in OpenAlex.

  1. Engineered Optogenetic Circuits In Yeast with Self-Sustained Outputs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Circular dichroism spectroscopy reveals multiple phytochrome photoproducts in equilibrium.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Construction and Characterization of Light-Responsive Transcriptional Systems.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Engineering Light-Control in Biology.Frontiers in bioengineering and biotechnology · 2022
    Review
  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

4 authors at 2 institutions in 1 country.

Gopal P PathakDepartment of Pharmacology, University of Colorado School of Medicine , Aurora, Colorado 80045, United States.
Devin Strickland
Justin D Vrana
Chandra L Tucker
University of Colorado Denver · USUniversity of Chicago · US

Funding

Control of Protein Activity Via Light Stimulated DimerizersR01GM100225 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI TUCKER, CHANDRA L · 2012 to 2019
$3.3M
Spatial and temporal control of cell behavior with a genetically-encoded photoswiR01GM088668 · NIGMS · UNIVERSITY OF CHICAGO · PI GLOTZER, MICHAEL A., SOSNICK, TOBIN R · 2009 to 2012
$1.4M
NIGMS NIH HHS GM088668NIGMS NIH HHS GM100225NIGMS NIH HHS R01 GM088668NIGMS NIH HHS R01 GM100225
6 · The paper itself

Abstract

Optical dimerizers are a powerful new class of optogenetic tools that allow light-inducible control of protein-protein interactions. Such tools have been useful for regulating cellular pathways and processes with high spatiotemporal resolution in live cells, and a growing number of dimerizer systems are available. As these systems have been characterized by different groups using different methods, it has been difficult for users to compare their properties. Here, we set about to systematically benchmark the properties of four optical dimerizer systems, CRY2/CIB1, TULIPs, phyB/PIF3, and phyB/PIF6. Using a yeast transcriptional assay, we find significant differences in light sensitivity and fold-activation levels between the red light regulated systems but similar responses between the CRY2/CIB and TULIP systems. Further comparison of the ability of the CRY2/CIB1 and TULIP systems to regulate a yeast MAPK signaling pathway also showed similar responses, with slightly less background activity in the dark observed with CRY2/CIB. In the process of developing this work, we also generated an improved blue-light-regulated transcriptional system using CRY2/CIB in yeast. In addition, we demonstrate successful application of the CRY2/CIB dimerizers using a membrane-tethered CRY2, which may allow for better local control of protein interactions. Taken together, this work allows for a better understanding of the capacities of these different dimerization systems and demonstrates new uses of these dimerizers to control signaling and transcription in yeast.

Indexed as

CryptochromesDimerizationExtracellular Signal-Regulated MAP KinasesOptogeneticsPhytochromeProtein Structure, TertiarySignal TransductionTranscription, GeneticYeastsCryptochromesExtracellular Signal-Regulated MAP KinasesPhytochromecryptochromelight controlLOV domainoptogeneticsphotoreceptorphytochrometranscription

Identifiers

PMID25350266
PMCPMC4277767
OpenAlexW2071764758

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.