Evidence map›Paper›PMID 28232577›Full record

ArticleScience (New York, N.Y.)2017

Optical control of cell signaling by single-chain photoswitchable kinases.

Xin X Zhou, Linlin Z Fan, Pengpeng Li, Kang Shen, Michael Z Lin

Open access · bronzeAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
9.4field-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

89 citing papers in PubMed, 199 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Optogenetic control of transition to metamorphosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Review
  9. Disrupted developmental signaling induces novel transcriptional states.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Optogenetic enzymes: A deep dive into design and impact.Current opinion in structural biology · 2025
    Review
  11. Article
  12. Phased ERK responsiveness and developmental robustness regulate teleost skin morphogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Lighting up kinase contacts in situ.Nature chemical biology · 2024
    Article
  19. Article
  20. Article

29 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Xin X ZhouDepartment of Bioengineering, Stanford University, Stanford, CA, USA.ORCID 0000-0001-6681-1568
Linlin Z FanDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Pengpeng LiHoward Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA, USA.
Kang ShenHoward Hughes Medical Institute and Department of Biology, Stanford University, Stanford, CA, USA.
Michael Z LinDepartment of Bioengineering, Stanford University, Stanford, CA, USA. mzlin@stanford.edu.ORCID 0000-0002-0492-1961
Stanford University · USHoward Hughes Medical Institute · US

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI FERRELL, JAMES E. · 2013 to 2017
$10.9M
Optogenetics for all: A general method for optical control of protein activityDP1GM111003 · NIGMS · STANFORD UNIVERSITY · PI LIN, MICHAEL Z. · 2013 to 2017
$4.0M
NIGMS NIH HHS DP1 GM111003NIGMS NIH HHS P50 GM107615
6 · The paper itself

Abstract

Protein kinases transduce signals to regulate a wide array of cellular functions in eukaryotes. A generalizable method for optical control of kinases would enable fine spatiotemporal interrogation or manipulation of these various functions. We report the design and application of single-chain cofactor-free kinases with photoswitchable activity. We engineered a dimeric protein, pdDronpa, that dissociates in cyan light and reassociates in violet light. Attaching two pdDronpa domains at rationally selected locations in the kinase domain, we created the photoswitchable kinases psRaf1, psMEK1, psMEK2, and psCDK5. Using these photoswitchable kinases, we established an all-optical cell-based assay for screening inhibitors, uncovered a direct and rapid inhibitory feedback loop from ERK to MEK1, and mediated developmental changes and synaptic vesicle transport in vivo using light.

Indexed as

AnimalsCaenorhabditis elegansCell Line, TumorDrug Evaluation, PreclinicalExtracellular Signal-Regulated MAP KinasesHumansLightMAP Kinase Kinase 1MutationProtein DomainsProtein EngineeringProtein Kinase InhibitorsProtein MultimerizationSignal TransductionExtracellular Signal-Regulated MAP KinasesMAP Kinase Kinase 1Protein Kinase Inhibitors

Identifiers

PMID28232577
PMCPMC5589340
OpenAlexW2589638834

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.