Evidence map›Paper›PMID 28262559›Full record

ArticleCell chemical biology2017

Directed Evolution of a Bright Near-Infrared Fluorescent Rhodopsin Using a Synthetic Chromophore.

Lukas Herwig, Austin J Rice, Claire N Bedbrook, Ruijie K Zhang, Antti Lignell, Jackson K B Cahn, Hans Renata, Sheel C Dodani, Inha Cho, Long Cai and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 64 citations in OpenAlex.

  1. De Novo Design of Near-Infrared Fluorescence-Activating Proteins.Journal of the American Chemical Society · 2026
    Article
  2. Review
  3. Merocyanines form bacteriorhodopsins with strongly bathochromic absorption maxima.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Imaging Voltage with Microbial Rhodopsins.Frontiers in molecular biosciences · 2021
    Review
  13. Article
  14. Review
  15. Genetically Encoded Activators of Small Molecules for Imaging and Drug Delivery.Angewandte Chemie (International ed. in English) · 2020
    Review
  16. Review
  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

12 authors at 1 institution in 1 country.

Lukas HerwigDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Austin J RiceDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Claire N BedbrookDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA; Division of Biology and Biological Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Ruijie K ZhangDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Antti LignellDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Jackson K B CahnDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Hans RenataDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Sheel C DodaniDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Inha ChoDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Long CaiDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Viviana GradinaruDivision of Biology and Biological Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA.
Frances H ArnoldDivision of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA; Division of Biology and Biological Engineering, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA. Electronic address: frances@cheme.caltech.edu.
California Institute of Technology · US

Funding

Engineering Microbial Opsins for Neuroscience via Structure-Guided RecombinationR21MH103824 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ARNOLD, FRANCES H, GRADINARU, VIVIANA · 2014 to 2015
$458k
SIG Program: AKTAxpress FPLC System for Protein PurificationS10RR027203 · NCRR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ARNOLD, FRANCES H · 2010 to 2010
$176k
Biocatalytic Use of Cytochrome P450 EnzymesF32GM106618 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI DODANI, SHEEL · 2013 to 2015
$145k
Structural characterization and structure-based engineering of channelrhodopsins for neurobiologyF32GM116319 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI RICE, AUSTIN J. · 2015 to 2017
$119k
Opsineering: Engineering Novel ChannelRhodospins for Optogenetics ApplicationsF31MH102913 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BEDBROOK, CLAIRE NICOLE · 2014 to 2016
$110k
NCRR NIH HHS S10 RR027203NIGMS NIH HHS F32 GM106618NIGMS NIH HHS F32 GM116319NIMH NIH HHS F31 MH102913NIMH NIH HHS R21 MH103824
6 · The paper itself

Abstract

By engineering a microbial rhodopsin, Archaerhodopsin-3 (Arch), to bind a synthetic chromophore, merocyanine retinal, in place of the natural chromophore all-trans-retinal (ATR), we generated a protein with exceptionally bright and unprecedentedly red-shifted near-infrared (NIR) fluorescence. We show that chromophore substitution generates a fluorescent Arch complex with a 200-nm bathochromic excitation shift relative to ATR-bound wild-type Arch and an emission maximum at 772 nm. Directed evolution of this complex produced variants with pH-sensitive NIR fluorescence and molecular brightness 8.5-fold greater than the brightest ATR-bound Arch variant. The resulting proteins are well suited to bacterial imaging; expression and stability have not been optimized for mammalian cell imaging. By targeting both the protein and its chromophore, we overcome inherent challenges associated with engineering bright NIR fluorescence into Archaerhodopsin. This work demonstrates an efficient strategy for engineering non-natural, tailored properties into microbial opsins, properties relevant for imaging and interrogating biological systems.

Indexed as

Directed Molecular EvolutionBinding SitesEscherichia coliHydrogen-Ion ConcentrationIsomerismKineticsMicroscopy, FluorescenceMolecular Docking SimulationMutagenesis, Site-DirectedProtein Structure, TertiaryRetinaldehydeRhodopsinSpectroscopy, Near-InfraredRetinaldehydeRhodopsinArchaerhodopsindirected evolutionlive-cell imagingnear-infrared fluorescenceprotein engineeringsynthetic chromophore substitution

Identifiers

PMID28262559
PMCPMC5357175
OpenAlexW2594189097

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.