Evidence map›Paper›PMID 33978414›Full record

ArticleThe journal of physical chemistry. B2021

Optically Modulated and Optically Activated Delayed Fluorescent Proteins through Dark State Engineering.

Baijie Peng, Ryan Dikdan, Shannon E Hill, Athéna C Patterson-Orazem, Raquel L Lieberman, Christoph J Fahrni, Robert M Dickson

Open access · greenAbstract read
In one paragraph

Article in The journal of physical chemistry. B, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Baijie PengSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.
Ryan DikdanSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.
Shannon E HillSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.
Athéna C Patterson-OrazemSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.
Raquel L LiebermanSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.ORCID 0000-0001-9345-3735
Christoph J FahrniSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.ORCID 0000-0003-3731-7434
Robert M DicksonSchool of Chemistry & Biochemistry and Petit Institute for Biosciences and Bioengineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States.ORCID 0000-0003-0042-6194
Georgia Institute of Technology · US

Funding

Request for Supplement to Promote Diversity in Health Related ResearchR01EY021205 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI Raquel L Lieberman · 2011 to 2026
$6.8M
Molecular Tools to Illuminate Copper Transport and HomeostasisR35GM136404 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI FAHRNI, CHRISTOPH J · 2020 to 2024
$2.2M
Phase II SER-CAT Optimization: Acquisition of a next generation area detectorS10RR028976 · NCRR · UNIVERSITY OF GEORGIA · PI WANG, BI-CHENG · 2010 to 2010
$1.5M
Acquition of a microdiffractometer for SER-CATS10RR025528 · NCRR · UNIVERSITY OF GEORGIA · PI ROSE, JOHN PATRICK · 2009 to 2009
$414k
MT-FRET to decode transient protein-protein interactions in Cu homeostasisR21GM134407 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI DICKSON, ROBERT M · 2020 to 2021
$412k
NCRR NIH HHS S10 RR025528NCRR NIH HHS S10 RR028976NEI NIH HHS R01 EY021205NIGMS NIH HHS R21 GM134407NIGMS NIH HHS R35 GM136404
6 · The paper itself

Abstract

Modulating fluorescent protein emission holds great potential for increasing readout sensitivity for applications in biological imaging and detection. Here, we identify and engineer optically modulated yellow fluorescent proteins (EYFP, originally 10C, but renamed EYFP later, and mVenus) to yield new emitters with distinct modulation profiles and unique, optically gated, delayed fluorescence. The parent YFPs are individually modulatable through secondary illumination, depopulating a long-lived dark state to dynamically increase fluorescence. A single point mutation introduced near the chromophore in each of these YFPs provides access to a second, even longer-lived modulatable dark state, while a different double mutant renders EYFP unmodulatable. The naturally occurring dark state in the parent YFPs yields strong fluorescence modulation upon long-wavelength-induced dark state depopulation, allowing selective detection at the frequency at which the long wavelength secondary laser is intensity modulated. Distinct from photoswitches, however, this near IR secondary coexcitation repumps the emissive S

Indexed as

Fluorescent DyesLasersSpectrometry, FluorescenceFluorescent Dyes

Identifiers

PMID33978414
PMCPMC8767457
OpenAlexW3163076289

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.