Evidence map›Paper›PMID 25337688›Full record

ArticleJournal of the American Chemical Society2014

Broccoli: rapid selection of an RNA mimic of green fluorescent protein by fluorescence-based selection and directed evolution.

Grigory S Filonov, Jared D Moon, Nina Svensen, Samie R Jaffrey

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 358 papers.

0numbers the graph read from it
0cells of the map it votes in
358citing papers in PubMed
15.5field-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

358 citing papers in PubMed, 774 citations in OpenAlex.

  1. A miniature bioluminescent platform for imaging structured RNAs.bioRxiv : the preprint server for biology · 2026
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  6. Honeydew: A Fluorescent Aptamer for Low-Cost Azo Food Dyes.Chembiochem : a European journal of chemical biology · 2026
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298 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

4 authors at 1 institution in 1 country.

Grigory S FilonovDepartment of Pharmacology, Weill Cornell Medical College , New York, New York 10065, United States.
Jared D Moon
Nina Svensen
Samie R Jaffrey
Cornell University · US

Funding

Engineering RNA-activated fluorescence switches for RNA imaging and analyte sensiR01NS064516 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2018
$3.6M
Novel fluorescent sensors for simple, sensitive, and specific protein detectionR01EB010249 · NIBIB · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2013
$1.7M
NIBIB NIH HHS R01 EB010249NINDS NIH HHS R01 NS064516
6 · The paper itself

Abstract

Genetically encoded fluorescent ribonucleic acids (RNAs) have diverse applications, including imaging RNA trafficking and as a component of RNA-based sensors that exhibit fluorescence upon binding small molecules in live cells. These RNAs include the Spinach and Spinach2 aptamers, which bind and activate the fluorescence of fluorophores similar to that found in green fluorescent protein. Although additional highly fluorescent RNA-fluorophore complexes would extend the utility of this technology, the identification of novel RNA-fluorophore complexes is difficult. Current approaches select aptamers on the basis of their ability to bind fluorophores, even though fluorophore binding alone is not sufficient to activate fluorescence. Additionally, aptamers require extensive mutagenesis to efficiently fold and exhibit fluorescence in living cells. Here we describe a platform for rapid generation of highly fluorescent RNA-fluorophore complexes that are optimized for function in cells. This procedure involves selection of aptamers on the basis of their binding to fluorophores, coupled with fluorescence-activated cell sorting (FACS) of millions of aptamers expressed in Escherichia coli. Promising aptamers are then further optimized using a FACS-based directed evolution approach. Using this approach, we identified several novel aptamers, including a 49-nt aptamer, Broccoli. Broccoli binds and activates the fluorescence of (Z)-4-(3,5-difluoro-4-hydroxybenzylidene)-1,2-dimethyl-1H-imidazol-5(4H)-one. Broccoli shows robust folding and green fluorescence in cells, and increased fluorescence relative to Spinach2. This reflects, in part, improved folding in the presence of low cytosolic magnesium concentrations. Thus, this novel fluorescence-based selection approach simplifies the generation of aptamers that are optimized for expression and performance in living cells.

Indexed as

Directed Molecular EvolutionSELEX Aptamer TechniqueAptamers, NucleotideBase SequenceBenzyl CompoundsBiomimetic MaterialsDimerizationGreen Fluorescent ProteinsHEK293 CellsHumansImidazolinesInverted Repeat SequencesMolecular ImagingRNA StabilitySpectrometry, FluorescenceTemperature3,5-difluoro-4-hydroxybenzylidene imidazolinoneAptamers, NucleotideBenzyl CompoundsGreen Fluorescent ProteinsImidazolines

Identifiers

PMID25337688
PMCPMC4244833
OpenAlexW2332645767

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.