Cited by 780RNA and protein synthesis mechanismsAdvanced biosensing and bioanalysis techniquesDNA and Nucleic Acid Chemistry

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

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Filonov, Grigory S., Moon, Jared D., Svensen, Nina, Jaffrey, Samie R.·2014·Journal of the American Chemical Society

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.

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Authors
Filonov, G. S., Moon, J. D., Svensen, N., & Jaffrey, S. R.
Affiliations
Cornell University (US)
Corresponding author
Jaffrey, Samie R.
Venue
Journal of the American Chemical Society
Published
2014-10-22
Volume
136
Issue
46
Pages
16299-16308
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2332645767
Cited by
780
References
34
Citations by year
2026: 63 · 2025: 78 · 2024: 93 · 2023: 73 · 2022: 67 · 2021: 78 · 2020: 82 · 2019: 77 · 2018: 60 · 2017: 57 · 2016: 31 · 2015: 20 · 2014: 1
FWCI
14.89
Type
journal article
Language
en
Open access
Locations
  • Journal of the American Chemical Society (publishedVersion, other-oa)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute of Neurological Disorders and Stroke (R01 NS064516)
  • National Institute of Biomedical Imaging and Bioengineering (R01 EB010249)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced biosensing and bioanalysis techniques
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
Keywords
fluorescence-activated cell sorting, directed evolution, RNA folding, Escherichia coli
MeSH terms
Base Sequence, Benzyl Compounds, Humans, Spectrometry, Fluorescence, Temperature, Directed Molecular Evolution, Dimerization, RNA Stability, Biomimetic Materials, Imidazolines, Green Fluorescent Proteins, SELEX Aptamer Technique, Aptamers, Nucleotide, Inverted Repeat Sequences, Molecular Imaging, HEK293 Cells

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