Evidence map›Paper›PMID 30957848›Full record

ArticleNucleic acids research2019

Next-level riboswitch development-implementation of Capture-SELEX facilitates identification of a new synthetic riboswitch.

Adrien Boussebayle, Daniel Torka, Sandra Ollivaud, Johannes Braun, Cristina Bofill-Bosch, Max Dombrowski, Florian Groher, Kay Hamacher, Beatrix Suess

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed.

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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

9 authors.

Adrien BoussebayleDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Daniel TorkaDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Sandra OllivaudDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Johannes BraunDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Cristina Bofill-BoschDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Max DombrowskiComputational Biology and Simulation, Department of Biology, TU Darmstadt, 64287 Darmstadt, Germany.
Florian GroherDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Kay HamacherComputational Biology and Simulation, Department of Biology, TU Darmstadt, 64287 Darmstadt, Germany.
Beatrix SuessDepartment of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of synthetic riboswitches has always been a challenge. Although a number of interesting proof-of-concept studies have been published, almost all of these were performed with the theophylline aptamer. There is no shortage of small molecule-binding aptamers; however, only a small fraction of them are suitable for RNA engineering since a classical SELEX protocol selects only for high-affinity binding but not for conformational switching. We now implemented RNA Capture-SELEX in our riboswitch developmental pipeline to integrate the required selection for high-affinity binding with the equally necessary RNA conformational switching. Thus, we successfully developed a new paromomycin-binding synthetic riboswitch. It binds paromomycin with a KD of 20 nM and can discriminate between closely related molecules both in vitro and in vivo. A detailed structure-function analysis confirmed the predicted secondary structure and identified nucleotides involved in ligand binding. The riboswitch was further engineered in combination with the neomycin riboswitch for the assembly of an orthogonal Boolean NOR logic gate. In sum, our work not only broadens the spectrum of existing RNA regulators, but also signifies a breakthrough in riboswitch development, as the effort required for the design of sensor domains for RNA-based devices will in many cases be much reduced.

Indexed as

SELEX Aptamer TechniqueAptamers, NucleotideLigandsNeomycinNucleic Acid ConformationParomomycinRiboswitchRNASmall Molecule LibrariesStructure-Activity RelationshipTheophyllineAptamers, NucleotideLigandsNeomycinParomomycinRiboswitchRNASmall Molecule LibrariesTheophylline

Identifiers

PMID30957848
PMCPMC6511860

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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.