Evidence map›Paper›PMID 30719503›Full record

ArticleChem2018

A Massively Parallel Selection of Small Molecule-RNA Motif Binding Partners Informs Design of an Antiviral from Sequence.

Jessica L Childs-Disney, Tuan Tran, Balayeshwanth R Vummidi, Sai Pradeep Velagapudi, Hafeez S Haniff, Yasumasa Matsumoto, Gogce Crynen, Mark R Southern, Avik Biswas, Zi-Fu Wang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Chem, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

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  12. A blood-brain penetrant RNA-targeted small molecule triggers elimination of r(GProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Targeting RNA structures with small molecules.Nature reviews. Drug discovery · 2022
    Review
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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

12 authors at 2 institutions in 2 countries.

Jessica L Childs-DisneyDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Tuan TranDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Balayeshwanth R VummidiDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Sai Pradeep VelagapudiDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Hafeez S HaniffDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Yasumasa MatsumotoDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Gogce CrynenInformatics Core, The Scripps Research Institute, Jupiter, FL 33458, USA.
Mark R SouthernInformatics Core, The Scripps Research Institute, Jupiter, FL 33458, USA.
Avik BiswasDepartment of Immunology & Infectious Diseases, The Scripps Research Institute, Jupiter, FL 33458, USA.
Zi-Fu WangDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Timothy L TellinghuisenDepartment of Immunology & Infectious Diseases, The Scripps Research Institute, Jupiter, FL 33458, USA.
Matthew D DisneyDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, USA.
Scripps Research Institute · USRoche (Switzerland) · CH

Funding

Sequence-based Design of Small Molecules Targeting RNAR01GM097455 · NIGMS · SCRIPPS FLORIDA · PI DISNEY, MATTHEW D · 2012 to 2019
$4.6M
NIGMS NIH HHS R01 GM097455
6 · The paper itself

Abstract

Many RNAs cause disease; however, RNA is rarely exploited as a small-molecule drug target. Our programmatic focus is to define privileged RNA motif small-molecule interactions to enable the rational design of compounds that modulate RNA biology starting from only sequence. We completed a massive, library-versus-library screen that probed over 50 million binding events between RNA motifs and small molecules. The resulting data provide a rich encyclopedia of small-molecule RNA recognition patterns, defining chemotypes and RNA motifs that confer selective, avid binding. The resulting interaction maps were mined against the entire viral genome of hepatitis C virus (HCV). A small molecule was identified that avidly bound RNA motifs present in the HCV 30 UTR and inhibited viral replication while having no effect on host cells. Collectively, this study represents the first whole-genome pattern recognition between small molecules and RNA folds.

Identifiers

PMID30719503
PMCPMC6358276
OpenAlexW2890850847

What OpenQuestion holds

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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.