Evidence map›Paper›PMID 36643573›Full record

ArticleACS omega2023

Forced Intercalation Peptide Nucleic Acid Probes for the Detection of an Adenosine-to-Inosine Modification.

Colin S Swenson, Hector S Argueta-Gonzalez, Sierra A Sterling, Ryan Robichaux, Steve D Knutson, Jennifer M Heemstra

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

6 authors at 1 institution in 1 country.

Colin S SwensonDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.ORCID https://orcid.org/0000-0002-4883-8684
Hector S Argueta-GonzalezDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
Sierra A SterlingDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.ORCID https://orcid.org/0000-0002-0023-8487
Ryan RobichauxDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
Steve D KnutsonDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.ORCID https://orcid.org/0000-0001-6822-464X
Jennifer M HeemstraDepartment of Chemistry, Emory University, Atlanta, Georgia 30322, United States.ORCID https://orcid.org/0000-0002-7691-8526
Emory University · US

Funding

A chemical biology toolbox for RNA post-transcriptional modification and captureR35GM144075 · NIGMS · WASHINGTON UNIVERSITY · PI Jennifer Heemstra · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM144075
6 · The paper itself

Abstract

The deamination of adenosine to inosine is an important modification in nucleic acids that functionally recodes the identity of the nucleobase to a guanosine. Current methods to analyze and detect this single nucleotide change, such as sequencing and PCR, typically require time-consuming or costly procedures. Alternatively, fluorescent "turn-on" probes that result in signal enhancement in the presence of target are useful tools for real-time detection and monitoring of nucleic acid modification. Here we describe forced-intercalation PNA (FIT-PNA) probes that are designed to bind to inosine-containing nucleic acids and use thiazole orange (TO), 4-dimethylamino-naphthalimide (4DMN), and malachite green (MG) fluorogenic dyes to detect A-to-I editing events. We show that incorporation of the dye as a surrogate base negatively affects the duplex stability but does not abolish binding to targets. We then determined that the identity of the adjacent nucleobase and temperature affect the overall signal and fluorescence enhancement in the presence of inosine, achieving an 11-fold increase, with a limit of detection (LOD) of 30 pM. We determine that TO and 4DMN probes are viable candidates to enable selective inosine detection for biological applications.

Identifiers

PMID36643573
PMCPMC9835161
OpenAlexW4312193130

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.