Evidence map›Paper›PMID 26857021›Full record

ArticleScientific reports2016

A molecular nanodevice for targeted degradation of mRNA during protein synthesis.

Kyung-Ho Lee, Seung-Eui Min, Haseong Kim, Seung-Goo Lee, Dong-Myung Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. 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
0.5field-weighted citation impact, top 29% 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, 7 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

5 authors at 2 institutions in 1 country.

Kyung-Ho LeeDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon 305-764, Korea.
Seung-Eui MinDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon 305-764, Korea.
Haseong KimSynthetic Biology and Bioengineering Research Center, KRIBB, Daejeon 34141, Korea.
Seung-Goo LeeSynthetic Biology and Bioengineering Research Center, KRIBB, Daejeon 34141, Korea.
Dong-Myung KimDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon 305-764, Korea.
Chungnam National University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNase H is an endonuclease that catalyzes the cleavage of RNA. Because it only acts on RNA in RNA:DNA hybrids, RNase H can be used for targeted degradation of RNA when used in combination with antisense oligodeoxyribonucleotides (ASODNs) designed against a specific sequence of the target RNA. In this study, ASODN and RNase H were co-conjugated on magnetic nanoparticles. The resulting nanoparticles, having integrated functions of probing and processing target RNA, were able to remove target mRNA sequences more effectively than free ASODNs. The paramagnetic property of the nanoparticles also enabled timed engagement and disengagement of the RNA-degrading components in a given system, and these nanoparticles were able to be used for ON/OFF control of gene expression during cell-free protein synthesis reactions.

Indexed as

Protein BiosynthesisRNA StabilityCell-Free SystemMagnetite NanoparticlesOligodeoxyribonucleotides, AntisenseRibonuclease HRNA, MessengerMagnetite NanoparticlesOligodeoxyribonucleotides, AntisenseRibonuclease HRNA, Messenger

Identifiers

PMID26857021
PMCPMC4746582
OpenAlexW2418235748

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.