Evidence map›Paper›PMID 24358989›Full record

ArticleBioconjugate chemistry2014

Efficient access to 3'-terminal azide-modified RNA for inverse click-labeling patterns.

Tobias Santner, Markus Hartl, Klaus Bister, Ronald Micura

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 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

4 authors.

Tobias SantnerInstitute of Organic Chemistry and ‡Institute of Biochemistry, Center for Molecular Biosciences CMBI, University of Innsbruck , 6020 Innsbruck, Austria.
Markus Hartl
Klaus Bister
Ronald Micura

Funding

Austrian Science Fund FWF P 21641Austrian Science Fund FWF P 23652
6 · The paper itself

Abstract

Labeled RNA becomes increasingly important for molecular diagnostics and biophysical studies on RNA with its diverse interaction partners, which range from small metabolites to large macromolecular assemblies, such as the ribosome. Here, we introduce a fast synthesis path to 3'-terminal 2'-O-(2-azidoethyl) modified oligoribonucleotides for subsequent bioconjugation, as exemplified by fluorescent labeling via Click chemistry for an siRNA targeting the brain acid-soluble protein 1 gene (BASP1). Importantly, the functional group pattern is inverse to commonly encountered alkyne-functionalized "click"-able RNA and offers increased flexibility with respect to multiple and stepwise labeling of the same RNA molecule. Additionally, our route opens up a minimal step synthesis of 2'-O-(2-aminoethyl) modified pyrimidine nucleoside phosphoramidites which are of widespread use to generate amino-modified RNA for N-hydroxysuccinimide (NHS) ester-based conjugations.

Indexed as

AnimalsAzidesCell LineChickensClick ChemistryCytoskeletal ProteinsFluorescenceMicroscopy, FluorescenceMolecular StructureOligoribonucleotidesRNA, MessengerRNA, Small InterferingAzidesCytoskeletal ProteinsOligoribonucleotidesRNA, MessengerRNA, Small Interfering

Identifiers

PMID24358989
PMCPMC3898571

What OpenQuestion holds

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Registered trials

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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.