Evidence map›Paper›PMID 28088361›Full record

ArticleJournal of chromatography. A2017

Purification and characterisation of dsRNA using ion pair reverse phase chromatography and mass spectrometry.

Alison O Nwokeoji, An-Wen Kung, Peter M Kilby, David E Portwood, Mark J Dickman

Open access · hybridAbstract read
In one paragraph

Article in Journal of chromatography. A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Optimizing dsRNA engineering strategies and production in E. coli HT115 (DE3).Journal of industrial microbiology & biotechnology · 2024
    Article
  10. Anion exchange HPLC monitoring of mRNAFrontiers in molecular biosciences · 2024
    Article
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  18. 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

5 authors at 2 institutions in 1 country.

Alison O NwokeojiDepartment of Chemical and Biological Engineering, ChELSI Institute, Mappin Street, University of Sheffield, S1 3JD, UK.
An-Wen KungDepartment of Chemical and Biological Engineering, ChELSI Institute, Mappin Street, University of Sheffield, S1 3JD, UK.
Peter M KilbySyngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire, RG42 6EY, UK.
David E PortwoodSyngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire, RG42 6EY, UK.
Mark J DickmanDepartment of Chemical and Biological Engineering, ChELSI Institute, Mappin Street, University of Sheffield, S1 3JD, UK. Electronic address: m.dickman@sheffield.ac.uk.
University of Sheffield · GBSyngenta (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M012166/1
6 · The paper itself

Abstract

RNA interference has provided valuable insight into a wide range of biological systems and is a powerful tool for the analysis of gene function. The exploitation of this pathway to block the expression of specific gene targets holds considerable promise for the development of novel RNAi-based insect management strategies. In addition, there are a wide number of future potential applications of RNAi to control agricultural insect pests as well as its use for prevention of diseases in beneficial insects. The potential to synthesise large quantities of dsRNA by in-vitro transcription or in bacterial systems for RNA interference applications has generated significant demand for the development and application of high throughput analytical tools for the rapid extraction, purification and analysis of dsRNA. Here we have developed analytical methods that enable the rapid purification of dsRNA from associated impurities from bacterial cells in conjunction with downstream analyses. We have optimised TRIzol extractions in conjunction with a single step protocol to remove contaminating DNA and ssRNA, using RNase T1/DNase I digestion under high-salt conditions in combination with solid phase extraction to purify the dsRNA. In addition, we have utilised and developed IP RP HPLC for the rapid, high resolution analysis of the dsRNA. Furthermore, we have optimised base-specific cleavage of dsRNA by RNase A and developed a novel method utilising RNase T1 for RNase mass mapping approaches to further characterise the dsRNA using liquid chromatography interfaced with mass spectrometry.

Indexed as

Chromatography, High Pressure LiquidMass SpectrometryAnimalsChromatography, Reverse-PhaseInsectaRibonuclease, PancreaticRNA, Double-StrandedRNA InterferenceSequence Analysis, RNARibonuclease, PancreaticRNA, Double-StrandedDouble stranded RNA purificationIon pair reverse phase HPLCMass spectrometryRNase mass mapping

Identifiers

PMID28088361
PMCPMC5267946
OpenAlexW2564791984

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.