Evidence map›Paper›PMID 17697378›Full record

ArticleBMC biotechnology2007

One-step selection of Vaccinia virus-binding DNA aptamers by MonoLEX.

Andreas Nitsche, Andreas Kurth, Anna Dunkhorst, Oliver Pänke, Hendrik Sielaff, Wolfgang Junge, Doreen Muth, Frieder Scheller, Walter Stöcklein, Claudia Dahmen and 2 more

Abstract read
In one paragraph

Article in BMC biotechnology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Aptasensors versus immunosensors-Which will prevail?Engineering in life sciences · 2022
    Review
  6. Article
  7. Single-round deoxyribozyme discovery.Nucleic acids research · 2021
    Article
  8. Review
  9. Review
  10. Engineered Aptamers for Enhanced COVID-19 Theranostics.Cellular and molecular bioengineering · 2021
    Review
  11. Review
  12. SELEX-based DNA Aptamer Selection: A Perspective from the Advancement of Separation Techniques.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2021
    Review
  13. Aptamers: An Emerging Tool for Diagnosis and Therapeutics in Tuberculosis.Frontiers in cellular and infection microbiology · 2021
    Review
  14. Review
  15. Article
  16. Review
  17. Updates on Aptamer Research.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  20. Review
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.

Andreas NitscheCentre for Biological Safety 1, Robert Koch-Institut, Nordufer 20, 13353 Berlin, Germany. nitsche@rki.de
Andreas Kurth
Anna Dunkhorst
Oliver Pänke
Hendrik Sielaff
Wolfgang Junge
Doreen Muth
Frieder Scheller
Walter Stöcklein
Claudia Dahmen
Georg Pauli
Andreas Kage

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a new class of therapeutic and diagnostic reagents, more than fifteen years ago RNA and DNA aptamers were identified as binding molecules to numerous small compounds, proteins and rarely even to complete pathogen particles. Most aptamers were isolated from complex libraries of synthetic nucleic acids by a process termed SELEX based on several selection and amplification steps. Here we report the application of a new one-step selection method (MonoLEX) to acquire high-affinity DNA aptamers binding Vaccinia virus used as a model organism for complex target structures.

resultsThe selection against complete Vaccinia virus particles resulted in a 64-base DNA aptamer specifically binding to orthopoxviruses as validated by dot blot analysis, Surface Plasmon Resonance, Fluorescence Correlation Spectroscopy and real-time PCR, following an aptamer blotting assay. The same oligonucleotide showed the ability to inhibit in vitro infection of Vaccinia virus and other orthopoxviruses in a concentration-dependent manner.

conclusionThe MonoLEX method is a straightforward procedure as demonstrated here for the identification of a high-affinity DNA aptamer binding Vaccinia virus. MonoLEX comprises a single affinity chromatography step, followed by subsequent physical segmentation of the affinity resin and a single final PCR amplification step of bound aptamers. Therefore, this procedure improves the selection of high affinity aptamers by reducing the competition between aptamers of different affinities during the PCR step, indicating an advantage for the single-round MonoLEX method.

Indexed as

Aptamers, NucleotideChromatography, AffinityDNA, ViralGene TargetingPolymerase Chain ReactionVaccinia virusAptamers, NucleotideDNA, Viral

Identifiers

PMID17697378
PMCPMC1994675

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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.