Evidence map›Paper›PMID 30305718›Full record

ArticleScientific reports2018

High-Efficiency Reverse (5'→3') Synthesis of Complex DNA Microarrays.

Kathrin Hölz, Julia K Hoi, Erika Schaudy, Veronika Somoza, Jory Lietard, Mark M Somoza

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
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  8. Review
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  15. Decoding DNA data storage for investment.Biotechnology advances · 2020
    Review
  16. Article
  17. Article
  18. How to copy and paste DNA microarrays.Scientific reports · 2019
    Article
  19. 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.

Kathrin HölzInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Julia K HoiDepartment of Physiological Chemistry, Christian Doppler Laboratory for Bioactive Aroma Compounds, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Erika SchaudyInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Veronika SomozaDepartment of Physiological Chemistry, Christian Doppler Laboratory for Bioactive Aroma Compounds, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Jory LietardInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria. jory.lietard@univie.ac.at.
Mark M SomozaInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria. mark.somoza@univie.ac.at.ORCID http://orcid.org/0000-0002-8039-1341

Funding

Austrian Science Fund FWF P 30596
6 · The paper itself

Abstract

DNA microarrays are important analytical tools in genetics and have recently found multiple new biotechnological roles in applications requiring free 3' terminal hydroxyl groups, particularly as a starting point for enzymatic extension via DNA or RNA polymerases. Here we demonstrate the highly efficient reverse synthesis of complex DNA arrays using a photolithographic approach. The method is analogous to conventional solid phase synthesis but makes use of phosphoramidites with the benzoyl-2-(2-nitrophenyl)-propoxycarbonyl (BzNPPOC) photolabile protecting group on the 3'-hydroxyl group. The use of BzNPPOC, with more than twice the photolytic efficiency of the 2-(2-nitrophenyl)-propoxycarbonyl (NPPOC) previously used for 5'→3' synthesis, combined with additional optimizations to the coupling and oxidation reactions results in an approximately 3-fold improvement in the reverse synthesis efficiency of complex arrays of DNA oligonucleotides. The coupling efficiencies of the reverse phosphoramidites are as good as those of regular phosphoramidites, resulting in comparable yields. Microarrays of DNA surface tethered on the 5' end and with free 3' hydroxyl termini can be synthesized quickly and with similarly high stepwise coupling efficiency as microarrays using conventional 3'→5' synthesis.

Indexed as

DNAFluorescenceGene Expression RegulationOligonucleotide Array Sequence AnalysisOrganophosphorus CompoundsPhotolysisTime FactorsDNAOrganophosphorus Compoundsphosphoramidite

Identifiers

PMID30305718
PMCPMC6180089

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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.