Evidence map›Paper›PMID 28265062›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Selection of DNA aptamers with two modified bases.

Bharat N Gawande, John C Rohloff, Jeffrey D Carter, Ira von Carlowitz, Chi Zhang, Daniel J Schneider, Nebojsa Janjic

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
10.6field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 192 citations in OpenAlex.

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  16. Selection of structure-induced aptamer targeting small molecule based on capillary sieving electrophoresis.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2024
    Article
  17. Review
  18. Assessment of the structural change of DNA by binding with a small molecule based on capillary sieving electrophoresis.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2024
    Article
  19. Article
  20. Review

20 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Bharat N GawandeSomaLogic, Inc., Boulder, CO 80301.
John C RohloffSomaLogic, Inc., Boulder, CO 80301.
Jeffrey D CarterSomaLogic, Inc., Boulder, CO 80301.
Ira von CarlowitzSomaLogic, Inc., Boulder, CO 80301.
Chi ZhangSomaLogic, Inc., Boulder, CO 80301.
Daniel J SchneiderSomaLogic, Inc., Boulder, CO 80301.
Nebojsa JanjicSomaLogic, Inc., Boulder, CO 80301 njanjic@somalogic.com.
SomaLogic (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nucleobases comprising DNA and RNA aptamers provide considerably less chemical diversity than protein-based ligands, limiting their versatility. The introduction of novel functional groups at just one of the four bases in modified aptamers has recently led to dramatic improvement in the success rate of identifying nucleic acid ligands to protein targets. Here we explore the benefits of additional enhancement in physicochemical diversity by selecting modified DNA aptamers that contain amino-acid-like modifications on both pyrimidine bases. Using proprotein convertase subtilisin/kexin type 9 as a representative protein target, we identify specific pairwise combinations of modifications that result in higher affinity, metabolic stability, and inhibitory potency compared with aptamers with single modifications. Such doubly modified aptamers are also more likely to be encoded in shorter sequences and occupy nonoverlapping epitopes more frequently than aptamers with single modifications. These highly modified DNA aptamers have broad utility in research, diagnostic, and therapeutic applications.

Indexed as

Aptamers, NucleotideSELEX Aptamer TechniqueCell Line, TumorDeoxyribonucleasesGene LibraryHumansLigandsPCSK9 InhibitorsProprotein Convertase 9Aptamers, NucleotideDeoxyribonucleasesLigandsPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9modified aptamerPCSK9PSMASELEXSOMAmer

Identifiers

PMID28265062
PMCPMC5358403
OpenAlexW2591787342

What OpenQuestion holds

Textmetadata
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.