Evidence map›Paper›PMID 30820532›Full record

ArticleNucleic acids research2019

Submolecular dissection reveals strong and specific binding of polyamide-pyridostatin conjugates to human telomere interface.

Shankar Mandal, Yusuke Kawamoto, Zhizhou Yue, Kaori Hashiya, Yunxi Cui, Toshikazu Bando, Shankar Pandey, Mohammed Enamul Hoque, Mohammad Akter Hossain, Hiroshi Sugiyama and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  5. Article
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  7. Mechanical Stability of DNA Corona Phase on Gold Nanospheres.Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
  8. Article
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  11. Review
  12. Article
  13. Article
  14. Duplex formation in a G-quadruplex bulge.Nucleic acids research · 2020
    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

11 authors at 3 institutions in 3 countries.

Shankar MandalDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Yusuke KawamotoDepartment of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Zhizhou YueDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Kaori HashiyaDepartment of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Yunxi CuiDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Toshikazu BandoDepartment of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Shankar PandeyDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Mohammed Enamul HoqueDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Mohammad Akter HossainDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Hiroshi SugiyamaDepartment of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Hanbin MaoDepartment of Chemistry & Biochemistry, Kent State University, Kent, OH 44242, USA.
Kent State University · USKyoto University · JPNankai University · CN

Funding

Specific Recognition of G-quadruplexesR01CA236350 · NCI · KENT STATE UNIVERSITY · PI MAO, HANBIN · 2018 to 2022
$1.6M
NCI NIH HHS R01 CA236350
6 · The paper itself

Abstract

To modulate biological functions, G-quadruplexes in genome are often non-specifically targeted by small molecules. Here, specificity is increased by targeting both G-quadruplex and its flanking duplex DNA in a naturally occurring dsDNA-ssDNA telomere interface using polyamide (PA) and pyridostatin (PDS) conjugates (PA-PDS). We innovated a single-molecule assay in which dissociation constant (Kd) of the conjugate can be separately evaluated from the binding of either PA or PDS. We found Kd of 0.8 nM for PA-PDS, which is much lower than PDS (Kd ∼ 450 nM) or PA (Kd ∼ 35 nM). Functional assays further indicated that the PA-PDS conjugate stopped the replication of a DNA polymerase more efficiently than PA or PDS. Our results not only established a new method to dissect multivalent binding into actions of individual monovalent components, they also demonstrated a strong and specific G-quadruplex targeting strategy by conjugating highly specific duplex-binding molecules with potent quadruplex ligands.

Indexed as

AminoquinolinesBase SequenceDNAHumansNylonsPicolinic AcidsSubstrate SpecificityTelomereAminoquinolinesDNANylonsPicolinic Acidspyridostatin

Identifiers

PMID30820532
PMCPMC6468309
OpenAlexW2920228638

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.