Evidence map›Paper›PMID 24615810›Full record

ArticleNucleic acids research2014

Structural basis for the recognition of diastereomeric 5',8-cyclo-2'-deoxypurine lesions by the human nucleotide excision repair system.

Konstantin Kropachev, Shuang Ding, Michael A Terzidis, Annalisa Masi, Zhi Liu, Yuqin Cai, Marina Kolbanovskiy, Chryssostomos Chatgilialoglu, Suse Broyde, Nicholas E Geacintov and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 80 citations in OpenAlex.

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  12. When UDG and hAPE1 Meet Cyclopurines. How (5'Molecules (Basel, Switzerland) · 2021
    Article
  13. Review
  14. Article
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  18. Article
  19. Review
  20. DNA Oxidation and Excision Repair Pathways.International journal of molecular sciences · 2019
    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

11 authors at 2 institutions in 2 countries.

Konstantin KropachevDepartment of Chemistry New York University, 100 Washington Square East, New York, NY 10003, USA, Department of Biology, New York University, 100 Washington Square East, New York, NY 10003, USA and Istituto per la Sintesi Organica e la Fotoreattività, Consiglio Nazionale delle Ricerche, Via P. Gobetti 101, 40129 Bologna, Italy.
Shuang Ding
Michael A Terzidis
Annalisa Masi
Zhi Liu
Yuqin Cai
Marina Kolbanovskiy
Chryssostomos Chatgilialoglu
Suse Broyde
Nicholas E Geacintov
Vladimir Shafirovich
Institute of Organic Synthesis and Photoreactivity · ITNew York University · US

Funding

Carcinogen-DNA Adducts: Topology, Conformation and Repair (Renewal)R01CA028038 · NCI · NEW YORK UNIVERSITY · PI BROYDE, SUSE · 1985 to 2014
$4.7M
DNA Lesion Structures: Mutagenicity and RepairR01CA075449 · NCI · NEW YORK UNIVERSITY · PI BROYDE, SUSE · 1997 to 2015
$4.3M
Reaction pathways &products of guanine radicals in DNAR01ES011589 · NIEHS · NEW YORK UNIVERSITY · PI SHAFIROVICH, VLADIMIR · 2002 to 2014
$4.1M
Excision of Carcinogen-DNA Adducts in NucleosomesR01CA168469 · NCI · NEW YORK UNIVERSITY · PI GEACINTOV, NICHOLAS E · 2012 to 2016
$1.6M
NCI NIH HHS CA-168469NCI NIH HHS R01 CA028038NCI NIH HHS R01 CA075449NCI NIH HHS R01 CA168469NCI NIH HHS R01 CA28038NCI NIH HHS R01 CA-75449NIEHS NIH HHS R01 ES 011589NIEHS NIH HHS R01 ES011589
6 · The paper itself

Abstract

The hydroxyl radical is a powerful oxidant that generates DNA lesions including the stereoisomeric R and S 5',8-cyclo-2'-deoxyadenosine (cdA) and 5',8-cyclo-2'-deoxyguanosine (cdG) pairs that have been detected in cellular DNA. Unlike some other oxidatively generated DNA lesions, cdG and cdA are repaired by the human nucleotide excision repair (NER) apparatus. The relative NER efficiencies of all four cyclopurines were measured and compared in identical human HeLa cell extracts for the first time under identical conditions, using identical sequence contexts. The cdA and cdG lesions were excised with similar efficiencies, but the efficiencies for both 5'R cyclopurines were greater by a factor of ∼2 than for the 5'S lesions. Molecular modeling and dynamics simulations have revealed structural and energetic origins of this difference in NER-incision efficiencies. These lesions cause greater DNA backbone distortions and dynamics relative to unmodified DNA in 5'R than in 5'S stereoisomers, producing greater impairment in van der Waals stacking interaction energies in the 5'R cases. The locally impaired stacking interaction energies correlate with relative NER incision efficiencies, and explain these results on a structural basis in terms of differences in dynamic perturbations of the DNA backbone imposed by the R and S covalent 5',8 bonds.

Indexed as

DNA RepairDeoxyadenosinesDeoxyguanosineDNADNA DamageHeLa CellsHumansMolecular Dynamics SimulationNucleic Acid ConformationStereoisomerism8,5'-cyclo-2'-deoxyadenosine8,5'-cyclo-2'-deoxyguanosineDeoxyadenosinesDeoxyguanosineDNA

Identifiers

PMID24615810
PMCPMC4041128
OpenAlexW2169186429

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.