Evidence map›Paper›PMID 37686447›Full record

ArticleInternational journal of molecular sciences2023

Non-Covalent Interactions between dUTP C5-Substituents and DNA Polymerase Decrease PCR Efficiency.

Olga A Zasedateleva, Sergey A Surzhikov, Viktoriya E Kuznetsova, Valeriy E Shershov, Victor E Barsky, Alexander S Zasedatelev, Alexander V Chudinov

Abstract read
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Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Olga A ZasedatelevaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.ORCID 0009-0008-3461-8876
Sergey A SurzhikovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.
Viktoriya E KuznetsovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.
Valeriy E ShershovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.
Victor E BarskyEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.
Alexander S ZasedatelevEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.
Alexander V ChudinovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov Street, 119991 Moscow, Russia.

Funding

Russian Science Foundation 20-14-00287
6 · The paper itself

Abstract

The approach based on molecular modeling was developed to study dNTP derivatives characterized by new polymerase-specific properties. For this purpose, the relative efficiency of PCR amplification with modified dUTPs was studied using Taq, Tth, Pfu, Vent, Deep Vent, Vent (exo-), and Deep Vent (exo-) DNA polymerases. The efficiency of PCR amplification with modified dUTPs was compared with the results of molecular modeling using the known 3D structures of KlenTaq polymerase-DNA-dNTP complexes. The dUTPs were C5-modified with bulky functional groups (the Cy5 dye analogs) or lighter aromatic groups. Comparing the experimental data and the results of molecular modeling revealed the decrease in PCR efficiency in the presence of modified dUTPs with an increase in the number of non-covalent bonds between the substituents and the DNA polymerase (about 15% decrease per one extra non-covalent bond). Generalization of the revealed patterns to all the studied polymerases of the A and B families is discussed herein. The number of non-covalent bonds between the substituents and polymerase amino acid residues is proposed to be a potentially variable parameter for regulating enzyme activity.

Indexed as

Amino AcidsDNA-Directed DNA PolymeraseDietary FiberHumansNucleotidesPolymerase Chain ReactionAmino AcidsDietary FiberDNA-Directed DNA PolymeraseNucleotidesA and B family DNA polymerasesC5-modified dUTPsmolecular modelingnon-covalent interactionsPCR amplificationX-ray structure

Identifiers

PMID37686447
PMCPMC10487964

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