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Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2. / Davletgildeeva, Anastasiia T; Tyugashev, Timofey E; Zhao, Mingxing и др.

в: Cells, Том 12, № 14, 1839, 13.07.2023.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Davletgildeeva, AT, Tyugashev, TE, Zhao, M, Kuznetsov, NA, Ishchenko, AA, Saparbaev, M & Kuznetsova, AA 2023, 'Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2', Cells, Том. 12, № 14, 1839. https://doi.org/10.3390/cells12141839

APA

Davletgildeeva, A. T., Tyugashev, T. E., Zhao, M., Kuznetsov, N. A., Ishchenko, A. A., Saparbaev, M., & Kuznetsova, A. A. (2023). Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2. Cells, 12(14), [1839]. https://doi.org/10.3390/cells12141839

Vancouver

Davletgildeeva AT, Tyugashev TE, Zhao M, Kuznetsov NA, Ishchenko AA, Saparbaev M и др. Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2. Cells. 2023 июль 13;12(14):1839. doi: 10.3390/cells12141839

Author

Davletgildeeva, Anastasiia T ; Tyugashev, Timofey E ; Zhao, Mingxing и др. / Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2. в: Cells. 2023 ; Том 12, № 14.

BibTeX

@article{84ac2fc029f445a78b415f0c7dabe7df,
title = "Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2",
abstract = "Human Fe(II)/α-ketoglutarate-dependent dioxygenase ABH2 plays a crucial role in the direct reversal repair of nonbulky alkyl lesions in DNA nucleobases, e.g., N1-methyladenine (m1A), N3-methylcytosine (m3C), and some etheno derivatives. Moreover, ABH2 is capable of a less efficient oxidation of an epigenetic DNA mark called 5-methylcytosine (m5C), which typically is a specific target of DNA dioxygenases from the TET family. In this study, to elucidate the mechanism of the substrate specificity of ABH2, we investigated the role of several active-site amino acid residues. Functional mapping of the lesion-binding pocket was performed through the analysis of the functions of Tyr122, Ile168, and Asp173 in the damaged base recognition mechanism. Interactions of wild-type ABH2, or its mutants Y122A, I168A, or D173A, with damaged DNA containing the methylated base m1A or m3C or the epigenetic marker m5C were analyzed by molecular dynamics simulations and kinetic assays. Comparative analysis of the enzymes revealed an effect of the substitutions on DNA binding and on catalytic activity. Obtained data clearly demonstrate the effect of the tested amino acid residues on the catalytic activity of the enzymes rather than the DNA-binding ability. Taken together, these data shed light on the molecular and kinetic consequences of the substitution of active-site residues for the mechanism of the substrate recognition.",
author = "Davletgildeeva, {Anastasiia T} and Tyugashev, {Timofey E} and Mingxing Zhao and Kuznetsov, {Nikita A} and Ishchenko, {Alexander A} and Murat Saparbaev and Kuznetsova, {Aleksandra A}",
note = "Funding: This work was partially supported by the Russian Federal Ministry of Science and Higher Education (project no. 121031300041-4 for N.A.K.), by Electricit{\'e} de France (grant nos. RB 2020-02 and RB 2021-05 to M.S.), by the French National Research Agency (grant no. ANR-18-CE44-0008 to A.A.I.), and Fondation ARC (grant no. PJA-2021060003796 to A.A.I.). The part of the work involving the analysis of the ABH2 conformational dynamics and activity was specifically funded by the Russian Science Foundation grant no. 21-14-00018.",
year = "2023",
month = jul,
day = "13",
doi = "10.3390/cells12141839",
language = "English",
volume = "12",
journal = "Cells",
issn = "2073-4409",
publisher = "MDPI AG",
number = "14",

}

RIS

TY - JOUR

T1 - Individual Contributions of Amido Acid Residues Tyr122, Ile168, and Asp173 to the Activity and Substrate Specificity of Human DNA Dioxygenase ABH2

AU - Davletgildeeva, Anastasiia T

AU - Tyugashev, Timofey E

AU - Zhao, Mingxing

AU - Kuznetsov, Nikita A

AU - Ishchenko, Alexander A

AU - Saparbaev, Murat

AU - Kuznetsova, Aleksandra A

N1 - Funding: This work was partially supported by the Russian Federal Ministry of Science and Higher Education (project no. 121031300041-4 for N.A.K.), by Electricité de France (grant nos. RB 2020-02 and RB 2021-05 to M.S.), by the French National Research Agency (grant no. ANR-18-CE44-0008 to A.A.I.), and Fondation ARC (grant no. PJA-2021060003796 to A.A.I.). The part of the work involving the analysis of the ABH2 conformational dynamics and activity was specifically funded by the Russian Science Foundation grant no. 21-14-00018.

PY - 2023/7/13

Y1 - 2023/7/13

N2 - Human Fe(II)/α-ketoglutarate-dependent dioxygenase ABH2 plays a crucial role in the direct reversal repair of nonbulky alkyl lesions in DNA nucleobases, e.g., N1-methyladenine (m1A), N3-methylcytosine (m3C), and some etheno derivatives. Moreover, ABH2 is capable of a less efficient oxidation of an epigenetic DNA mark called 5-methylcytosine (m5C), which typically is a specific target of DNA dioxygenases from the TET family. In this study, to elucidate the mechanism of the substrate specificity of ABH2, we investigated the role of several active-site amino acid residues. Functional mapping of the lesion-binding pocket was performed through the analysis of the functions of Tyr122, Ile168, and Asp173 in the damaged base recognition mechanism. Interactions of wild-type ABH2, or its mutants Y122A, I168A, or D173A, with damaged DNA containing the methylated base m1A or m3C or the epigenetic marker m5C were analyzed by molecular dynamics simulations and kinetic assays. Comparative analysis of the enzymes revealed an effect of the substitutions on DNA binding and on catalytic activity. Obtained data clearly demonstrate the effect of the tested amino acid residues on the catalytic activity of the enzymes rather than the DNA-binding ability. Taken together, these data shed light on the molecular and kinetic consequences of the substitution of active-site residues for the mechanism of the substrate recognition.

AB - Human Fe(II)/α-ketoglutarate-dependent dioxygenase ABH2 plays a crucial role in the direct reversal repair of nonbulky alkyl lesions in DNA nucleobases, e.g., N1-methyladenine (m1A), N3-methylcytosine (m3C), and some etheno derivatives. Moreover, ABH2 is capable of a less efficient oxidation of an epigenetic DNA mark called 5-methylcytosine (m5C), which typically is a specific target of DNA dioxygenases from the TET family. In this study, to elucidate the mechanism of the substrate specificity of ABH2, we investigated the role of several active-site amino acid residues. Functional mapping of the lesion-binding pocket was performed through the analysis of the functions of Tyr122, Ile168, and Asp173 in the damaged base recognition mechanism. Interactions of wild-type ABH2, or its mutants Y122A, I168A, or D173A, with damaged DNA containing the methylated base m1A or m3C or the epigenetic marker m5C were analyzed by molecular dynamics simulations and kinetic assays. Comparative analysis of the enzymes revealed an effect of the substitutions on DNA binding and on catalytic activity. Obtained data clearly demonstrate the effect of the tested amino acid residues on the catalytic activity of the enzymes rather than the DNA-binding ability. Taken together, these data shed light on the molecular and kinetic consequences of the substitution of active-site residues for the mechanism of the substrate recognition.

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85165866712&origin=inward&txGid=889c98be670862bcfd5b56e46b5d8cb2

U2 - 10.3390/cells12141839

DO - 10.3390/cells12141839

M3 - Article

C2 - 37508504

VL - 12

JO - Cells

JF - Cells

SN - 2073-4409

IS - 14

M1 - 1839

ER -

ID: 53250473