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Title:Asymmetric T-segment binding and gate dynamics govern the final stages of the type IIA topoisomerase catalytic cycle
Authors:ID Stevanović, Kristina (Author)
ID Herlah, Barbara (Author)
ID Pavlin, Matic (Author)
ID Perdih, Andrej (Author)
Files:URL URL - Source URL, visit https://www.sciencedirect.com/science/article/pii/S0141813025077736
 
.pdf PDF - Presentation file, download (10,82 MB)
MD5: 40269F78600AD6441F59522FEAF7EF44
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo KI - National Institute of Chemistry
Abstract:Type IIA DNA topoisomerases are molecular nanomachines that alter DNA topology during essential cellular processes. The final steps of their catalytic cycle, after translocation of the transported (T-) segment into the C- gate, are still not fully understood. Here, we performed all-atom molecular dynamics simulations of several conformational states of Saccharomyces cerevisiae topoisomerase IIA, each with a T-segment inserted into the C- gate. Bound ATP and ADP nucleotides allosterically modulated the N-gate dynamics, likely stabilizing the dimer and preventing premature dissociation. The T-segment was asymmetrically bound and stabilized within the C- gate by positively charged residues, and this gate remained structurally rigid, highlighting its role as a retention site. The positioning of the T-segment in the C-gate allosterically influenced the G-segment to a straighter geometry that favors religation and release. Our simulations support coordinated release of DNA segments and point to a potentially important role for dynamic communication between the gates in the mechanism. These results provide new insights into the late stages of the catalytic cycle and highlight the intertwined roles of nucleotide binding, DNA topology and coupled protein domain dynamics in regulating this important enzyme.
Keywords:type IIA DNA topoisomerase, T-segment, C-gate, catalytic cycle, molecular dynamics
Publication status:Published
Publication version:Version of Record
Publication date:01.10.2025
Year of publishing:2025
Number of pages:str. 1-17
Numbering:Vol. 327, pt. 1, ǂ[article no.] ǂ147216
PID:20.500.12556/DiRROS-23648 New window
UDC:577
ISSN on article:1879-0003
DOI:10.1016/j.ijbiomac.2025.147216 New window
COBISS.SI-ID:249271555 New window
Copyright:© 2025 The Authors. Published by Elsevier B.V.
Note:Nasl. z nasl. zaslona; Opis vira z dne 17. 9. 2025;
Publication date in DiRROS:19.09.2025
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Downloads:162
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Record is a part of a journal

Title:International journal of biological macromolecules
Shortened title:Int. j. biol. macromol.
Publisher:Elsevier
ISSN:1879-0003
COBISS.SI-ID:23180805 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J1-4402
Name:Dinamični model molekulskega stroja DNA topoizomeraze tipa II in razvoj katalitičnih inhibitorjev

Funder:ARIS - Slovenian Research and Innovation Agency
Funding programme:Young Researcher Grant

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0012
Name:Molekulske simulacije, bioinformatika in načrtovanje zdravilnih učinkovin

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P2-0421
Name:Trajnostne tehnologije in krožno gospodarstvo

Funder:HPC-RIVR consortium
Project number:S24O01-17

Licences

License:CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.

Secondary language

Language:Slovenian
Keywords:biokemija, topoizomeraza IIα, DNK, molekulska dinamika


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