Molecular choreography: Unveiling the dynamic landscape of type IIA DNA topoisomerases before T-segment passage through all-atom simulations

Int J Biol Macromol. 2024 Jun;269(Pt 2):131991. doi: 10.1016/j.ijbiomac.2024.131991. Epub 2024 May 5.

Abstract

Type IIA DNA topoisomerases are molecular nanomachines responsible for controlling topological states of DNA molecules. Here, we explore the dynamic landscape of yeast topoisomerase IIA during key stages of its catalytic cycle, focusing in particular on the events preceding the passage of the T-segment. To this end, we generated six configurations of fully catalytic yeast topo IIA, strategically inserted a T-segment into the N-gate in relevant configurations, and performed all-atom simulations. The essential motion of topo IIA protein dimer was characterized by rotational gyrating-like movement together with sliding motion within the DNA-gate. Both appear to be inherent properties of the enzyme and an inbuilt feature that allows passage of the T-segment through the cleaved G-segment. Coupled dynamics of the N-gate and DNA-gate residues may be particularly important for controlled and smooth passage of the T-segment and consequently the prevention of DNA double-strand breaks. QTK loop residue Lys367, which interacts with ATP and ADP molecules, is involved in regulating the size and stability of the N-gate. The unveiled features of the simulated configurations provide insights into the catalytic cycle of type IIA topoisomerases and elucidate the molecular choreography governing their ability to modulate the topological states of DNA topology.

Keywords: Catalytic cycle; Molecular dynamics; Molecular simulations; T-segment; Type IIA DNA topoisomerase.

MeSH terms

  • DNA / chemistry
  • DNA / metabolism
  • DNA Topoisomerases, Type II* / chemistry
  • DNA Topoisomerases, Type II* / metabolism
  • Molecular Dynamics Simulation*
  • Nucleic Acid Conformation
  • Protein Multimerization
  • Saccharomyces cerevisiae / enzymology

Substances

  • DNA Topoisomerases, Type II
  • DNA