Type II topoisomerase substrate geometry revealed through combined experiment and computation
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Type II topoisomerases (topo IIs) are essential enzymes that regulate DNA topology through a strand-passage mechanism in which a duplex DNA (transfer-segment) is passed through a transiently cleaved second duplex DNA (gate-segment). Biochemical and structural approaches have revealed critical details of the binding and cleavage of the gate-segment DNA. However, capture of the transfer-segment DNA has proven more difficult to resolve due to the transient nature of the interaction. Nonetheless, selection of the transfer segment with a specific conformation or orientation relative to the gate segment is predicted to govern aspects of topo II activity, including chiral discrimination and the ability to reduce topological complexity below equilibrium. To determine the conformation and orientation of the transfer-segment relative to the gate segment, we combined experimental single-molecule measurements of topo II unlinking a single DNA crossing with Brownian dynamics simulations of the DNA crossing. By correlating the unlinking rate with the geometric features of the DNA crossing, we obtain the complete three-dimensional preferred crossing geometry for strand passage. Strikingly, the preferred crossing geometries for Escherichia coli topoisomerase IV and Methanosarcina mazei topoisomerase VI are distinct and provide structural models of the DNA synapse selected for strand passage along with a mechanistic basis for their differing activities and biological functions. The approach we develop is generalizable, providing unique insights into the kinetic selection of DNA synapse structure.
Significance Statement
Type II topoisomerases resolve DNA entanglements by passing one DNA duplex through a transient break in another, but how these enzymes select the three-dimensional geometry of the DNA segments they act on has remained unresolved because the interaction is too transient to capture structurally. We developed an approach combining single-molecule measurements with Brownian dynamics simulations to determine the crossing geometry each enzyme kinetically selects. Applied to two distinct topoisomerases, this approach revealed different preferred geometries that explain long-standing differences in how these enzymes sense DNA handedness and challenge a leading model for how topoisomerases simplify DNA tangles beyond what thermodynamics alone would predict. This kinetics-based strategy is broadly applicable to other enzymes that resolve DNA or RNA synapses.
