Type II topoisomerases modify DNA supercoiling, and crystal structures suggest that they sharply bend DNA in the process. Bacterial gyrases are a class of type II topoisomerases which can introduce negative supercoiling by creating a wrap of DNA before strand passage. Isoforms of these essential enzymes were compared to reveal whether they can bend or wrap artificially stiffened DNA. E. coli gyrase and human topoisomerase IIα were challenged with normal DNA or stiffer DNA produced by PCR reactions in which diaminopurine (DAP) replaced adenine deoxyribonucleotidetriphosphates. On single DNA molecules twisted with magnetic tweezers to create plectonemes, the rates or pauses during relaxation of positive supercoils in DAP-substituted versus normal DNA were distinct for both enzymes. Gyrase struggled to bend or perhaps open a gap in DAP-substituted DNA, and segments of wider DAP DNA may have fit poorly into the N-gate of the human topoisomerase IIα. Pauses during processive activity on both types of DNA exhibited ATP-dependence consistent with two pathways leading to the strand-passage competent state with a bent gate segment and a transfer segment trapped by an ATP-loaded and latched N-gate. However, E. coli DNA gyrase essentially failed to negatively supercoil 35% stiffer DAP DNA.
Here we describe experiments which employ magnetic tweezers and or microfluidics to manipulate single DNA molecules. We describe the use of magnetic tweezers coupled to an inverted microscope as well as the use of a magnetic tweezers setup with an upright microscope. Using a chamber prepared via soft lithography, we also describe a microfluidic device for the manipulation of individual DNA molecules. Finally, we present some past successful examples of using these approaches to elucidate unique information about protein-nucleic acid interactions.
Type II topoisomerases maintain DNA topology by regulating the level of supercoiling of chromosomes. DNA gyrase is a unique and highly conserved bacterial Type II topoisomerase which is able to introduce negative supercoils into the genome. Using magnetic-tweezers, we assessed the supercoil generation and relaxation activities of Escherichia coli and Salmonella typhimurium DNA gyrases. Our results indicate that under single-enzyme conditions and 0.6-pN tension, both enzymes relax DNA at similar rates, but Salmonella gyrase pauses more often. At high enzyme concentration and lower tensions, Salmonella gyrase introduced negative supercoils faster and to a larger extent than E. coli gyrase. Sequence and structure analyses show that most of the differences between the two enzymes are in the C-terminal domain, involved in DNA wrapping. Our ongoing single-molecule experiments to assess the DNA wrapping activities of both enzymes may reveal differences in their mechanistic properties.
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