As DNA repair enzymes are essential for preserving genome integrity, understanding their substrate interaction dynamics and the regulation of their catalytic mechanisms is crucial. Using single-molecu
Immobilized single horseradish peroxidase enzymes were observed by confocal fluorescence spectroscopy during catalysis of the oxidation reaction of the nonfluorescent dihydrorhodamine 6G substrate int
Data extracted from droplet microscopy images for all 9 frames (experiment GuGi551, Heat Shock treatment at 60 °C of Nt.BstNBI enzyme, Figure 6). To be imported in Mathematica Each element of the l
