Photolyases, a ubiquitous class of flavoproteins, use blue light to repair DNA photolesions. In this work, we determined the structural mechanism of the photolyase-catalyzed repair of a cyclobutane pyrimidine dimer (CPD) lesion using time-resolved serial femtosecond crystallography (TR-SFX). We obtained 18 snapshots that show time-dependent changes in four reaction loci. We used these results to create a movie that depicts the repair of CPD lesions in the picosecond-to-nanosecond range, followed by the recovery of the enzymatic moieties involved in catalysis, completing the formation of the fully reduced enzyme-product complex at 500 nanoseconds. Finally, back-flip intermediates of the thymine bases to reanneal the DNA were captured at 25 to 200 microseconds. Our data cover the complete molecular mechanism of a photolyase and, importantly, its chemistry and enzymatic catalysis at work across a wide timescale and at atomic resolution.
Archaeal Proteins , DNA Repair , Deoxyribodipyrimidine Photo-Lyase , Methanosarcina , Pyrimidine Dimers , Archaeal Proteins/chemistry , Catalysis , Crystallography/methods , Deoxyribodipyrimidine Photo-Lyase/chemistry , DNA/chemistry , DNA/radiation effects , Methanosarcina/enzymology , Protein Conformation , Pyrimidine Dimers/chemistry , Ultraviolet Rays
