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An on-demand, drop-on-drop method for studying enzyme catalysis by serial crystallography.

Agata ButrynPhilipp S SimonPierre AllerPhilip HinchliffeRamzi N MassadGabriel LeenCatherine L TookeIsabel BogaczIn-Sik KimAsmit BhowmickAaron S BrewsterNicholas E DevenishJürgen BremJos J A G KampsPauline A LangPatrick RabeDanny N AxfordJohn H BealeBradley DavyAli EbrahimJulien OrlansSelina L S StormTiankun ZhouShigeki OwadaRie TanakaKensuke TonoGwyndaf EvansRobin L OwenFrances A HouleNicholas K SauterChristopher J SchofieldJames SpencerVittal K YachandraJunko YanoJan F KernAllen M Orville
Published in: Nature communications (2021)
Serial femtosecond crystallography has opened up many new opportunities in structural biology. In recent years, several approaches employing light-inducible systems have emerged to enable time-resolved experiments that reveal protein dynamics at high atomic and temporal resolutions. However, very few enzymes are light-dependent, whereas macromolecules requiring ligand diffusion into an active site are ubiquitous. In this work we present a drop-on-drop sample delivery system that enables the study of enzyme-catalyzed reactions in microcrystal slurries. The system delivers ligand solutions in bursts of multiple picoliter-sized drops on top of a larger crystal-containing drop inducing turbulent mixing and transports the mixture to the X-ray interaction region with temporal resolution. We demonstrate mixing using fluorescent dyes, numerical simulations and time-resolved serial femtosecond crystallography, which show rapid ligand diffusion through microdroplets. The drop-on-drop method has the potential to be widely applicable to serial crystallography studies, particularly of enzyme reactions with small molecule substrates.
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