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An on-demand, drop-on-drop method for studying enzyme catalysis by serial crystallography
- Butryn, Agata;
- Simon, Philipp S;
- Aller, Pierre;
- Hinchliffe, Philip;
- Massad, Ramzi N;
- Leen, Gabriel;
- Tooke, Catherine L;
- Bogacz, Isabel;
- Kim, In-Sik;
- Bhowmick, Asmit;
- Brewster, Aaron S;
- Devenish, Nicholas E;
- Brem, Jürgen;
- Kamps, Jos JAG;
- Lang, Pauline A;
- Rabe, Patrick;
- Axford, Danny;
- Beale, John H;
- Davy, Bradley;
- Ebrahim, Ali;
- Orlans, Julien;
- Storm, Selina LS;
- Zhou, Tiankun;
- Owada, Shigeki;
- Tanaka, Rie;
- Tono, Kensuke;
- Evans, Gwyndaf;
- Owen, Robin L;
- Houle, Frances A;
- Sauter, Nicholas K;
- Schofield, Christopher J;
- Spencer, James;
- Yachandra, Vittal K;
- Yano, Junko;
- Kern, Jan F;
- Orville, Allen M
- et al.
Published Web Location
https://doi.org/10.1038/s41467-021-24757-7Abstract
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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