posted on 2021-08-05, 11:54authored byAgata Butryn, Philipp S. Simon, Pierre Aller, Philip Hinchliffe, Ramzi N. Massad, Gabriel LeenGabriel Leen, Catherine L. Tooke, Isabel Bogacz, In-Sik Kim, Asmit Bhowmick, Aaron S. Brewster, Nicholas E. Devenish, Jürgen Brem, Jos J. A. G. Kamps, Pauline A. Lang, Patrick Rabe, Danny Axford, John H. Beale, Bradley Davy, Ali Ebrahim, Julien Orlans, Selina L.S. Storm, Tiankun Zhou, Shigeki Owada, Rie Tanaka, Kensuke Tono, Gwyndaf Evans, Robin L. Owen, Frances A. Houle, Nicholas K. Sauter, Christopher J. Schofield, James Spencer, Vittal K. Yachandra, Junko Yano, Jan F. Kern, Allen M. Orville
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 tem poral 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 crys tallography, 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.
History
Publisher
Nature Research
Note
peer-reviewed
Other Funding information
National Institutes of Health (NIH), Biological Sciences Research Council, Royal Society Wolfson