Abstract

Serial crystallography (SX) is an emerging X-ray crystallographic method for determining macromolecule structures. It can address concerns regarding the limitations of data collected by conventional crystallography techniques, which require cryogenic-temperature environments and allow crystals to accumulate radiation damage. Time-resolved SX studies using the pump-probe methodology provide useful information for understanding macromolecular mechanisms and structure fluctuation dynamics. This Special Issue deals with the serial crystallography approach using an X-ray free electron laser (XFEL) and synchrotron X-ray source, and reviews recent SX research involving synchrotron use. These reports provide insights into future serial crystallography research trends and approaches.

Highlights

  • Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

  • Serial crystallography (SX) experiments using an X-ray free electron laser (XFEL) with a short pulse width, or short time X-ray (

  • In SX data collection, if a crystal sample is stimulated with a pump, such as an optical laser or a ligand/inhibitor solution, and diffraction data are collected by exposure to X-rays after a selected time delay

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Serial crystallography (SX) experiments using an X-ray free electron laser (XFEL) with a short pulse width, or short time X-ray (

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