Abstract

With the increasing trend of using microcrystals and intense microbeams at synchrotron X-ray beamlines, radiation damage becomes a more pressing problem. Theoretical calculations show that the photoelectrons that primarily cause damage can escape microcrystals. This effect would become more pronounced with decreasing crystal size as well as at higher energies. To prove this effect, data from cryocooled lysozyme crystals of dimensions 5 × 3 × 3 and 20 × 8 × 8 µm mounted on cryo-transmission electron microscopy (cryo-TEM) grids were collected at 13.5 and 20.1 keV using a PILATUS CdTe 2M detector, which has a similar quantum efficiency at both energies. Accurate absorbed doses were calculated through the direct measurement of individual crystal sizes using scanning electron microscopy after the experiment and characterization of the X-ray microbeam. The crystal lifetime was then quantified based on the D 1/2 metric. Inthis first systematic study, a longer crystal lifetime for smaller crystals was observed and crystal lifetime increased at higher X-ray energies, supporting the theoretical predictions of photoelectron escape. The use of detector technologies specifically optimized for data collection at energies above 20 keV allows the theoretically predicted photoelectron escape to be quantified and exploited, guiding future beamline-design choices.

Highlights

  • With the advances in X-ray focusing techniques and increasing brilliance of the late third and the new fourth generations of synchrotrons, highly intense microbeams have become widely available (Yamamoto et al, 2017)

  • Higher flux densities imply that more energy is deposited in the protein crystal, making radiation damage an even more pressing problem

  • This is the first systematic study showing the effect of photoelectron escape in microcrystals

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Summary

Introduction

With the advances in X-ray focusing techniques and increasing brilliance of the late third and the new fourth generations of synchrotrons, highly intense microbeams have become widely available (Yamamoto et al, 2017). When an X-ray photon is absorbed by a protein crystal, the most likely event is the generation of a photoelectron with a similar energy. This photoelectron is scattered inelastically within the crystal and produces secondary lower energy electrons, causing further damage (Ravelli & Garman, 2006). By simulating the paths of photoelectrons, Nave & Hill (2005) showed that a significant fraction of the high-energy photoelectrons escape the crystal before causing further damage if the crystal size is less than 10 mm and the surrounding material is minimized

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