Radiation Damage in Macromolecular Crystallography

Methods Mol Biol. 2017:1607:467-489. doi: 10.1007/978-1-4939-7000-1_20.

Abstract

Radiation damage inflicted on macromolecular crystals during X-ray diffraction experiments remains a limiting factor for structure solution, even when samples are cooled to cryotemperatures (~100 K). Efforts to establish mitigation strategies are ongoing and various approaches, summarized below, have been investigated over the last 15 years, resulting in a deeper understanding of the physical and chemical factors affecting damage rates. The recent advent of X-ray free electron lasers permits "diffraction-before-destruction" by providing highly brilliant and short (a few tens of fs) X-ray pulses. New fourth generation synchrotron sources now coming on line with higher X-ray flux densities than those available from third generation synchrotrons will bring the issue of radiation damage once more to the fore for structural biologists.

Keywords: Absorbed dose; Cryocrystallography; Global and specific radiation damage; Radiation damage mitigation; Radicals and their scavengers; X-ray-matter interactions.

Publication types

  • Review

MeSH terms

  • Crystallization
  • Crystallography, X-Ray / methods*
  • Electrons*
  • Free Radical Scavengers / chemistry
  • Free Radicals / antagonists & inhibitors
  • Lasers
  • Macromolecular Substances / chemistry
  • Macromolecular Substances / ultrastructure*
  • Protein Conformation
  • Proteins / chemistry
  • Proteins / ultrastructure*
  • Radiation Dosage
  • Synchrotrons / instrumentation*
  • X-Rays

Substances

  • Free Radical Scavengers
  • Free Radicals
  • Macromolecular Substances
  • Proteins