TY - JOUR
T1 - Mitigation of X-ray damage in macromolecular crystallography by submicrometre line focusing
AU - Finfrock, Y. Zou
AU - Stern, Edward A.
AU - Alkire, R. W.
AU - Kas, Joshua J.
AU - Evans-Lutterodt, Kenneth
AU - Stein, Aaron
AU - Duke, Norma
AU - Lazarski, Krzysztof
AU - Joachimiak, Andrzej
PY - 2013/8
Y1 - 2013/8
N2 - Reported here are measurements of the penetration depth and spatial distribution of photoelectron (PE) damage excited by 18.6 keV X-ray photons in a lysozyme crystal with a vertical submicrometre line-focus beam of 0.7 μm full-width half-maximum (FWHM). The experimental results determined that the penetration depth of PEs is 5 ± 0.5 μm with a monotonically decreasing spatial distribution shape, resulting in mitigation of diffraction signal damage. This does not agree with previous theoretical predication that the mitigation of damage requires a peak of damage outside the focus. A new improved calculation provides some qualitative agreement with the experimental results, but significant errors still remain. The mitigation of radiation damage by line focusing was measured experimentally by comparing the damage in the X-ray-irradiated regions of the submicrometre focus with the large-beam case under conditions of equal exposure and equal volumes of the protein crystal, and a mitigation factor of 4.4 ± 0.4 was determined. The mitigation of radiation damage is caused by spatial separation of the dominant PE radiation-damage component from the crystal region of the line-focus beam that contributes the diffraction signal. The diffraction signal is generated by coherent scattering of incident X-rays (which introduces no damage), while the overwhelming proportion of damage is caused by PE emission as X-ray photons are absorbed.
AB - Reported here are measurements of the penetration depth and spatial distribution of photoelectron (PE) damage excited by 18.6 keV X-ray photons in a lysozyme crystal with a vertical submicrometre line-focus beam of 0.7 μm full-width half-maximum (FWHM). The experimental results determined that the penetration depth of PEs is 5 ± 0.5 μm with a monotonically decreasing spatial distribution shape, resulting in mitigation of diffraction signal damage. This does not agree with previous theoretical predication that the mitigation of damage requires a peak of damage outside the focus. A new improved calculation provides some qualitative agreement with the experimental results, but significant errors still remain. The mitigation of radiation damage by line focusing was measured experimentally by comparing the damage in the X-ray-irradiated regions of the submicrometre focus with the large-beam case under conditions of equal exposure and equal volumes of the protein crystal, and a mitigation factor of 4.4 ± 0.4 was determined. The mitigation of radiation damage is caused by spatial separation of the dominant PE radiation-damage component from the crystal region of the line-focus beam that contributes the diffraction signal. The diffraction signal is generated by coherent scattering of incident X-rays (which introduces no damage), while the overwhelming proportion of damage is caused by PE emission as X-ray photons are absorbed.
KW - X-ray damage mitigation
KW - photoelectrons
KW - submicrometre line focusing
UR - http://www.scopus.com/inward/record.url?scp=84881266023&partnerID=8YFLogxK
U2 - 10.1107/s0907444913009335
DO - 10.1107/s0907444913009335
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C2 - 23897469
AN - SCOPUS:84881266023
SN - 0907-4449
VL - 69
SP - 1463
EP - 1469
JO - Acta Crystallographica Section D: Biological Crystallography
JF - Acta Crystallographica Section D: Biological Crystallography
IS - 8
ER -