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Long-wavelength native-SAD phasing: opportunities and challenges.
Basu, Shibom; Olieric, Vincent; Leonarski, Filip; Matsugaki, Naohiro; Kawano, Yoshiaki; Takashi, Tomizaki; Huang, Chia-Ying; Yamada, Yusuke; Vera, Laura; Olieric, Natacha; Basquin, Jerome; Wojdyla, Justyna A; Bunk, Oliver; Diederichs, Kay; Yamamoto, Masaki; Wang, Meitian.
Afiliación
  • Basu S; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Olieric V; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Leonarski F; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Matsugaki N; Structural Biology Research Center, Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba, 305-0801, Japan.
  • Kawano Y; Advanced Photon Technology Division, RIKEN SPring-8 Center, Hyogo 679-5148, Japan.
  • Takashi T; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Huang CY; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Yamada Y; Structural Biology Research Center, Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba, 305-0801, Japan.
  • Vera L; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Olieric N; Laboratory of Biomolecular Research, Department of Biology and Chemistry, Paul Scherrer Institut, Villigen, PSI 5232, Switzerland.
  • Basquin J; Department of Biochemistry, Max Planck Institute of Biochemistry, Munich, Germany.
  • Wojdyla JA; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Bunk O; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
  • Diederichs K; Department of Biology, University of Konstanz, Konstanz, 78457, Germany.
  • Yamamoto M; Advanced Photon Technology Division, RIKEN SPring-8 Center, Hyogo 679-5148, Japan.
  • Wang M; Swiss Light Source, Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.
IUCrJ ; 6(Pt 3): 373-386, 2019 May 01.
Article en En | MEDLINE | ID: mdl-31098019
ABSTRACT
Native single-wavelength anomalous dispersion (SAD) is an attractive experimental phasing technique as it exploits weak anomalous signals from intrinsic light scatterers (Z < 20). The anomalous signal of sulfur in particular, is enhanced at long wavelengths, however the absorption of diffracted X-rays owing to the crystal, the sample support and air affects the recorded intensities. Thereby, the optimal measurable anomalous signals primarily depend on the counterplay of the absorption and the anomalous scattering factor at a given X-ray wavelength. Here, the benefit of using a wavelength of 2.7 over 1.9 Šis demonstrated for native-SAD phasing on a 266 kDa multiprotein-ligand tubulin complex (T2R-TTL) and is applied in the structure determination of an 86 kDa helicase Sen1 protein at beamline BL-1A of the KEK Photon Factory, Japan. Furthermore, X-ray absorption at long wavelengths was controlled by shaping a lysozyme crystal into spheres of defined thicknesses using a deep-UV laser, and a systematic comparison between wavelengths of 2.7 and 3.3 Šis reported for native SAD. The potential of laser-shaping technology and other challenges for an optimized native-SAD experiment at wavelengths >3 Šare discussed.
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