On the routine use of soft X-rays in macromolecular crystallography. Part IV. Efficient determination of anomalous substructures in biomacromolecules using longer X-ray wavelengths

Christoph Mueller-Dieckmann, Santosh Panjikar, Andrea Schmidt, Simone Mueller, Jochen Kuper, Arie Geerlof, Matthias Wilmanns, Rajesh K. Singh, Paul A. Tucker, Manfred S. Weiss

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Abstract

23 Different crystal forms of 19 different biological macromolecules were examined with respect to their anomalously scattering substructures using diffraction data collected at a wavelength of 2.0 Å (6.2 keV). In more than 90% of the cases the substructure was found to contain more than just the protein S atoms. The data presented suggest that chloride, sulfate, phosphate or metal ions from the buffer or even from the purification protocol are frequently bound to the protein molecule and that these ions are often overlooked, especially if they are not bound at full occupancy. Thus, in order to fully describe the macromolecule under study, it seems desirable that any structure determination be complemented with a long-wavelength data set.

Original languageEnglish
Pages (from-to)366-380
Number of pages15
JournalActa Crystallographica Section D: Biological Crystallography
Volume63
Issue number3
DOIs
Publication statusPublished - 21 Feb 2007
Externally publishedYes

Keywords

  • Anomalous substructures
  • Soft X-rays

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