Single-wavelength anomalous diffraction explained

Single-wavelength anomalous diffraction (SAD) is a technique used in X-ray crystallography that facilitates the determination of the structure of proteins or other biological macromolecules by allowing the solution of the phase problem. In contrast to multi-wavelength anomalous diffraction (MAD), SAD uses a single dataset at a single appropriate wavelength.

Compared to MAD, SAD has weaker phasing power and requires density modification to resolve phase ambiguity.[1] This downside is not as important as SAD's main advantage: the minimization of time spent in the beam by the crystal, thus reducing potential radiation damage to the molecule while collecting data. SAD also allows a wider choice of heavy atoms and can be conducted without a synchrotron beamline.[1] Today, selenium-SAD is commonly used for experimental phasing due to the development of methods for selenomethionine incorporation into recombinant proteins.

SAD is sometimes called "single-wavelength anomalous dispersion", but no dispersive differences are used in this technique since the data are collected at a single wavelength.

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Notes and References

  1. Web site: Dictionary of common terms used in PHENIX . phenix-online.org . en . MAD: [...] The differences in anomalous scattering around the edge allow calculation of phase angles without the phase ambiguity present in SAD experiments, although density modification will usually still be necessary to obtain an easily interpretable map. [...] Although very powerful, MAD phasing has declined somewhat in popularity relative to SAD because of the more limited choice of heavy atoms, the difficulty of avoiding radiation damage, and the requirement for a synchrotron beamline. [...] SAD: [...] SAD is often performed with selenomethionine-incorporated protein, but any anomalously scattering atom (including sulfur, if the data are of very high quality) may be used. .