International
Tables for
Crystallography
Volume B
Reciprocal space
Edited by U. Shmueli

International Tables for Crystallography (2006). Vol. B. ch. 2.4, p. 275   | 1 | 2 |

Section 2.4.5.2. Anomalous scattering of synchrotron radiation

M. Vijayana* and S. Ramaseshanb

a Molecular Biophysics Unit, Indian Institute of Science, Bangalore 560 012, India, and bRaman Research Institute, Bangalore 560 080, India
Correspondence e-mail:  mv@mbu.iisc.ernet.in

2.4.5.2. Anomalous scattering of synchrotron radiation

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The most significant development in recent years in relation to anomalous scattering of X-rays has been the advent of synchrotron radiation (Helliwell, 1984[link]). The advantage of using synchrotron radiation for making anomalous-scattering measurements essentially arises out of the tunability of the wavelength. Unlike the characteristic radiation from conventional X-ray sources, synchrotron radiation has a smooth spectrum and the wavelength to be used can be finely selected. Accurate measurements have shown that values in the neighbourhood of 30 electrons could be obtained in favourable cases for f′ and f″ (Templeton, Templeton, Phillips & Hodgson, 1980[link]; Templeton, Templeton & Phizackerley, 1980[link]; Templeton et al., 1982[link]). Schemes for the optimization of the wavelengths to be used have also been suggested (Narayan & Ramaseshan, 1981[link]). Interestingly, the anomalous differences obtainable using synchrotron radiation are comparable in magnitude to the isomorphous differences normally encountered in protein crystallography. Thus, the use of anomalous scattering at several wavelengths would obviously eliminate the need for employing many heavy-atom derivatives. The application of anomalous scattering of synchrotron radiation for macromolecular structure analysis began to yield encouraging results in the 1980s (Helliwell, 1985[link]). Intensity measurements from macromolecular X-ray diffraction patterns using synchrotron radiation at first relied primarily upon oscillation photography (Arndt & Wonacott, 1977[link]). This method is not particularly suitable for accurately evaluating anomalous differences. Much higher levels of accuracy began to be achieved with the use of position-sensitive detectors (Arndt, 1986[link]). Anomalous scattering, in combination with such detectors, has developed into a major tool in macromolecular crystallography (see IT F , 2001[link]).

References

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