International
Tables for Crystallography Volume F Crystallography of biological macromolecules Edited by M. G. Rossmann and E. Arnold © International Union of Crystallography 2006 |
International Tables for Crystallography (2006). Vol. F. ch. 15.2, p. 325
Section 15.2.2.1. Parseval's theorem
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Department of Haematology, University of Cambridge, Wellcome Trust Centre for Molecular Mechanisms in Disease, CIMR, Wellcome Trust/MRC Building, Hills Road, Cambridge CB2 2XY, England |
The importance of the phase can be understood most easily in terms of Parseval's theorem, a result that is important to the understanding of many aspects of the Fourier transform and its use in crystallography. Parseval's theorem states that the mean-square value of the variable on one side of a Fourier transform is proportional to the mean-square value of the variable on the other side. Since the Fourier transform is additive, Parseval's theorem also applies to sums or differences.
If and are, for instance, the true electron density and the electron density of the model, respectively, Parseval's theorem tells us that the r.m.s. error in the electron density is proportional to the r.m.s. error in the structure factor. (The structure-factor error is a vector error in the complex plane.)
This understanding of error in electron-density maps explains why the phase is much more important than the amplitude in determining the appearance of an electron-density map. As illustrated in Fig. 15.2.2.1, a random choice of phase (from a uniform distribution of all possible phases) will generally give a larger error in the complex plane than a random choice of amplitude [from a Wilson (1949) distribution of amplitudes].
References
Wilson, A. J. C. (1949). The probability distribution of X-ray intensities. Acta Cryst. 2, 318–321.Google Scholar