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Molecular Replacement

An approach to solving the phase problem by concentrating on phase relationships that arise through X-ray diffraction  from similar molecular components. The components can be molecular fragments related through noncrystallographic symmetry (e.g. icosahedral subunits of a virus) or a similar molecule such as a homologous protein with high sequence identity.


The technique is most commonly used in biological crystallography. Typically, an attempt is made to fit the structure under investigation (the 'target' structure) to a previously solved ('probe') structure. The probe may be a different crystal form of the same protein; or it may be a different protein with a high level of sequence identity, which correlates well with structural resemblance. As a rule of thumb, molecular replacement is often straightforward if the probe is well characterized and shares at least 40% sequence identity with the target. Rotation and transformation matrices must be applied. Patterson methods are suitable for determining the rotation function R, since intramolecular vectors are all shifted to the origin of a Patterson map. The orientational fit (i.e. the quality of the calculated rotation function) has usually been assessed by monitoring R factors or real-space correlation coefficients. Increasingly, modern  programs  use maximum likelihood based algorithms.

The translation function T is then determined to shift the now correctly orientated probe  model  to the  correct  coordinates within the asymmetric unit. Space-group symmetries can be used to help reduce the computationally intense calculations required.


Early  applications  of the technique concentrated on large virus structures with icosahedral symmetry. In the 1960s the early development of the molecular replacement technique was aimed primarily at ab initio phase determination. It was only in the 1970s, when more structures became available, that it was possible to use the technique to solve homologous structures with suitable search  models .

See also

  1. Noncrystallographic symmetry. D. M. Blow. International Tables for Crystallography (2006). Vol. F, ch. 13.1, pp. 263-268 
  2. Rossmann, M. G. & Blow, D. M. (1962). Acta Cryst. 15, 24–31The detection of sub-units within the crystallographic asymmetric unit.