- Molecular replacement
Molecular replacement (or MR) is a method of solving the phase problem in X-ray crystallography. MR relies upon the existence of a previously solved protein structure which is homologous (similar) to our unknown structure from which the diffraction data is derived.
The first goal of the crystallographer is to obtain an electron density map, density being related with diffracted wave as follows:
With usual detectors the intensity is being measured, so all the information about phase (Φ) is lost. Then, in the absence of phases (Φ), we are unable to complete the shown Fourier transform relating the experimental data from X-ray crystallography (in reciprocal space) to real-space electron density, into which the atomic model is built. MR tries to find the model which fits best experimental intensities among known structures.
Principles of Patterson-based molecular replacement
However, we can derive a Patterson map, which is an interatomic vector map created by squaring the structure factor amplitudes and setting all phases to zero. This vector map contains a peak for each atom related to every other atom, with a large peak at 0,0,0, where vectors relating atoms to themselves "pile up". Such a map is far too noisy to derive any high resolution structural information—however if we generate Patterson maps for the data derived from our unknown structure, and from the structure of a previously solved homologue, in the correct orientation and position within the unit cell, the two Patterson maps should be closely correlated. This principle lies at the heart of MR, and can allow us to infer information about the orientation and location of an unknown molecule with its unit cell.
In the rotation function, our unknown Patterson map is compared to Patterson maps derived from our known homologue structure in different orientations. Historically r-factors and/or correlation coefficients were used to score the rotation function, however, modern programs use maximum likelihood-based algorthims. The highest correlation (and therefore scores) are obtained when the two structures (known and unknown) are in similar orientation(s)—these can then be output in Euler angles or spherical polar angles.
In the translation function, the now correctly oriented known model can be correctly positioned by translating it to the correct co-ordinates within the asymmetric unit. This is accomplished by moving the model, calculating a new Patterson map, and comparing it to the unknown-derived patterson map. This brute-force search is computationally expensive and fast translation functions are now more commonly used. Positions with high correlations are output in Cartesian coordinates.
The next step
Following this, we should have correctly oriented and translated phasing models, from which we can derive phases which are (hopefully) accurate enough to derive electron density maps. These can be used to build and refine an atomic model of our unknown structure.
- ^ Ch 10 in "Principles of Protein X-ray Crystallography", by Jan Drenth (2nd Edn.) Springer, 1999
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