The general goal of electron transmission imaging techniques such as Electron Crystallography, Tomography or Single Particle reconstruction is to gain a 3D computer model by integrating sets of 2D data recorded by an electron microscope. The common mathematical tool that all these techniques share is the Central Section Theorem. The theorem states that the projection along the z direction of a three dimensional volume contains the same information as the central slice in the reciprocal space (z*=0) of the 3D-Fourier transform of the volume. This means that we can gain a full sampling of the Fourier Transform of the object by the projections along all spatial directions. Accordingly, the 3D reconstruction become just a Inverse Fourier transform. The theory of Electron Optics allows to some approximation the use of images recorded by a Transfer Electron Microscope (TEM) as a projection of the sample. This means that with sufficient images of samples imaged in different orientation to the electron beam, one can simulate the sample’s three dimensional density distribution.
We have seen that the Fourier transform can be used to harvest the repeating signal of the 2D crystal. But since we are dealing with 2D crystals the periodicity is limited to the x,y-plane. The crystal is ideally only formed by one layer in the vertical direction. This results in continuously distributed Fourier component in vertical direction as illustrated. The diffraction spots we have seen in 2D with the index (h,k) now become so called lattice lines (h,k,z*) where h and k still correspond to the same Miller index, but z*defines the position along the lattice line. Projections of tilted 2D crystals now produce diffraction spots, where each reflection corresponds to the lattice line h,k and height z*. The height corresponds to the intersection of the tilted plane with the lattice line h, k and thanks to the central section theorem this can be calculated from the tilt geometry of the crystal. So each recorded image produces a set of amplitude and phases with the coordinates (h,k,z*). The goal is now to densely sample the lattice lines by integrating as much data as possible with varying orientation and tilt angle. This allows us to sample the Fourier transform of our crystal to a certain degree, but due to instrumental restrictions of the TEM, where can not record an image of a any specimen tilted higher than ±70 there will always be a missing cone.
3D merging in 2dx in follows the same workflow as for 2D merging. The problem is still merging data from different images into one common data set. Therefore finding the common phase origin is the task at hand. But in contrast to 2D data where each reflection h,k and height z*=0, the amplitude and phases of a tilted sample are usually associated with a reflection at a height that is not zero. These measurements belong to a tilted plane in the 3D Fourier space, where the tilt geometry is defined by the tilt angle (TANGL) and the orientation of the lattice on that plane (TAXA). If we would now try to refine the phase origin of the tilted image data with non-tilted dataset, then the data points available for comparison would only be the one that lie on the tilt axis. Those measurements are too few to give a sufficient alignment of the tilted data. To deal with the alignment problem of the first tilted data we need to increase the range in z* direction, so that a wider region for allowed comparisons between the non-tilted and the reference data exists as illustrated. In the following steps we will show how 2DX can merge data from 2D crystals with different tilt geometry to a 3D reconstruction of your protein structure.
Tip (Backup and Synchronize): We advise you to always backup your project before you start with 3D Merging, using the script Synchronize with Backup from “Project Tools”. This script allows you to submit your project data to a different directory.
Tip (Automatically selecting the images): Also save the merged map from 2D merging with help of the Copy Merged Dataset custom script. This script allows you to copy the last merging result to any of the given 10 registers.