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We have developed two software packages for the processing of electron diffraction patterns acquired on a slow-scan CCD camera. Automated indexing and processing of these electron diffraction patterns is possible using a program called AUTO. To obtain a set of reliable reflections, AUTO applies a number of corrections, which are necessary due to the acquisition of the patterns with a slow-scan CCD camera. To index and process unknown lattices in electron diffraction patterns obtained from, for instance, a new protein or a new crystal form, an interactive program called EDP is available. It supports indexing in an interactive manner through a graphical user interface. Processing of the electron diffraction pattern is done using a script created by EDP. Both packages run on UNIX platforms, with EDP requiring the X Window System.

A Gatan 1024 × 1024 slow-scan charge-coupled device (CCD) camera has been interfaced to a JEOL4000EX electron cryomicroscope and explored for its usefulness in the electron crystallographic analysis of thin, glucose-embedded crystals of crotoxin complex kept at -125°C. We show that the camera allows for an on-line assessment of the crystals' crystallinity, flatness, and thickness. Intensities obtained from electron diffraction patterns acquired with the camera have been statistically analyzed and were found to be consistent with theoretically expected values. A quantitative analysis of the diffraction intensity as function of the accumulated electron dose suggests the possibility of recording up to 250 diffraction patterns with 3.5 A resolution from a single crotoxin complex crystal 128 A thick. Tilt series of 125 electron diffraction patterns with 3.5 A data acquired from a single crystal are shown to be practically feasible. The current study demonstrates for the first time the effectiveness of using a slow-scan CCD camera for electron diffraction data collection from thin protein crystals at near atomic resolution.