Refinement of protein structures by iterative comparative modeling and cryoEM density fitting

We developed a method for structure characterization of assembly components by iterative comparative protein structure modeling and fitting into cryo-electron microscopy (cryoEM) density maps. Specifically, we calculate a comparative model of a given component by considering many alternative alignments between the target sequence and a related template structure while optimizing the fit of a model into the corresponding density map. The method relies on the previously developed Moulder protocol that iterates over alignment, model building, and model assessment. The protocol was benchmarked using 20 varied target-template pairs of known structures with less than 30% sequence identity and corresponding simulated density maps at resolutions from 5 angstrom to 25 angstrom. Relative to the models based on the best existing sequence profile alignment methods, the percentage of C-alpha atoms that are within 5 angstrom of the corresponding C-alpha atoms in the superposed native structure increases on average from 52% to 66%, which is half-way between the starting models and the models from the best possible alignments (82%). The test also reveals that despite the improvements in the accuracy of the fitness function, this function is still the bottleneck in reducing the remaining errors. To demonstrate the usefulness of the protocol, we applied it to the upper domain of the P8 capsid protein of rice dwarf virus that has been studied by cryoEM at 6.8 angstrom. The C-alpha root-mean-square deviation of the model based on the remotely related template, bluetongue virus VP7, improved from 8.7 angstrom to 6.0 angstrom, while the best possible model has a C-alpha RMSD value of 5.3 angstrom. Moreover, the resulting model fits better into the cryoEM density map than the initial template structure. The method is being implemented in our program MODELLER for protein structure modeling by satisfaction of spatial restraints and will be applicable to the rapidly increasing number of cryoEM density maps of macromolecular assemblies. (c) 2006 Elsevier Ltd. All rights reserved.