| Literature DB >> 20056148 |
Mirabela Rusu1, Stefan Birmanns.
Abstract
A structural characterization of multi-component cellular assemblies is essential to explain the mechanisms governing biological function. Macromolecular architectures may be revealed by integrating information collected from various biophysical sources - for instance, by interpreting low-resolution electron cryomicroscopy reconstructions in relation to the crystal structures of the constituent fragments. A simultaneous registration of multiple components is beneficial when building atomic models as it introduces additional spatial constraints to facilitate the native placement inside the map. The high-dimensional nature of such a search problem prevents the exhaustive exploration of all possible solutions. Here we introduce a novel method based on genetic algorithms, for the efficient exploration of the multi-body registration search space. The classic scheme of a genetic algorithm was enhanced with new genetic operations, tabu search and parallel computing strategies and validated on a benchmark of synthetic and experimental cryo-EM datasets. Even at a low level of detail, for example 35-40 A, the technique successfully registered multiple component biomolecules, measuring accuracies within one order of magnitude of the nominal resolutions of the maps. The algorithm was implemented using the Sculptor molecular modeling framework, which also provides a user-friendly graphical interface and enables an instantaneous, visual exploration of intermediate solutions. (c) 2009 Elsevier Inc. All rights reserved.Entities:
Keywords: cryo-EM; cryo-electron microscopy; genetic algorithms; macromolecular assembly; multi-body registration; multi-resolution modeling; multicomponent; simultaneous registration; tabu search
Mesh:
Substances:
Year: 2010 PMID: 20056148 PMCID: PMC2872094 DOI: 10.1016/j.jsb.2009.12.028
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867