Abstract
Electron microscopy together with single-particle image processing is an excellent method for structure determination of biological assemblies that exist in multiple identical copies. Typical assemblies contain several proteins and/or nucleic acids in a defined and reproducible arrangement. Coherent averaging of electron microscopic images of 5000-100,000 copies of these assemblies allows the determination of three-dimensional structures at ca. 1-3-nm resolution. At this intermediate resolution, it is possible to map individual subunits and thus to understand the architecture and quaternary structure of the assemblies. The intermediate resolution structural information gives a solid basis on which pseudo-atomic models of the assemblies can be modeled provided that high-resolution structures of smaller entities are known. The architecture of the assemblies, their pseudo-atomic models, and knowledge on their plasticity during function give a comprehensive understanding of large-scale structural dynamics of multicopy biological complexes. In this review, we will introduce the experimental pipeline and discuss selected examples.
| Original language | English |
|---|---|
| Title of host publication | ADVANCES IN PROTEIN CHEMISTRY AND STRUCTURAL BIOLOGY: RECENT ADVANCES IN ELECTRON CRYOMICROSCOPY, PT A |
| Place of Publication | SAN DIEGO |
| Publisher | Academic Press |
| Pages | 61-88 |
| Number of pages | 28 |
| DOIs | |
| Publication status | Published - 2010 |
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