Localized reconstruction of subunits from electron cryomicroscopy images of macromolecular complexes.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26534841.
- Also identified by DOI 10.1038/ncomms9843 and PMC identifier 4667630.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Electron cryomicroscopy can yield near-atomic resolution structures of highly ordered macromolecular complexes. Often however some subunits bind in a flexible manner, have different symmetry from the rest of the complex, or are present in sub-stoichiometric amounts, limiting the attainable resolution. Here we report a general method for the localized three-dimensional reconstruction of such subunits. After determining the particle orientations, local areas corresponding to the subunits can be extracted and treated as single particles. We demonstrate the method using three examples including a flexible assembly and complexes harbouring subunits with either partial occupancy or mismatched symmetry. Most notably, the method allows accurate fitting of the monomeric RNA-dependent RNA polymerase bound at the threefold axis of symmetry inside a viral capsid, revealing for the first time its exact orientation and interactions with the capsid proteins. Localized reconstruction is expected to provide novel biological insights in a range of challenging biological systems.
Medical subject headings
- Capsid Proteins
- Cryoelectron Microscopy
- Macromolecular Substances
- Protein Subunits
- RNA-Dependent RNA Polymerase