| Literature DB >> 27777026 |
William A Cantara1, Erik D Olson1, Karin Musier-Forsyth2.
Abstract
In addition to their role in correctly attaching specific amino acids to cognate tRNAs, aminoacyl-tRNA synthetases (aaRS) have been found to possess many alternative functions and often bind to and act on other nucleic acids. In contrast to the well-defined 3D structure of tRNA, the structures of many of the other RNAs recognized by aaRSs have not been solved. Despite advances in the use of X-ray crystallography (XRC), nuclear magnetic resonance (NMR) spectroscopy and cryo-electron microscopy (cryo-EM) for structural characterization of biomolecules, significant challenges to solving RNA structures still exist. Recently, small-angle X-ray scattering (SAXS) has been increasingly employed to characterize the 3D structures of RNAs and RNA-protein complexes. SAXS is capable of providing low-resolution tertiary structure information under physiological conditions and with less intensive sample preparation and data analysis requirements than XRC, NMR and cryo-EM. In this article, we describe best practices involved in the process of RNA and RNA-protein sample preparation, SAXS data collection, data analysis, and structural model building.Entities:
Keywords: Aminoacyl-tRNA synthetase; Native PAGE; RNA structure; SAXS; Size-exclusion chromatography; tRNA-like structures
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Year: 2016 PMID: 27777026 PMCID: PMC5253320 DOI: 10.1016/j.ymeth.2016.10.008
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608