Titlebook: Structure and Dynamics of RNA; P. H. Knippenberg,C. W. Hilbers Book 1986 Springer Science+Business Media New York 1986 DNA.X-ray.acid.deve

歌唱隊

A Better Way to Make RNA for Physical Studies,methods. In addition, the variety of RNA sequences easily available for study is somewhat limited. Ideally, one would like a simple method to rapidly obtain multimilligram amounts of any RNA sequence desired. Although methods for the chemical synthesis of RNA have progressed rapidly in the past seve

使堅硬

,Mg2+ — Inner Sphere Complexes at “Ends” and “Bends” of Polynucleotides and their Potential Role as er slow exchange of ligands in the inner sphere of Mg. these complexes are localised at a given site with a relatively long lifetime, whereas outer sphere complexes are much more mobile (ion atmosphere binding). Measurements of the binding kinetics demonstrate that Mg. binds to polymers like poly(A)

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匯總

faddish

Correlation Between Crystal and Solution Structures in tRNA. Yeast tRNAPhe and tRNAAsp the Models f of yeast tRNA(Asp) (5–8). As seen in Figure 1, both molecules are folded in an L-shaped conformation, which is also found for initiator tRNAs (9,10). Since the conserved or semi-conserved residues (11) are involved in the tertiary interactions which stabilize this folding (1–10), the L-shaped struc

本能

The Solution Structures of RNA Fragments Determined by Nuclear Overhauser Enhancement Measurements,trast, relatively few studies have appeared on RNA duplexes (5–10). This is probably due to two factors, both of which arise from the presence of the 2’-hydroxyl group in RNA. First, RNA is intrinsically more difficult to synthesize than DNA as an additional reactive group has to be protected during

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anaerobic

Anticodon-Anticodon Interactions and tRNA Sequence Comparison: Approaches to Codon Recognition,ly misrepresents the complexity of the underlying processes which involve precise interactions between many proteins and nucleic acids. Although the importance of the interplay of each component of the system is not well known, it is generally recognized that two molecules play a key role: transfer

extemporaneous

Studies on 15N Labelled 5S RNA: Assignments in the Helix V Region of 5S RNA, and in the 5S/L25 Compe of ribosomal RNAs in ribosome function (for review see Noller, 1984) have stimulated renewed interest in the structural and chemical properties of RNA. Of the ribosomal RNAs only one is simple enough and small enough to lend itself to detailed physical characterization in solution, 5S RNA.

receptors

Equilibria in Ribosomal RNA Secondary Structure,As, i.e. small subunit RNA (including eukaryotic 18 S rRNA, bacterial 16 S rRNA and their mitochondrial equivalents) and large subunit rRNA (eukaryotic 28 S rRNA, bacterial 23 S rRNA and mitochondrial equivalents) can be found in a review by Noller (1984). Some references to models for the small rRN