Non-Protein Coding RNAs (Springer Series in Biophysics) - download pdf or read online

By Sarah A. Woodson, Robert T. Batey, Nils Walter

ISBN-10: 3642089801

ISBN-13: 9783642089800

This ebook assembles chapters from specialists within the Biophysics of RNA to supply a greatly obtainable photo of the present prestige of this swiftly increasing box. The 2006 Nobel Prize in body structure or medication was once offered to the discoverers of RNA interference, highlighting only one instance of a big variety of non-protein coding RNAs. simply because non-protein coding RNAs outnumber protein coding genes in mammals and different larger eukaryotes, it really is now idea that the complexity of organisms is correlated with the fraction in their genome that encodes non-protein coding RNAs. crucial organic procedures as varied as mobile differentiation, suppression of infecting viruses and parasitic transposons, higher-level association of eukaryotic chromosomes, and gene expression itself are chanced on to principally be directed by means of non-protein coding RNAs. The biophysical examine of those RNAs employs X-ray crystallography, NMR, ensemble and unmarried molecule fluorescence spectroscopy, optical tweezers, cryo-electron microscopy, and different quantitative instruments. This rising box has began to solve the molecular underpinnings of ways RNAs satisfy their multitude of roles in maintaining mobile lifestyles. The actual and chemical figuring out of RNA biology that effects from biophysical reviews is important to our skill to harness RNAs to be used in biotechnology and human treatment, a prospect that has lately spawned a multi-billion buck undefined.

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Extra resources for Non-Protein Coding RNAs (Springer Series in Biophysics)

Sample text

As a result, hairpin formation, when examined in detail, need not follow the classical two-state kinetics. Indeed, a series of recent experiments show that the kinetics of hairpin formation in RNA or ssDNA is best described as a multi-step process (Jung and Van Orden 2006; Ma et al. 2006, 2007), thus challenging the conventional premise that small nucleic acid hairpins, fold in a two-state manner (Bloomfield et al. 2000; Tinoco et al. 2002; Turner et al. 1988). The signatures of multi-state folding/unfolding are reflected in the kinetic data of ultra fast T-jump experiments that can discern the metastable intermediates.

27 (Dima et al. 2005). This shows that 46% of the sequence, which is computed using NBP/N ≈ (1 − x)/2, constitute non-pairing regions such as bulges, loops, dangling ends, and other motifs. The bulges and loops are important structural elements that glue the independent helices together to make the RNA structures compact. 4. Finally, the folding mechanisms can be greatly altered by changing the nature of counterions which makes it necessary to consider explicitly the polyelectrolyte nature of RNA.

These structural features are summarized in the panel labeled “GNRA Definition” in Fig. 6. The positions where insertions are observed are also shown. The search also returns valuable co-variation information for each base pair in the motif. This data is summarized as 4 × 4 contingency tables for each base pair superposed on the corresponding Isostericity Matrix for that base pair type (lower left panels of Fig. 6). The same background shading is used to indicate isosteric basepairs in each family.

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Non-Protein Coding RNAs (Springer Series in Biophysics) by Sarah A. Woodson, Robert T. Batey, Nils Walter


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