Vysvětlení sekvenčních preferencí rekurentních RNA motivů pomocí metod kvantové chemie: Dinukleotidová RNA platforma

Mgr. Bc. Arnošt Mládek, Ph.D.

Advanced ('rigorózní') thesis

Understanding the Sequence Preference of Recurrent RNA Building Blocks using Quantum Chemistry: The Itrastrand RNA Dinucleotide Platform

Anotácia:

Cílem předkládané studie je vysvětlení sekvenčních preferencí rekurentních RNA motivů pomocí moderních metod kvantové chemie. Výsledky analýzy potvrzují hypotézu Lu et al. (Xiang-Jun Lu, et al. Nuc. Acids Res. 32 (14), 2010) týkající se mimořádné stability GpU platformy.

Abstract:

Folded RNA molecules are shaped by an astonishing variety of highly conserved non-canonical molecular interactions and backbone topologies. The dinucleotide platform is a widespread recurrent RNA modular building submotif formed by the side-by-side pairing of bases from two consecutive nucleotides within a single strand, with highly specific sequence preferences. This unique arrangement of bases is cemented by an intricate network of noncanonical hydrogen bonds and facilitated by a distinctive backbone topology. The present study investigates the gas-phase intrinsic stabilities of the three most common RNA dinucleotide platforms - 5'-GpU-3', ApA, and UpC - via state-of-the-art quantum-chemical (QM) techniques. The mean stability of base...base interactions decreases with sequence in the order GpU > ApA > UpC. Bader's atoms-in-molecules analysis reveals that the N2(G)...O4(U) hydrogen bond of the GpU platform is stronger than the corresponding H-bonds in the other two platforms. The mixed-pucker sugar-phosphate backbone conformation found in most GpU platforms, in which the 5'-ribose sugar (G) is in the C2'-endo form and the 3'-sugar (U) in the C3'-endo form, is intrinsically more stable than the standard A-RNA backbone arrangement, partially as a result of a favorable O2'...O2P intra-platform interaction. Our results thus validate the hypothesis of Lu et al., (Xiang-Jun Lu, et al. Nuc. Acids Res. 32 (14), 2010), that the superior stability of GpU platforms is partially mediated by the strong O2'...O2P hydrogen bond. In contrast, ApA and especially UpC platform-compatible backbone conformations are rather diverse and do not display any characteristic structural features. The average stabilities of ApA and UpC derived backbone conformers are also lower than those of GpU platforms. Thus, the observed structural and evolutionary patterns of the dinucleotide platforms can be accounted for, to a large extent, by their intrinsic properties as described by modern QM calculations. Our analysis of published and new molecular dynamics simulation data, however, shows that the dinucleotide platform is not properly described in the course of atomistic explicit-solvent simulations. Our work also gives methodological insights into QM calculations of experimental RNA backbone geometries. Such calculations are inherently complicated by rather large data and refinement uncertainties in the available RNA experimental structures, which often preclude reliable energy computations.

Keywords

RNA structure, QM calculations, Dinucleotide platforms, GpU, ApA, UpC, RNA backbone, RNA submotif, O2'...O2P Interakce

Jazyk práce: English

Datum vytvoření / odevzdání či podání práce: 4. 10. 2011

Obhajoba závěrečné práce

• Obhajoba proběhla 21. 12. 2011
• Oponent: Mgr. Daniel Svozil, Ph.D., Mgr. Kamila Réblová, Ph.D.

Masaryk University

Faculty of Science

Advanced ('rigorózní řízení') programme / odbor:
Physics / Biophysics