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This work investigates pathways of conformational transitions in ubiquitous RNA structural motifs. In our lab, we have developed multi-scale structural datamining techniques for identification of three-dimensional structural patterns in high-resolution crystal structures of globular RNA. I have applied these techniques to identify variations in the conformations of RNA double-helices and tetraloops. The datamined structural information is used to propose reaction coordinates for conformational transitions involved in double-strand helix propagation and tetraloop folding in RNA. I have also presented an algorithm to identify stacked RNA bases. In this work, experimentally derived thermodynamic evaluation of the conformations has been used to as an additional parameter to add detail to RNA structural transitions. RNA conformational transitions help control processes in small systems such as riboswitches and in large systems such as ribosomes. Adopting functional conformations by globular RNA during a folding process also involves structural transitions. RNA double-helices and tetraloops are common, ubiquitous structural motifs in globular RNA that independently fold in to a thermodynamically stable conformation. Folding models for these motifs are proposed in this work with probable intermediates ordered along the reaction coordinates. We hypothesize that frequently observed structural states in crystals structures are analogous in conformation to stable thermodynamic â on-pathwayâ folded states. Conversely, we hypothesize that conformations that are rarely observed are improbable folding intermediates, i.e., these conformational states are â off-pathwayâ states. In general on-pathway states are assumed to be thermodynamically more stable than off-pathway states, with the exception of kinetic traps. Structural datamining shows that double helices in RNA may propagate by the â stack-ratchetâ mechanism proposed here instead of the commonly accepted zipper mechanism. Mechanistic models for RNA tetraloop folding have been proposed and validated with experimentally derived thermodynamic data. The extent of stacking between bases in RNA is variable, indicating that stacking may not be a two-state phenomenon. A novel algorithm to define and identify stacked bases at atomic resolution has also been presented in this work.

RNA is amazing. We found that without changing the backbone connectivity, RNA can maintain structural conservation in 3D via topology switches, at a single residue level. I developed a method of representing RNA structure in multiresolution, called the PBR approach (P stands for Phosphate; B stands for Base; R stands for Ribose). In this method, structural data is viewed through a series of resolutions from finest to coarsest. At a single nucleotide resolution (fine resolution), RNA is abstruse and elaborate with structural insertions/deletions, strand clips, and 3,2-switches. The compilation of structural deviations of RNA, called DevLS (Deviations of Local Structure), provides a new descriptive language of RNA structure, allowing one to systematize and investigate RNA structure. Using PBR analysis, a total of 103 tetraloops within the crystal structures of the 23s rRNA of H. marismortui and the 70s rRNA of T. thermophilus are found and classified. Combining them, I constructed a 'tetraloop family tree', using a tree formalism, to unify and re-define the tetraloop motif and to represent relationships between tetraloops, as grouped by DevLS. To date, structural alignment of very large RNAs remains challenge due to the large size, intricate backbone choreography, and tertiary interactions. To overcome these obstacles, I developed a concept of structural anchors along with a 'Divide and Conquer' strategy for performing superimposition of 23s rRNAs. The successful alignment and superimpositions of the 23s rRNAs of T. thermophilus and H. marismortui gives an overall RMSD of atomic positions of 1.2 Å, as utilized 73% of RNA backbone atoms (~ 2129 residues). By using principles of inorganic chemistry along with structural alignment technique as described above, a recurrent magnesium-binding motif in large RNAs is revealed. These magnesium-binding motifs play a critical role in the framework of the ribosomal PTC by their locations, topologies, and coordination geometries. Common features of Mg2+-mc's include direct phosphate chelation of two magnesium ions in the form of Mg2+(i)-(O1P-P-O2P)-Mg2+(j), phosphate groups of adjacent RNA residues as ligands of a given Mg2+, and undulated RNA surfaces with unpaired and unstacked bases.

RNA tetraloop is the smallest, simplest and the most frequent motif which is involved in numerous important biological functions. A local deviation from the RNA standard tetraloop, d2 tetraloop, has been identified with high abundance in 5S, 16S and 23S rRNAs. The presence of d2 tetraloops in highly conserved regions of 16S and 23S rRNAs suggests their functional importance. With one less residue in the loop, d2 tetraloops are considered more energetically restrained and less stable than standard tetraloops. The deletion at position j+2 in the loop is always correlated with adjacent stem distortion. MD simulations of 314-d2-tetraloop (a sample structure of d2 tetraloops) and cutd2-tetraloop (an artificially built perfect d2 tetraloop with no stem defects) have shown that stem defects are the stabilizing factor of d2 tetraloops. Simulations have also revealed that the insertion residue 318C (an example of stem defect) is stabilizing 314-d2-tetraloop by forming hydrogen bonding interactions with both the loop and the stem. When these two hydrogen bonding interactions are eliminated, the structure remained relatively stable compared to cutd2-tetraloop where the insertion residue was completely removed from the stem. This suggests the insertion residue is also stabilizing 314-d2-tetraloop by providing some conformational relaxation in the stem. Investigation of RNA standard tetraloop high temperature unfolding has revealed that the d2 tetraloop is possibly a kinetically trapped intermediate state during the folding of the standard tetraloop. High temperature unfolding simulations of standard tetraloop have shown a three-state folding behavior: a folded state, an intermediate state and an unfolded state. The folding of standard tetraloop starts with the formation of the loop. The closing base pair forms first, followed by the loop and the stem which form critical interactions such as base pairing and stacking that make a tetraloop. ROMP PNB has been investigated as supports to immobilize homogeneous catalysts to achieve both high reactivity and selectivity and easy separation. Polymers with intermediate conformational order can increase the accessibility of tethered homogeneous catalysts. Simulations of ROMP PNBDC_UD have shown the importance of bulky side groups in enabling the polymer to adopt a helical conformation. Such helical conformations have been associated with intermediate structural order in similar polymers such as PNB made by non-ROMP mechanisms. This intermediate order manifests itself as a split in the amorphous halo of WAXD pattern. Bulk simulations generated WAXD patterns that are close to the experimentally generated WAXD patterns where there are two split peaks: lower angle peak representing intermolecular interaction and higher angle peak representing intramolecular interaction.