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      Coaxial stacking of helixes enhances binding of oligoribonucleotides and improves predictions of RNA folding.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Base Sequence, Calorimetry, Introns, Molecular Sequence Data, Nucleic Acid Conformation, Oligoribonucleotides, chemistry, Phylogeny, RNA, genetics, RNA, Bacterial, RNA, Fungal, Rats, Structure-Activity Relationship

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          Abstract

          An RNA model system consisting of an oligomer binding to a 4-nt overhang at the 5' end of a hairpin stem provides thermodynamic parameters for helix-helix interfaces. In a sequence-dependent manner, oligomers bind up to 1000-fold more tightly adjacent to the hairpin stem than predicted for binding to a free tetramer at 37 degrees C. For the interface (/) in [formula: see text] additional free energy change, delta delta G 37 degrees, for binding is roughly the nearest-neighbor delta G 37 degrees for propagation of an uninterrupted helix of equivalent sequence, CGGC. When X and Z are omitted, the delta delta 37 degrees is even more favorable by approximately 1 kcal/mol (1 cal = 4.184J). On average, predictions of 11 RNA secondary structures improve from 67 to 74% accuracy by inclusion of similar stacking contributions.

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