Thermodynamic characterization of an engineered tetracycline-binding riboswitch

• Published in: Nucleic acids research 2006-01, Vol.34 (9), p.2607-2617
• Main Authors: Müller, Michael, Weigand, Julia E., Weichenrieder, Oliver, Suess, Beatrix
• Format: Article
• Language: English
• Subjects: Aptamers, Nucleotide - chemistry; Base Sequence; Binding Sites; Calorimetry; Entropy; Gene Expression Regulation; Genetic Engineering; Molecular Sequence Data; Nucleic Acid Conformation; Protein Biosynthesis; Ribosomes - metabolism; RNA - chemistry; Tetracycline - chemistry; Thermodynamics
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkl347

Riboswitches reflect a novel concept in gene regulation that is particularly suited for technological adaptation. Therefore, we characterized thermodynamically the ligand binding properties of a synthetic, tetracycline (tc)-binding RNA aptamer, which regulates gene expression in a dose-dependent manner when inserted into the untranslated region of an mRNA. In vitro, one molecule of tc is bound by one molecule of partially pre-structured and conformationally homogeneous apo-RNA. The dissociation constant of 770 pM, as determined by fluorimetry, is the lowest reported so far for a small molecule-binding RNA aptamer. Additional calorimetric analysis of RNA point mutants and tc derivatives identifies functional groups crucial for the interaction and including their respective enthalpic and entropic contributions we can propose detailed structural and functional roles for certain groups. The conclusions are consistent with mutational analyses in vivo and support the hypothesis that tc-binding reinforces the structure of the RNA aptamer, preventing the scanning ribosome from melting it efficiently.