Thermodynamics and Folding Pathway of Tetraloop Receptor-Mediated RNA Helical Packing

JOURNAL OF MOLECULAR BIOLOGY

卷:384

Article

Meulen, Kirk A. Vander¹  Davis, Jared H.¹  Foster, Trenton R.¹  Record, M. Thomas, Jr.¹  Butcher, Samuel E.¹ 

[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA

关键词: RNA folding;    RNA thermodynamics;    tetraloop receptor;    heat capacity change;    calorimetry;   

DOI  :  10.1016/j.jmb.2008.09.049

来源: Elsevier

【 摘 要 】

Little is known about the thermodynamic forces that drive the folding pathways of higher-order RNA structure. In this study, we employ calorimetric [isothermal titration calorimetry (ITC) and differential scanning calorimetry (DSC)] and spectroscopic (NMR and UV) methods to characterize the thermodynamics of the GAAA tetraloop-receptor interaction, utilizing a previously described bivalent construct. ITC studies indicate that the bivalent interaction is enthalpy driven and highly stable, with a binding constant (K-obs) of 5.5 x 10(6) M-1 and enthalpy (Delta H-obs(o)) of - 33.8 kcal/mol at 45 degrees C in 20 mM KCl and 2 MM MgCl2. Thus, we derive the Delta H-obs(o) for a single tetraloop-receptor interaction to be -16.9 kcal/mol at these conditions. UV absorbance data indicate that an increase in base stacking quality contributes to the enthalpy of complex formation. These highly favorable thermodynamics are consistent with the known critical role for the tetraloop-receptor motif in the folding of large RNAs. Additionally, a significant heat capacity change (Delta C-p,obs(o)) of -0.24 kcal mol(-1) K-1 was determined by ITC. DSC and UV-monitored thermal denaturation experiments indicate that the bivalent tetraloop-receptor construct follows a minimally five-state unfolding pathway and suggest the Delta C-p,obs(o) for the interaction results from a temperature-dependent unbound receptor RNA structure. (C) 2008 Elsevier Ltd. All rights reserved.

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