Large noncoding RNAs fold into their biologically functional structures via compact yet disordered intermediates, which couple the stable secondary structure of the RNA with the emerging tertiary fold. The specificity of the collapse transition, which coincides with the assembly of helical domains, depends on RNA sequence and counterions. It determines the specificity of the folding pathways and the magnitude of the free energy barriers to the ensuing search for the native conformation. By coupling helix assembly with nascent tertiary interactions, compact folding intermediates in RNA also play a crucial role in ligand binding and RNA-protein recognition.
机构:
Washington Univ, Mol Biophys Program, St Louis, MO 63130 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Chen, Alan A.
;
Draper, David E.
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Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Draper, David E.
;
Pappu, Rohit V.
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Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Washington Univ, Ctr Computat Biol, St Louis, MO 63130 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
机构:
Washington Univ, Mol Biophys Program, St Louis, MO 63130 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Chen, Alan A.
;
Draper, David E.
论文数: 0引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Draper, David E.
;
Pappu, Rohit V.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
Washington Univ, Ctr Computat Biol, St Louis, MO 63130 USAWashington Univ, Dept Biomed Engn, St Louis, MO 63130 USA