Energetics of a strongly pH dependent RNA tertiary structure in a frameshifting pseudoknot

被引:71
作者
Nixon, PL [1 ]
Giedroc, DP [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, Ctr Macromol Design, College Stn, TX 77843 USA
关键词
RNA; thermodynamics; pseudoknot; frameshifting; energetics;
D O I
10.1006/jmbi.1999.3464
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Retroviruses employ -1 translational frameshifting to regulate the relative concentrations of structural and non-structural proteins critical to the viral life cycle. The 1.6 Angstrom crystal structure of the -1 frameshifting pseudoknot from beet western yellows virus reveals, in addition to Watson-Crick base-pairing, many loop-stem RNA tertiary structural interactions and a bound Na+. Investigation of the thermodynamics of unfolding of the beet western yellows virus pseudoknot reveals strongly pH-dependent loop-stem tertiary structural interactions which stabilize the molecule, contributing a net of Delta H approximate to - 30 kcal mol(-1) and Delta G(37)degrees, of -3.3 kcal mol(-1) to a total Delta H and aG(37)degrees, of -121 and -16 kcal mol(-1), respectively, at pH 6.0, 0.5 M K+ by DSC. Characterization of mutant RNAs supports the presence of a C8(+).G12-C26 loop 1-stem 2 base-triple (pK(a) = 6.8), protonation of which contributes nearly -3.5 kcal mol(-1.) in net stability in the presence of a wild-type loop 2. Substitution of the nucleotides in loop 2 with uridine bases, which would eliminate the minor groove triplex, destroys pseudoknot formation. An examination of the dependence of the monovalent ion and type on melting profiles suggests that tertiary structure unfolding occurs in a manner quantitatively consistent with previous studies on the stabilizing effects of K+, NH4+ and Na+ on other simple duplex and pseudoknotted RNAs. (C) 2000 Academic Press.
引用
收藏
页码:659 / 671
页数:13
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