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The formation pathway of tetramolecular G-quadruplexes.

机译:四分子G-四链体的形成途径。

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Oligonucleotides containing guanosine stretches associate into tetrameric structures stabilized by monovalent ions. In order to describe the sequence of reactions leading to association of four identical strands, we measured by NMR the formation and dissociation rates of (TGnT)4 quadruplexes (n = 3-6), their dissociation constants and the reaction orders for quadruplex formation. The quadruplex formation rates increase with the salt concentration but weakly depend on the nature (K+, Na+ or Li+) of the counter ions. The activation energies for quadruplex formation are negative. The quadruplex lifetimes strongly increase with the G-tract length and are much more longer in K+ solution than in Na+ or Li+ solutions. The reaction order for quadruplex formation is 3 in 0.125 M KCl and 4 in LiCl solutions. The kinetics measurements suggest that quadruplex formation proceeds step by step via sequential strand association into duplex and triplex intermediate species. Triplex formation is rate limiting in 0.125 MKCl solution. In LiCl, each step of the association process depends on the strand concentration. Parallel reactions to formation of the fully matched canonical quadruplex may result in kinetically trapped mismatched quadruplexes making the canonical quadruplex practically inaccessible in particular at low temperature in KCl solution.
机译:含有鸟苷延伸的寡核苷酸缔合成由一价离子稳定的四聚体结构。为了描述导致四个相同链缔合的反应顺序,我们通过NMR测量了(TGnT)4四链体(n = 3-6)的形成和解离速率,它们的解离常数和四链体形成的反应顺序。四重合物的形成速率随盐浓度的增加而增加,但弱取决于抗衡离子的性质(K +,Na +或Li +)。用于四链体形成的活化能为负。四重金属的寿命随着G轴长度的增加而大大增加,并且在K +溶液中比在Na +或Li +溶液中更长。四联体形成的反应顺序是,在0.125 M KCl中为3,在LiCl溶液中为4。动力学测量结果表明,四链体形成是通过顺序链缔合逐步形成双链体和三链体中间物种而进行的。在0.125 MKCl溶液中三重链的形成限制了速率。在LiCl中,缔合过程的每个步骤都取决于链的浓度。形成完全匹配的典范四联体的平行反应可能会导致动力学捕获的错配四联体,实际上使典范四联体实际上不可访问,尤其是在KCl溶液中的低温下。

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