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Kinetic resolution of bimolecular hybridization versus intramolecular folding in nucleic acids by surface plasmon resonance: application to G-quadruplex/duplex competition in human c-myc promoter

机译:通过表面等离子体共振在核酸中双分子杂交与分子内折叠的动力学拆分:在人类c-myc启动子的G-四链体/双链体竞争中的应用

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The human oncogene c-myc is regulated by G-quadruplex formation within the nuclease hypersensitive element (NHE IIII) in the c-myc promoter, making the quadruplex a strong anti-cancer target. With respect to this, the competing equilibrium between intramolecular quadruplex folding and bimolecular duplex formation is poorly understood and very few techniques have addressed this problem. We present a method for simultaneously determining the kinetic constants for G-quadruplex folding/unfolding and hybridization in the presence of the complementary strand from a single reaction using an optical biosensor based on surface plasmon resonance (SPR). Using this technique, we demonstrate for the first time that quadruplex formation in the c-myc promoter is favored at low strand concentrations. Our results indicate favorable quadruplex folding (equilibrium folding constant KF of 2.09 calculated from the kinetic parameters: folding rate constant, kf = 1.65 × 10?2 s?1 and unfolding rate constant, ku = 7.90 × 10?3 s?1) in 150 mM K+. The hybridization rate constants detected concurrently gave a bimolecular association constant, ka = 1.37 × 105 M?1 s?1 and dissociation constant, kd = 4.94 × 10?5 s?1. Interestingly, in the presence of Na+ we observed that G-quadruplex folding was unfavorable (KF = 0.54). Implication of our results on the c-myc transcription activation model is discussed in light of aberrant c-myc expression observed on destabilization of the G-quadruplex.
机译:人类致癌基因c-myc由c-myc启动子中的核酸酶超敏元件(NHE III I )中的G-四链体形成调控,从而使四链体成为强大的抗癌靶标。对此,人们对分子内四链体折叠和双分子双链体形成之间的竞争平衡了解得很少,并且很少有技术解决这个问题。我们提出了一种方法,该方法同时使用基于表面等离振子共振(SPR)的光学生物传感器,从单个反应中,在互补链存在的情况下,同时确定G-四链体折叠/解折叠和杂交的动力学常数。使用这种技术,我们首次证明了c-myc启动子中的四链体形成在低链浓度下是有利的。我们的结果表明,有利的四链折叠(平衡折叠常数K F 由动力学参数:折叠速率常数k f = 1.65×10 ?2 < / sup> s ?1 和展开速率常数k u = 7.90×10 ?3 s ?1 )在150 mM K + 中。同时检测到的杂交速率常数为双分子缔合常数,k a = 1.37×10 5 M ?1 s ?1 < / sup>和解离常数k d = 4.94×10 ?5 s ?1 。有趣的是,在Na + 存在的情况下,我们观察到G-四链体折叠是不利的(K F = 0.54)。鉴于在G-四链体失稳时观察到的异常c-myc表达,讨论了我们的结果对c-myc转录激活模型的影响。

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