Univ. Bordeaux, Laboratoire ARNA, F-33000 Bordeaux, France.
Biochimie. 2012 Sep;94(9):1891-9. doi: 10.1016/j.biochi.2012.04.025. Epub 2012 May 10.
Complexes involving three DNA strands were used to demonstrate that the single-cycle kinetics (SCK) method, which consists in injecting sequentially samples at increasing concentrations and until now used exclusively to investigate bimolecular complexes by surface plasmon resonance, can be extended to the kinetic analysis of ternary complexes. DNA targets, B, were designed with sequences of variable lengths on their 3' sides that recognise a surface-immobilized biotinylated DNA anchor, A. These targets displayed on their 5' sides sequences that recognise DNA oligonucleotides of variable lengths, C, namely the analytes. Combinations of B and C DNA oligonucleotides on A generated ternary complexes each composed of two Watson-Crick helices displaying different kinetic properties. The target-analyte B-C duplexes were formed by sequentially injecting three increasing concentrations of the analytes C during the dissociation phase of the target B from the anchor A. The sensorgrams for the target-analyte complexes dissociating from the functionalized surface were successfully fitted by the SCK method while the target dissociated from the anchor, i.e. on a decaying surface. Within the range of applicability of the method which is driven by the rate of dissociation of the target from the anchor, the rate and equilibrium constants characteristic of these target-analyte duplexes of the ternary complexes did not depend on how fast the targets dissociated from the immobilized DNA anchor. In addition the results agreed very well with those obtained when such duplexes were analysed directly as bimolecular complexes, i.e. when the target, modified with a biotin, was directly immobilized onto a streptavidin sensor chip surface rather than captured by an anchor. Therefore the method we named SCKODS (Single-Cycle Kinetics On a Decaying Surface) can also be used to investigate complexes formed during a dissociation phase, in a ternary complex context. The SCKODS method can be combined with the SCK one to fully characterize the two bimolecular complexes of a ternary complex.
使用涉及三股 DNA 链的复合物证明了单循环动力学 (SCK) 方法,该方法包括依次注入浓度递增的样品,直到现在,该方法仅用于通过表面等离子体共振研究双分子复合物,可以扩展到三元复合物的动力学分析。设计 DNA 靶标 B,其 3' 端的序列长度可变,可识别固定在表面的生物素化 DNA 锚定物 A。这些靶标在其 5' 端的序列识别长度可变的 DNA 寡核苷酸 C,即分析物。A 上的 B 和 C DNA 寡核苷酸的组合生成了每个由两个显示不同动力学特性的 Watson-Crick 螺旋组成的三元复合物。通过在靶标 B 从锚定物 A 解吸阶段,依次注入三种递增浓度的分析物 C,形成靶标-分析物 B-C 双链体。从功能化表面解离的靶标-分析物复合物的传感器图可以通过 SCK 方法成功拟合,而目标从锚定物解离,即从衰减表面解离。在该方法的适用范围内,该方法由目标从锚定物解离的速率驱动,这些三元复合物的靶标-分析物双链体的特征速率和平衡常数与目标从固定化 DNA 锚定物解离的速度无关。此外,结果与直接作为双分子复合物分析这些双链体时获得的结果非常吻合,即当用生物素修饰的靶标直接固定在链霉亲和素传感器芯片表面而不是被锚定物捕获时。因此,我们命名为 SCKODS(衰减表面上的单循环动力学)的方法也可用于研究三元复合物的解离相期间形成的复合物。SCKODS 方法可以与 SCK 方法结合使用,以完全表征三元复合物的两个双分子复合物。