Schultze P, Macaya R F, Feigon J
Department of Chemistry and Biochemistry, University of California, Los Angeles 90024.
J Mol Biol. 1994 Feb 4;235(5):1532-47. doi: 10.1006/jmbi.1994.1105.
The DNA oligonucleotide d(GGTTGGTGTGGTTGG) (thrombin aptamer) binds to thrombin and inhibits its enzymatic activity in the chain of reactions that lead to blood clotting. Two-dimensional 1H NMR studies indicate that the oligonucleotide forms a folded structure in solution, composed of two guanine quartets connected by two T-T loops spanning the narrow grooves at one end and a T-G-T loop spanning a wide groove at the other end. We present the assignment strategy used, methods for the structure determination, and the refined three-dimensional structure of the thrombin aptamer. The initial structures were generated by metric matrix distance geometry using distance and dihedral bond angle constraints from NOE and coupling constants, respectively, and refined by restrained molecular dynamics and direct NOE refinement. Knowledge of the three-dimensional structure of this thrombin aptamer may be relevant for the design of improved thrombin-inhibiting anti-coagulants with similar structural motifs.
DNA 寡核苷酸 d(GGTTGGTGTGGTTGG)(凝血酶适体)与凝血酶结合,并在导致血液凝固的反应链中抑制其酶活性。二维 1H NMR 研究表明,该寡核苷酸在溶液中形成一种折叠结构,由两个鸟嘌呤四重体组成,两个鸟嘌呤四重体通过两个跨越一端窄沟的 T-T 环相连,另一端有一个跨越宽沟的 T-G-T 环。我们展示了所使用的归属策略、结构测定方法以及凝血酶适体的精制三维结构。初始结构通过度量矩阵距离几何法生成,分别使用来自 NOE 和耦合常数的距离和二面角键角约束,并通过受限分子动力学和直接 NOE 精制进行优化。了解这种凝血酶适体的三维结构可能与设计具有相似结构基序的改进型凝血酶抑制抗凝剂有关。