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Improved thrombin binding aptamer by incorporation of a single unlocked nucleic acid monomer

机译:通过掺入单个未锁定的核酸单体改善凝血酶结合适体

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A 15-mer DNA aptamer (named TBA) adopts a G-quadruplex structure that strongly inhibits fibrin-clot formation by binding to thrombin. We have performed thermodynamic analysis, binding affinity and biological activity studies of TBA variants modified by unlocked nucleic acid (UNA) monomers. UNA-U placed in position U3, U7 or U12 increases the thermodynamic stability of TBA by 0.15-0.50 kcal/mol. In contrast, modification of any position within the two G-quartet structural elements is unfavorable for quadruplex formation. The intramolecular folding of the quadruplexes is confirmed by T-m versus ln c analysis. Moreover, circular dichroism and thermal difference spectra of the modified TBAs displaying high thermodynamic stability show bands that are characteristic for antiparallel quadruplex formation. Surface plasmon resonance studies of the binding of the UNA-modified TBAs to thrombin show that a UNA monomer is allowed in many positions of the aptamer without significantly changing the thrombin-binding properties. The biological effect of a selection of the modified aptamers was tested by a thrombin time assay and showed that most of the UNA-modified TBAs possess anticoagulant properties, and that the construct with a UNA-U monomer in position 7 is a highly potent inhibitor of fibrin-clot formation.
机译:15-mer DNA适体(命名为TBA)采用G-四链体结构,该结构通过与凝血酶结合而强烈抑制纤维蛋白凝集的形成。我们已经对由解锁核酸(UNA)单体修饰的TBA变体进行了热力学分析,结合亲和力和生物学活性研究。将UNA-U放在U3,U7或U12位置可使TBA的热力学稳定性提高0.15-0.50 kcal / mol。相比之下,两个G四重奏结构元素内任何位置的修饰都不利于四链体的形成。通过T-m对lnc分析证实了四链体的分子内折叠。此外,显示出高热力学稳定性的改性TBA的圆二色性和热差光谱显示出具有反平行四链体形成特征的谱带。对UNA修饰的TBA与凝血酶结合的表面等离子体共振研究表明,在适体的许多位置都允许UNA单体,而不会显着改变凝血酶的结合特性。通过凝血酶时间测定法测试了选择的修饰的适体的生物学效应,结果表明,大多数UNA修饰的TBA具有抗凝血特性,并且在位置7处具有UNA-U单体的构建体是强效的Aβ抑制剂。纤维蛋白凝集形成。

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