Ikebukuro Kazunori, Yoshida Wataru, Noma Takahisa, Sode Koji
Department of Life Science and Biotechnology, Tokyo University of Agriculture and Technology, Naka-cho, Koganei, Tokyo, Japan,
Biotechnol Lett. 2006 Dec;28(23):1933-7. doi: 10.1007/s10529-006-9174-8. Epub 2006 Oct 3.
We previously identified a thrombin-inhibiting DNA aptamer that was presumed to form a G-quartet structure with a duplex. To investigate the importance of the sequences in the duplex region and to obtain aptamers with higher inhibitory activities, we randomized the sequences of the duplex region of this aptamer and carried out selection based on inhibitory activity using a genetic algorithm. This method consisted of selection via an inhibition assay, crossover, and mutation in silico. After two cycles, we obtained ligands with greater inhibitory activities than that of the original aptamer. In addition, the duplex sequences were found to contribute to the inhibitory activities of aptamers.
我们之前鉴定出一种凝血酶抑制性DNA适配体,推测其与双链体形成G-四联体结构。为了研究双链体区域序列的重要性并获得具有更高抑制活性的适配体,我们将该适配体双链体区域的序列随机化,并使用遗传算法基于抑制活性进行筛选。该方法包括通过抑制试验进行筛选、交叉和计算机模拟突变。经过两个循环后,我们获得了抑制活性比原始适配体更高的配体。此外,发现双链体序列对适配体的抑制活性有贡献。