Yoshitomi Toru, Wayama Fumiya, Kimura Keiko, Wakui Koji, Furusho Hitoshi, Yoshimoto Keitaro
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo.
Chemical General Division, Nissan Chemical Industries, Ltd.
Anal Sci. 2019;35(1):113-116. doi: 10.2116/analsci.18SDN05.
Here, we demonstrated a strategy for developing signaling aptamers, based on screening of signaling aptamers from multiple aptamer candidates obtained by SELEX with next generation sequencing. Among aptamer candidates labelled by 6-carboxyfluorescein and quencher at both end termini, there is the possibility of discovering a potent signaling aptamer. In this study, we discovered DNA signaling aptamers against VEGFR-1. This strategy has the potential for signaling aptamer discovery without the extremely laborious task of optimization of oligodeoxynucleotide modifications.
在此,我们展示了一种开发信号适体的策略,该策略基于通过下一代测序从通过指数富集的配体系统进化(SELEX)获得的多个适体候选物中筛选信号适体。在两端均用6-羧基荧光素和猝灭剂标记的适体候选物中,有可能发现一种有效的信号适体。在本研究中,我们发现了针对血管内皮生长因子受体-1(VEGFR-1)的DNA信号适体。该策略具有发现信号适体的潜力,而无需进行优化寡脱氧核苷酸修饰这一极其费力的任务。