Asanuma Hiroyuki, Matsunaga Daijiro, Komiyama Makoto
Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Chikusa, Nagoya 464-8603, Japan.
Nucleic Acids Symp Ser (Oxf). 2005(49):35-6. doi: 10.1093/nass/49.1.35.
Multiple azobenzenes were introduced into the oligonucleotide on D-threoninol for the clear-cut photo-regulation of the formation and dissociation of DNA duplex. When azobenzenes took trans form, introduction of multiple azobenzenes (azobenzenes:nucleobases = 1:2) did not interfere with duplex formation at all compared with their native duplex. In contrast, melting temperature (Tm) uniformly decreased with the number of azobenzenes when they took cis-form. As a result, clear-cut photo-regulation of the duplex formation was attained under physiological conditions. Furthermore, nearest-neighbor parameters for these azobenzene-tethered oligonucleotides were obtained. It was found that Tms estimated from these parameters well coincided with those of measured ones.
将多个偶氮苯引入到基于D-苏糖醇的寡核苷酸中,以实现对DNA双链体形成和解离的清晰光调控。当偶氮苯呈反式构型时,与天然双链体相比,引入多个偶氮苯(偶氮苯:核苷酸碱基 = 1:2)根本不会干扰双链体的形成。相反,当偶氮苯呈顺式构型时,解链温度(Tm)会随着偶氮苯数量的增加而均匀降低。结果,在生理条件下实现了对双链体形成的清晰光调控。此外,还获得了这些偶氮苯连接的寡核苷酸的近邻参数。发现根据这些参数估算的Tm值与测量值非常吻合。