Tajima Kaori, Kim Won-Jong, Akaike Toshihiro, Maruyama Atsushi
Department of Biomolecular Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori, Yokohama 226-8501, Japan.
Nucleic Acids Res Suppl. 2002(2):265-6. doi: 10.1093/nass/2.1.265.
In previous reports, we have demonstrated that the cationic comb-type copolymers (PLL-g-Dex) having a poly-L-lysine main chain and dextran side chains stabilized DNA duplex and triplex. Furthermore, the copolymer was found to accelerate more than 20,000 folds strand exchange reaction between 20 bp duplex and its homologous single strand (1). This study was designed to inspect structural factor of polycationic moieties in acceleration effects. To this end, polypeptides containing lysine or arginine moieties as cationic groups were examined in their potency to accelerating strand exchange reaction. It was shown that arginine-rich peptide showed higher accelerating effect than lysine peptide when total positive charges of peptides were kept constant.
在之前的报告中,我们已经证明,具有聚-L-赖氨酸主链和葡聚糖侧链的阳离子梳型共聚物(PLL-g-Dex)可稳定DNA双链体和三链体。此外,还发现该共聚物能使20bp双链体与其同源单链之间的链交换反应加速超过20000倍(1)。本研究旨在考察聚阳离子部分在加速效应中的结构因素。为此,对含有赖氨酸或精氨酸部分作为阳离子基团的多肽加速链交换反应的能力进行了研究。结果表明,当多肽的总正电荷保持恒定时,富含精氨酸的肽比赖氨酸肽具有更高的加速效果。