Kuzuya Akinori, Numajiri Kentaro, Kimura Mayumi, Komiyama Makoto
RCAST, The University of Tokyo, Meguro, Tokyo 153-8904, Japan.
Nucleic Acids Symp Ser (Oxf). 2008(52):681-2. doi: 10.1093/nass/nrn344.
Tape-like DNA nanostructures of 26 nm width with regularly arranged nanometer-scale wells have been prepared by bundling nine DNA helices. Just one streptavidin tetramer (d = 5 nm) is size-selectively captured in each 6.8 x 10 x 2.0 nm well when two biotins are attached to two opposite edges of the well. Accordingly, precise streptavidin nanoarray of 28 nm periods is constructed. The tetramers captured in the wells showed remarkable stability under repetitive AFM scanning. On the other hand, double-sized wells accommodated two tetramers inside, presumably because the distance between the two biotins is too large to cooperatively "anchor" a tetramer.
通过将九条DNA螺旋束在一起,制备出了宽度为26纳米、带有规则排列的纳米级孔的带状DNA纳米结构。当在每个6.8×10×2.0纳米的孔的两个相对边缘连接两个生物素时,每个孔中尺寸选择性地捕获一个链霉亲和素四聚体(直径 = 5纳米)。据此,构建了周期为28纳米的精确链霉亲和素纳米阵列。在重复的原子力显微镜扫描下,捕获在孔中的四聚体显示出显著的稳定性。另一方面,双倍尺寸的孔内部容纳了两个四聚体,推测是因为两个生物素之间的距离太大,无法协同“锚定”一个四聚体。