RCAST, The University of Tokyo, 4-6-1 Komaba, Meguro, Tokyo 153-8904, Japan.
Nanoscale. 2014 Aug 7;6(15):9122-6. doi: 10.1039/c4nr01598c.
A new waffle-like DNA origami assembly (DNA waffle) with nine nanometer-scale wells in a 3 × 3 matrix pattern has been successfully constructed and used as a scaffold for selective nano-patterning of individual protein molecules. The folding pattern of the scaffold was specially designed so that the dimensions of each well could be independently tuned according to the dimensions of the guest nanoparticles. We demonstrated that two distinct proteins, streptavidin (SA) tetramer (d = 5 nm) and anti-fluorescein antibody (IgG) (inter-paratope distance ∼ 14.0 nm), could be selectively captured in size-variable wells of dimensions 6.8 × 12 × 2.0 nm for SA and 6.8 × 12 × 2.0 nm or 10.2 × 12 × 2.0 nm for IgG, respectively, through the attachment of two biotins or two fluoresceins at the two edges of each well. This allowed the formation of a heterogeneous protein nanoarray of individual molecules. The position of SA or IgG capture can be fully controlled by placement of biotins or fluoresceins in the nanoarray well. Moreover, a hetero-nanoarray consisting of two kinds of enzyme: horseradish peroxidase-labeled streptavidin (HRP-SA) and alkaline phosphatase-labeled anti-FITC antibody (AP-IgG) was successfully constructed through selective attachment of biotin or fluorescein in any desired wells. Successful enzyme-heteroarray formation was confirmed by enzymatic activity analyses after purification of mixtures of enzymes and DNA waffles.
一种新型的华夫状 DNA 折纸组装体(DNA 华夫)已成功构建,其在 3×3 矩阵图案中有九个纳米级别的井,可用作单个蛋白质分子的选择性纳米图案化的支架。支架的折叠模式经过专门设计,使得每个井的尺寸可以根据客体纳米颗粒的尺寸独立调节。我们证明了两种不同的蛋白质,链霉亲和素(SA)四聚体(d=5nm)和抗荧光素抗体(IgG)(间隔臂距离约 14.0nm),可以通过在尺寸为 6.8×12×2.0nm 的可变尺寸井中分别附着两个生物素或两个荧光素,选择性地捕获尺寸为 6.8×12×2.0nm 或 10.2×12×2.0nm 的 SA 和 IgG。这允许形成个体分子的异质蛋白质纳米阵列。SA 或 IgG 的捕获位置可以通过在纳米阵列井中放置生物素或荧光素来完全控制。此外,通过在任何所需的井中选择性地附着生物素或荧光素,可以成功构建由两种酶组成的异质纳米阵列:辣根过氧化物酶标记的链霉亲和素(HRP-SA)和碱性磷酸酶标记的抗 FITC 抗体(AP-IgG)。酶-异质阵列的成功形成通过混合物的酶和 DNA 华夫的纯化后的酶活性分析得到证实。