Laboratory of Gene Biodynamics, Graduate School of Biostudies, Kyoto University, Oiwake-cho, Kitashirakawa, Sakyo-ku, Kyoto 606-8502, Japan.
Nat Nanotechnol. 2011 Feb;6(2):116-20. doi: 10.1038/nnano.2010.268. Epub 2011 Jan 16.
Synthetic nanostructures consisting of biomacromolecules such as nucleic acids have been constructed using bottom-up approaches. In particular, Watson-Crick base pairing has been used to construct a variety of two- and three-dimensional DNA nanostructures. Here, we show that RNA and the ribosomal protein L7Ae can form a nanostructure shaped like an equilateral triangle that consists of three proteins bound to an RNA scaffold. The construction of the complex relies on the proteins binding to kink-turn (K-turn) motifs in the RNA, which allows the RNA to bend by ∼ 60° at three positions to form a triangle. Functional RNA-protein complexes constructed with this approach could have applications in nanomedicine and synthetic biology.
采用自下而上的方法构建了由生物大分子(如核酸)组成的合成纳米结构。特别是,利用沃森-克里克碱基配对构建了各种二维和三维 DNA 纳米结构。在这里,我们表明 RNA 和核糖体蛋白 L7Ae 可以形成一种等边三角形形状的纳米结构,该结构由三个与 RNA 支架结合的蛋白质组成。该复合物的构建依赖于蛋白质与 RNA 中的扭结-转角(K-turn)基序结合,这允许 RNA 在三个位置弯曲约 60°形成三角形。使用这种方法构建的功能性 RNA-蛋白质复合物在纳米医学和合成生物学中有应用前景。