University of Bordeaux, CNRS UMR 5320, INSERM U1212, Bordeaux 33076, France.
Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
Nucleic Acids Res. 2018 Feb 16;46(3):1052-1058. doi: 10.1093/nar/gkx1267.
Nucleic acids are biomolecules of amazing versatility. Beyond their function for information storage they can be used for building nano-objects. We took advantage of loop-loop or kissing interactions between hairpin building blocks displaying complementary loops for driving the assembly of nucleic acid nano-architectures. It is of interest to make the interaction between elementary units dependent on an external trigger, thus allowing the control of the scaffold formation. To this end we exploited the binding properties of structure-switching aptamers (aptaswitch). Aptaswitches are stem-loop structured oligonucleotides that engage a kissing complex with an RNA hairpin in response to ligand-induced aptaswitch folding. We demonstrated the potential of this approach by conditionally assembling oligonucleotide nanorods in response to the addition of adenosine.
核酸是具有惊人多功能性的生物分子。除了用于信息存储的功能外,它们还可以用于构建纳米物体。我们利用发夹构建块之间的环-环或亲吻相互作用,这些构建块显示互补的环,用于驱动核酸纳米结构的组装。使基本单元之间的相互作用依赖于外部触发因素,从而可以控制支架形成,这是很有趣的。为此,我们利用结构转换适体(aptaswitch)的结合特性。适体开关是茎环结构的寡核苷酸,当配体诱导适体开关折叠时,与 RNA 发夹形成亲吻复合物。我们通过在添加腺苷时条件组装寡核苷酸纳米棒证明了这种方法的潜力。