Barbeyron Renaud, Vasseur Jean-Jacques, Smietana Michael
Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS-Université Montpellier 1 et Université Montpellier 2 , Place Bataillon , 34095 Montpellier , France . Email:
Chem Sci. 2015 Jan 1;6(1):542-547. doi: 10.1039/c4sc03028a. Epub 2014 Oct 28.
In the area of artificial genetics the development of non-enzymatic self-organization of synthetic building blocks is critical for both providing biopolymers with extended functions and understanding prebiotic processes. While reversibility is believed to have played a major role in early functional genetic materials, we previously reported an efficient DNA-templated ligation of suitably designed 5'-end boronic acid and 3'-end ribonucleosidic half-sequences. Here, we report the enzyme-free and activation-free DNA- and RNA-templated assembly of bifunctional hexamers. The reversible assembly was found to be regio- and sequence specific and the stabilities of the resulting duplexes were compared to their nicked counterparts. To go further with our understanding of this unprecedented process we also examined an auto-templated duplex self-assembly representing a key step toward the evolution of sequence-defined synthetic polymers.
在人工遗传学领域,合成构件的非酶促自组装发展对于赋予生物聚合物扩展功能以及理解益生元过程都至关重要。虽然可逆性被认为在早期功能性遗传物质中发挥了主要作用,但我们之前报道了一种经过适当设计的5'-端硼酸和3'-端核糖核苷半序列的高效DNA模板连接。在此,我们报告了双功能六聚体的无酶且无活化的DNA和RNA模板组装。发现这种可逆组装具有区域和序列特异性,并将所得双链体的稳定性与其带切口的对应物进行了比较。为了进一步理解这一前所未有的过程,我们还研究了一种自模板双链体自组装,它代表了序列定义的合成聚合物进化的关键一步。