Sorbonne Université , Laboratoire Jean Perrin , F-75005 Paris , France.
UMR 8237, CNRS , F-75005 Paris , France.
Biochemistry. 2019 Jun 11;58(23):2675-2681. doi: 10.1021/acs.biochem.9b00063. Epub 2019 May 29.
In the absence of DNA, a solution containing the four deoxynucleotidetriphosphates (dNTPs), a DNA polymerase, and a nicking enzyme generates a self-replicating mixture of DNA species called parasite. Parasites are problematic in template-based isothermal amplification schemes such as EXPAR as well as in related molecular programming approaches, such as the PEN DNA toolbox. Here we show that using a nicking enzyme with only three letters (C, G, T) in the top strand of its recognition site, such as Nb.BssSI, allows us to change the sequence design of EXPAR templates in a way that prevents the formation of parasites when dATP is removed from the solution. This method allows us to make the EXPAR reaction robust to parasite contamination, a common feature in the laboratory, while keeping it compatible with PEN programs, which we demonstrate by engineering a parasite-proof bistable reaction network.
在没有 DNA 的情况下,含有四种脱氧核苷三磷酸(dNTPs)、DNA 聚合酶和切口酶的溶液会产生一种称为“寄生虫”的自我复制的 DNA 混合物。寄生虫在基于模板的等温扩增方案(如 EXPAR)以及相关的分子编程方法(如 PEN DNA 工具箱)中是一个问题。在这里,我们表明,使用仅在其识别位点的上链中有三个字母(C、G、T)的切口酶,例如 Nb.BssSI,我们可以改变 EXPAR 模板的序列设计,从而在从溶液中去除 dATP 时防止寄生虫的形成。这种方法使 EXPAR 反应能够抵抗寄生虫污染,这是实验室中的一个常见特征,同时又保持与 PEN 程序兼容,我们通过设计一种抗寄生虫的双稳态反应网络来证明这一点。