Department of Chemistry, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc. 2017 Feb 15;139(6):2464-2467. doi: 10.1021/jacs.6b12731. Epub 2017 Feb 7.
We have developed an unnatural base pair (UBP) and a semisynthetic organism (SSO) that imports the constituent unnatural nucleoside triphosphates and uses them to replicate DNA containing the UBP. However, propagation of the UBP is at least in part limited by the stability of the unnatural triphosphates, which are degraded by cellular and secreted phosphatases. To circumvent this problem, we now report the synthesis and evaluation of unnatural triphosphates with their β,γ-bridging oxygen replaced with a difluoromethylene moiety, yielding dNaMTP and dTPT3TP. We find that although dNaMTP cannot support in vivo replication, likely due to poor polymerase recognition, dTPT3TP can, and moreover, its increased stability can contribute to increased UBP retention. The data demonstrate the promise of this chemical approach to SSO optimization, and suggest that other modifications should be sought that confer phosphatase resistance without interfering with polymerase recognition.
我们开发了一种非天然碱基对(UBP)和一种半合成生物体(SSO),该生物体可导入组成非天然核苷三磷酸,并利用它们复制含有 UBP 的 DNA。然而,UBP 的繁殖至少部分受到非天然三磷酸酯稳定性的限制,这些三磷酸酯被细胞和分泌的磷酸酶降解。为了解决这个问题,我们现在报告了具有β,γ-桥接氧被二氟亚甲基取代的非天然三磷酸酯的合成和评价,得到了 dNaMTP 和 dTPT3TP。我们发现,尽管 dNaMTP 不能支持体内复制,可能是由于聚合酶识别能力差,但 dTPT3TP 可以,而且它的稳定性增加有助于增加 UBP 的保留。这些数据表明了这种化学方法优化 SSO 的前景,并表明应该寻求其他修饰方法,这些修饰方法应具有抗磷酸酶的作用,而不干扰聚合酶的识别。