Petree Jessica R, Yehl Kevin, Galior Kornelia, Glazier Roxanne, Deal Brendan, Salaita Khalid
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University , Atlanta, Georgia 30322, United States.
ACS Chem Biol. 2018 Jan 19;13(1):215-224. doi: 10.1021/acschembio.7b00437. Epub 2017 Dec 19.
Modifying RNA through either splicing or editing is a fundamental biological process for creating protein diversity from the same genetic code. Developing novel chemical biology tools for RNA editing has potential to transiently edit genes and to provide a better understanding of RNA biochemistry. Current techniques used to modify RNA include the use of ribozymes, adenosine deaminase, and tRNA endonucleases. Herein, we report a nanozyme that is capable of splicing virtually any RNA stem-loop. This nanozyme is comprised of a gold nanoparticle functionalized with three enzymes: two catalytic DNA strands with ribonuclease function and an RNA ligase. The nanozyme cleaves and then ligates RNA targets, performing a splicing reaction that is akin to the function of the spliceosome. Our results show that the three-enzyme reaction can remove a 19 nt segment from a 67 nt RNA loop with up to 66% efficiency. The complete nanozyme can perform the same splice reaction at 10% efficiency. These splicing nanozymes represent a new promising approach for gene manipulation that has potential for applications in living cells.
通过剪接或编辑来修饰RNA是一个基本的生物学过程,可从相同的遗传密码中创造蛋白质多样性。开发用于RNA编辑的新型化学生物学工具具有瞬时编辑基因并更好地理解RNA生物化学的潜力。目前用于修饰RNA的技术包括使用核酶、腺苷脱氨酶和tRNA内切核酸酶。在此,我们报道了一种几乎能够剪接任何RNA茎环的纳米酶。这种纳米酶由一个用三种酶功能化的金纳米颗粒组成:两条具有核糖核酸酶功能的催化DNA链和一种RNA连接酶。该纳米酶切割然后连接RNA靶标,进行类似于剪接体功能的剪接反应。我们的结果表明,三酶反应可以从67 nt的RNA环中去除19 nt的片段,效率高达66%。完整的纳米酶可以以10%的效率进行相同的剪接反应。这些剪接纳米酶代表了一种新的有前途的基因操作方法,具有在活细胞中应用的潜力。