Lacroix-Labonté Julie, Girard Nicolas, Dagenais Pierre, Legault Pascale
Département de Biochimie et Médecine Moléculaire, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Montréal, QC H3C 3J7, Canada.
Département de Biochimie et Médecine Moléculaire, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Montréal, QC H3C 3J7, Canada
Nucleic Acids Res. 2016 Aug 19;44(14):6924-34. doi: 10.1093/nar/gkw401. Epub 2016 May 10.
The Neurospora VS ribozyme is a catalytic RNA that has the unique ability to specifically recognize and cleave a stem-loop substrate through formation of a highly stable kissing-loop interaction (KLI). In order to explore the engineering potential of the VS ribozyme to cleave alternate substrates, we substituted the wild-type KLI by other known KLIs using an innovative engineering method that combines rational and combinatorial approaches. A bioinformatic search of the protein data bank was initially performed to identify KLIs that are structurally similar to the one found in the VS ribozyme. Next, substrate/ribozyme (S/R) pairs that incorporate these alternative KLIs were kinetically and structurally characterized. Interestingly, several of the resulting S/R pairs allowed substrate cleavage with substantial catalytic efficiency, although with reduced activity compared to the reference S/R pair. Overall, this study describes an innovative approach for RNA engineering and establishes that the KLI of the trans VS ribozyme can be adapted to cleave other folded RNA substrates.
嗜神经孢子菌VS核酶是一种催化性RNA,具有独特能力,可通过形成高度稳定的“亲吻环”相互作用(KLI)特异性识别并切割茎环底物。为了探索VS核酶切割其他底物的工程潜力,我们采用一种结合了理性和组合方法的创新工程方法,用其他已知的KLI替代野生型KLI。最初对蛋白质数据库进行了生物信息学搜索,以识别与VS核酶中发现的KLI结构相似的KLI。接下来,对包含这些替代KLI的底物/核酶(S/R)对进行了动力学和结构表征。有趣的是,尽管与参考S/R对相比活性有所降低,但所得的几个S/R对仍能以相当高的催化效率切割底物。总体而言,本研究描述了一种RNA工程的创新方法,并证实反式VS核酶的KLI可经改造以切割其他折叠的RNA底物。