Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), Laval, QC, Canada.
Software Engineering and Computer Science Department, Concordia University, Montreal, QC, Canada.
Methods Mol Biol. 2021;2167:91-111. doi: 10.1007/978-1-0716-0716-9_7.
Pseudoknots are important motifs for stabilizing the structure of functional RNAs. As an example, pseudoknotted hammerhead ribozymes are highly active compared to minimal ribozymes. The design of new RNA sequences that retain the function of a model RNA structure includes taking in account pseudoknots presence in the structure, which is usually a challenge for bioinformatics tools. Our method includes using "Enzymer," a software for designing RNA sequences with desired secondary structures that may include pseudoknots. Enzymer implements an efficient stochastic search and optimization algorithm to sample RNA sequences from low ensemble defect mutational landscape of an initial design template to generate an RNA sequence that is predicted to fold into the desired target structure.
假结是稳定功能性 RNA 结构的重要基序。例如,与最小核酶相比,假结发夹核酶的活性更高。设计保留模型 RNA 结构功能的新 RNA 序列包括考虑结构中假结的存在,这通常是生物信息学工具的一个挑战。我们的方法包括使用“Enzymer”,这是一种用于设计具有所需二级结构的 RNA 序列的软件,其中可能包括假结。Enzymer 实现了一种有效的随机搜索和优化算法,用于从初始设计模板的低集合缺陷突变景观中对 RNA 序列进行采样,以生成预测为折叠成所需目标结构的 RNA 序列。