Kayedkhordeh Mohammad, Yamagami Ryota, Bevilacqua Philip C, Mathews David H
Department of Biochemistry and Biophysics and Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, USA.
Department of Chemistry, Pennsylvania State University, University Park, PA, USA.
Methods Mol Biol. 2021;2167:113-143. doi: 10.1007/978-1-0716-0716-9_8.
Ribozymes are RNAs that catalyze reactions. They occur in nature, and can also be evolved in vitro to catalyze novel reactions. This chapter provides detailed protocols for using inverse folding software to design a ribozyme sequence that will fold to a known ribozyme secondary structure and for testing the catalytic activity of the sequence experimentally. This protocol is able to design sequences that include pseudoknots, which is important as all naturally occurring full-length ribozymes have pseudoknots. The starting point is the known pseudoknot-containing secondary structure of the ribozyme and knowledge of any nucleotides whose identity is required for function. The output of the protocol is a set of sequences that have been tested for function. Using this protocol, we were previously successful at designing highly active double-pseudoknotted HDV ribozymes.
核酶是催化反应的RNA。它们存在于自然界中,也可以在体外进化以催化新的反应。本章提供了详细的方案,用于使用反向折叠软件设计一种核酶序列,该序列将折叠成已知的核酶二级结构,并通过实验测试该序列的催化活性。该方案能够设计包含假结的序列,这很重要,因为所有天然存在的全长核酶都有假结。起点是已知的含假结的核酶二级结构以及对功能所需的任何核苷酸身份的了解。该方案的输出是一组经过功能测试的序列。使用该方案,我们之前成功设计出了高活性的双假结丁型肝炎病毒核酶。