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II类内含子的计算从头设计产生高活性核酶。

Computational De Novo Design of Group II Introns Yields Highly Active Ribozymes.

作者信息

Szokoli Deni, Nwosu Noemi E, Glatt Lukas M, Mutschler Hannes

机构信息

Department of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn-Str. 4a, 44227, Dortmund, Germany.

出版信息

Chembiochem. 2025 Jul 18;26(14):e202500356. doi: 10.1002/cbic.202500356. Epub 2025 Jun 30.

Abstract

Group II introns (G2Is) are large self-splicing ribozymes with emerging potential in biotechnological applications. Despite growing interest, their complexity has so far precluded efforts to design them from scratch. While computational approaches have enabled the design of small RNA catalysts, methods for engineering large ribozymes remain underdeveloped. Herein, the RNA inverse folding algorithm aRNAque is used to design G2Is from scratch, yielding three novel self-splicing ribozymes with unusually stable structures. The designed intron Arq.I2 is revealed to be an unexpectedly proficient ribozyme in vitro, self-splicing at a rate comparable to the fastest known G2Is. While most G2Is are believed to be inactive under intracellular conditions in the absence of maturase proteins, it is shown that Arq.I2 self-splices in Escherichia coli cells. The results demonstrate that highly active variants of large and complex ribozymes can be designed de novo with relative ease using existing inverse folding algorithms, paving the way for the design of bespoke ribozymes derived from G2Is for the development of biotechnological tools.

摘要

II类内含子(G2Is)是大型自我剪接核酶,在生物技术应用中具有越来越大的潜力。尽管人们对此兴趣日增,但由于其复杂性,迄今为止尚无法从头开始设计它们。虽然计算方法已能设计小RNA催化剂,但用于工程化大型核酶的方法仍未充分发展。在此,RNA反向折叠算法aRNAque被用于从头设计G2Is,产生了三种具有异常稳定结构的新型自我剪接核酶。所设计的内含子Arq.I2在体外被证明是一种出人意料的高效核酶,其自我剪接速率与已知最快的G2Is相当。虽然大多数G2Is在没有成熟酶蛋白的情况下被认为在细胞内条件下是无活性的,但研究表明Arq.I2能在大肠杆菌细胞中自我剪接。结果表明,使用现有的反向折叠算法可以相对轻松地从头设计出大型复杂核酶的高活性变体,为设计源自G2Is的定制核酶以开发生物技术工具铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ce/12278348/ce168b6e5e92/CBIC-26-e202500356-g001.jpg

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