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增强型核酶催化的重组和寡核苷酸在肽-RNA 凝聚物中的组装。

Enhanced Ribozyme-Catalyzed Recombination and Oligonucleotide Assembly in Peptide-RNA Condensates.

机构信息

Biomimetic Systems, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.

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

出版信息

Angew Chem Int Ed Engl. 2021 Dec 6;60(50):26096-26104. doi: 10.1002/anie.202109267. Epub 2021 Nov 9.

Abstract

The ability of RNA to catalyze RNA ligation is critical to its central role in many prebiotic model scenarios, in particular the copying of information during self-replication. Prebiotically plausible ribozymes formed from short oligonucleotides can catalyze reversible RNA cleavage and ligation reactions, but harsh conditions or unusual scenarios are often required to promote folding and drive the reaction equilibrium towards ligation. Here, we demonstrate that ribozyme activity is greatly enhanced by charge-mediated phase separation with poly-L-lysine, which shifts the reaction equilibrium from cleavage in solution to ligation in peptide-RNA coaggregates and coacervates. This compartmentalization enables robust isothermal RNA assembly over a broad range of conditions, which can be leveraged to assemble long and complex RNAs from short fragments under mild conditions in the absence of exogenous activation chemistry, bridging the gap between pools of short oligomers and functional RNAs.

摘要

RNA 催化 RNA 连接的能力对其在许多前生物模型场景中的核心作用至关重要,特别是在自我复制过程中信息的复制。由短寡核苷酸形成的具有前生物合理性的核酶可以催化可逆的 RNA 切割和连接反应,但通常需要苛刻的条件或不寻常的情况来促进折叠并使反应平衡向连接方向移动。在这里,我们证明了核酶活性通过聚-L-赖氨酸介导的相分离得到了极大的增强,这将反应平衡从溶液中的切割转变为肽-RNA 共聚集物和共缩合物中的连接。这种分隔使在广泛的条件下进行稳健的等温 RNA 组装成为可能,这可以利用该特性在温和条件下从短片段组装长而复杂的 RNA,而无需外源激活化学物质,从而在短寡聚物库和功能 RNA 之间架起桥梁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bf4/9299051/086d5ed755ef/ANIE-60-26096-g002.jpg

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