DNA聚合酶
数字聚合酶链反应
计算机科学
DNA
聚合酶
DNA聚合酶Ⅱ
DNA钳
计算生物学
生物
聚合酶链反应
遗传学
基因
逆转录酶
作者
Xutong Liu,Kai Wen,E. K. C. Yu,Qixuan Zhao,Haoran Fu,Jingxuan Zhu,Haobo Han,Quanshun Li
出处
期刊:PubMed
日期:2025-07-16
卷期号:: e2500817-e2500817
标识
DOI:10.1002/smtd.202500817
摘要
DNA is increasingly recognized for its superior data storage density, favorable stability, and low energy requirements, positioning it as a potential alternative for future digital information storage systems. However, the replication and transfer of information within DNA is prone to errors, primarily due to the inaccuracy during DNA synthesis. Herein, 9°N DNA polymerase is explored from Thermococcus sp. 9°N-7 for robust DNA information storage, leveraging its thermophilic characteristics and error-correcting capability to facilitate high-fidelity DNA amplification. Notably, the enzyme demonstrate great improvement in managing DNA substitution errors compared to commercial DNA polymerases, effectively addressing the shortfall in substitution error correction typically presented in coding algorithms. This distinctive fidelity and substrate specificity of 9°N DNA polymerase is attributed to specific conformational changes and interactions during the process of nucleotide incorporation. Collectively, the findings suggested that integrating high-fidelity DNA polymerase with robust coding algorithm is a viable strategy to achieve error correction in DNA data storage. This combination exhibite the potential to augment the accuracy, portability, and scalability of DNA-based information storage systems, paving the way for reliable and effective data storage.
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