滚动圆复制
寡核苷酸
纳米技术
合成生物学
计算生物学
DNA
DNA合成
末端脱氧核苷酸转移酶
底漆(化妆品)
生物
化学
聚合酶
计算机科学
分子生物学
组合化学
遗传学
材料科学
有机化学
细胞凋亡
标记法
作者
Shuai Li,Wei Tan,Xuemei Jia,Qing Miao,Ying Liu,Dayong Yang
标识
DOI:10.1002/biot.202400026
摘要
Abstract Single‐stranded DNA (ssDNA) is the foundation of modern biology, with wide applications in gene editing, sequencing, DNA information storage, and materials science. However, synthesizing ssDNA with high efficiency, high throughput, and low error rate in vitro remains a major challenge. Various methods have been developed for ssDNA synthesis, and some significant results have been achieved. In this review, six main methods were introduced, including solid‐phase oligonucleotide synthesis, terminal deoxynucleotidyl transferase‐based ssDNA synthesis, reverse transcription, primer exchange reaction, asymmetric polymerase chain reaction, and rolling circle amplification. The advantages and limitations of each method were compared, as well as illustrate their representative achievements and applications. Especially, rolling circle amplification has received significant attention, including ssDNA synthesis, assembly, and application based on recent work. Finally, the future challenges and opportunities of ssDNA synthesis were summarized and discussed. Envisioning the development of new methods and significant progress will be made in the near future with the efforts of scientists around the world.
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