Yin Yipeng, Arneson Reed, Yuan Yinan, Fang Shiyue
Department of Chemistry,, and Health Research Institute, Michigan Technological University Houghton Michigan 49931 USA
College of Forest Resources and Environmental Science, Michigan Technological University Houghton Michigan 49931 USA
Chem Sci. 2024 Dec 18;16(4):1966-1973. doi: 10.1039/d4sc06958g. eCollection 2025 Jan 22.
The longest oligos that can be chemically synthesized are considered to be 200-mers. Here, we report direct synthesis of an 800-mer green fluorescent protein gene and a 1728-mer 29 DNA polymerase gene on an automated synthesizer. Key innovations that enabled this breakthrough include conducting the synthesis on a smooth surface rather than within the pores of traditional supports, and the use of the powerful catching-by-polymerization (CBP) method for isolating the full-length oligos from a complex mixture. Conducting synthesis on a smooth surface not only eliminated the steric hindrance that would otherwise prevent long oligo assembly, but also, surprisingly, drastically reduced synthesis errors. Compared with the benchmark PCR assembly gene synthesis method, the direct long oligo synthesis method has the advantages of higher probability to succeed, fewer sequence restrictions, and being able to synthesize long oligos containing difficult elements such as unusually stable higher-order structures, long repeats, and site-specific modifications. The method is expected to open doors for various projects in areas such as synthetic biology, gene editing, and protein engineering.
化学合成所能得到的最长寡核苷酸被认为是200聚体。在此,我们报告了在自动合成仪上直接合成800聚体绿色荧光蛋白基因和1728聚体29 DNA聚合酶基因。实现这一突破的关键创新包括在光滑表面而非传统载体的孔内进行合成,以及使用强大的聚合捕获(CBP)方法从复杂混合物中分离全长寡核苷酸。在光滑表面上进行合成不仅消除了否则会阻止长寡核苷酸组装的空间位阻,而且令人惊讶的是,还大幅减少了合成错误。与基准PCR组装基因合成方法相比,直接长寡核苷酸合成方法具有成功率更高、序列限制更少以及能够合成包含异常稳定的高阶结构、长重复序列和位点特异性修饰等困难元件的长寡核苷酸的优点。该方法有望为合成生物学、基因编辑和蛋白质工程等领域的各种项目打开大门。