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Development of a simple and versatile enzymatic DNA synthesis system that enables accurate, fast, and long oligos on demand

寡核苷酸 磷酰胺 DNA合成 组合化学 计算机科学 DNA 末端脱氧核苷酸转移酶 化学 材料科学 纳米技术 计算生物学 生物 生物化学 标记法 细胞凋亡
作者
Patrick Eimerman,Jeffrey A. Jeddeloh,Elise Champion,C. Peponnet,Sylvain Gariel,Xavier Godron,Thomas Ybert
摘要

Our novel, enzymatic DNA synthesis (EDS) technology was made through engineering of three critical components: a DNA polymerase, a solid support, and reversible terminators. Terminal deoxynucleotidyl-Transferase (TdT), which performs poly-nucleotide additions in a template-free manner, was engineered for improved expression, stability, and the ability to incorporate non-natural deoxynucleotide triphosphate bases. Novel surface chemistries have been developed to allow TdT to incorporate DNA bases on paramagnetic beads, resins, and glass as solid supports for EDS. Synthesis is enabled by the use of 3â€2-O-blocked reversible terminators, which suppresses poly-nucleotide addition by TdT until the 3'OH group on the extended polymer is deprotected. Here, we describe the development and key functionality of a benchtop EDS system for lab use. Unlike phosphoramidite synthesis, EDS produces DNA in the 'biological' orientation (i.e. 5'->3'), with an intact 5'-phosphate group. EDS provides a scalable synthesis system that eliminates the need for solvents, like acetonitrile, minimizing organic waste and decreasing research's carbon footprint, allowing users to make oligos without the need for specialized training and delivering oligos for iterative experiments without having to wait for a centralized oligo manufacturer. Current data indicates that purity levels comparable to those of existing technologies can be achieved, with an average per-position error rate <1%. For oligos up to 280nt long, we have demonstrated a cycle efficiency of 99.4%, which is greater than or equivalent to that of standard phosphoramidite synthesis. Using PCR, qPCR, dPCR, and sequencing assays we have demonstrated comparable performance to the same sequences synthesized using conventional chemistry. EDS is a disruptive technology that enables simple, robust systems capable of supporting same-day production of high quality, custom oligos. On-demand access to oligos revolutionize genomics research.

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