结晶
焦磷酸盐
DNA
成核
核糖核酸
化学
Crystal(编程语言)
水解
磷酸盐
镁
抄写(语言学)
生物物理学
体外
核酸
无机焦磷酸酶
结晶学
DNA合成
ATP水解
生物矿化
焦磷酸酶
核苷酸
组合化学
信使核糖核酸
生物化学
离子
纳米棒
作者
Soroush Ahmadi,Nathan Merica Stover,Krystian Ganko,Frances B. Kayser,Richard D. Braatz,Allan S. Myerson
标识
DOI:10.1021/acs.cgd.5c01710
摘要
mRNA-based vaccines and therapeutics are synthesized using the in vitro transcription (IVT) reaction. However, the byproduct pyrophosphate (PPi) forms insoluble magnesium pyrophosphate (Mg2PPi) during IVT, which coprecipitates with DNA, the transcription blueprint, interrupting the reaction and reducing RNA yield. The severity of this crystallization problem has prompted the routine inclusion of inorganic pyrophosphatase (PPase) in industrial processes to hydrolyze pyrophosphate into phosphate ions and prevent crystallization. To date, the mechanism by which Mg2PPi crystals interact with DNA has remained unclear. In this work, we demonstrate that DNA promotes Mg2PPi crystallization through a template-directed mechanism, reducing the nucleation induction time by a factor of 2. The resulting crystals form compact spherulites with a rosette habit, distinct from the morphologies observed in DNA-free systems. We propose that DNA preferentially templates the nucleation of Mg2PPi·3.5H2O crystals by interacting with the {100} crystal face. These findings reveal how DNA influences Mg2PPi crystallization and offer mechanistic insights relevant to optimizing RNA manufacturing systems.
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