冷凝
肽
组合化学
溶剂
肽合成
相(物质)
蒸发
氨基酸
化学
过程(计算)
色谱法
材料科学
工艺工程
化学工程
计算机科学
有机化学
生物化学
工程类
物理
操作系统
热力学
作者
Jonathan M. Collins,Sandeep K. Singh,Travis A. White,Drew J. Cesta,Caroline Simpson,Levi J. Tubb,Christopher L. Houser
标识
DOI:10.1038/s41467-023-44074-5
摘要
We present a process for solid phase peptide synthesis (SPPS) that completely eliminates all solvent intensive washing steps during each amino acid addition cycle. A key breakthrough is the removal of a volatile Fmoc deprotection base through bulk evaporation at elevated temperature while preventing condensation on the vessel surfaces with a directed headspace gas flushing. This process was demonstrated at both research and production scales without any impact on product quality and when applied to a variety of challenging sequences (up to 89 amino acids in length). The overall result is an extremely fast, high purity, scalable process with a massive waste reduction (up to 95%) while only requiring 10-15% of the standard amount of base used. This transformation of SPPS represents a step-change in peptide manufacturing process efficiency, and should encourage expanded access to peptide-based therapeutics.
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