生物正交化学
麦克赫里
化学
靶蛋白
无细胞蛋白质合成
绿色荧光蛋白
生物化学
蛋白质生物合成
荧光
蛋白质纯化
组合化学
点击化学
基因
量子力学
物理
作者
Jaehyun Cha,Inchan Kwon
标识
DOI:10.1002/biot.201700739
摘要
Protein immobilization has been widely used for laboratory experiments and industrial processes. Preparation of a recombinant protein for immobilization usually requires laborious and expensive purification steps. Here, a novel purification‐free, target‐selective immobilization technique of a protein from cell lysates is reported. Purification steps are skipped by immobilizing a target protein containing a clickable non‐natural amino acid (p‐azidophenylalanine) in cell lysates onto alkyne‐functionalized solid supports via bioorthogonal azide‐alkyne cycloaddition. In order to achieve a target protein‐selective immobilization, p‐azidophenylalanine was introduced into an exogenous target protein, but not into endogenous non‐target proteins using host cells with amber codon‐free genomic DNAs. Immobilization of superfolder fluorescent protein (sfGFP) from cell lysates is as efficient as that of the purified sfGFP. Using two fluorescent proteins (sfGFP and mCherry), the authors also demonstrated that the target proteins are immobilized with a minimal immobilization of non‐target proteins (target‐selective immobilization).
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