蛋白质设计
计算机科学
无细胞蛋白质合成
功能(生物学)
蛋白质工程
蛋白质生物合成
蛋白质结构
生物
生物化学
酶
进化生物学
作者
Ella Lucille Thornton,Sarah Maria Paterson,Michael J. Stam,Christopher W. Wood,Nadanai Laohakunakorn,Lynne Regan
摘要
Abstract In protein design, the ultimate test of success is that the designs function as desired. Here, we discuss the utility of cell free protein synthesis (CFPS) as a rapid, convenient and versatile method to screen for activity. We champion the use of CFPS in screening potential designs. Compared to in vivo protein screening, a wider range of different activities can be evaluated using CFPS, and the scale on which it can easily be used—screening tens to hundreds of designed proteins—is ideally suited to current needs. Protein design using physics‐based strategies tended to have a relatively low success rate, compared with current machine‐learning based methods. Screening steps (such as yeast display) were often used to identify proteins that displayed the desired activity from many designs that were highly ranked computationally. We also describe how CFPS is well‐suited to identify the reasons designs fail, which may include problems with transcription, translation, and solubility, in addition to not achieving the desired structure and function.
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