无细胞蛋白质合成
计算生物学
蛋白质表达
溶解
蛋白质组学
模板
DNA
DNA微阵列
蛋白质微阵列
质粒
克隆(编程)
分子生物学
蛋白质生物合成
计算机科学
生物
基因表达
生物化学
基因
程序设计语言
作者
Song‐Min Schinn,Andrew Broadbent,William T. Bradley,Bradley C. Bundy
标识
DOI:10.1016/j.nbt.2016.04.002
摘要
A rapid, versatile method of protein expression and screening can greatly facilitate the future development of therapeutic biologics, proteomic drug targets and biocatalysts. An attractive candidate is cell-free protein synthesis (CFPS), a cell-lysate-based in vitro expression system, which can utilize linear DNA as expression templates, bypassing time-consuming cloning steps of plasmid-based methods. Traditionally, such linear DNA expression templates (LET) have been vulnerable to degradation by nucleases present in the cell lysate, leading to lower yields. This challenge has been significantly addressed in the recent past, propelling LET-based CFPS as a useful tool for studying, screening and engineering proteins in a high-throughput manner. Currently, LET-based CFPS has promise in fields such as functional proteomics, protein microarrays, and the optimization of complex biological systems.
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