火球菌属
限制性酶
结扎测序
DNA
计算生物学
DNA测序
生物
限制地点
克隆(编程)
分子克隆
基因组DNA
多克隆站点
合成生物学
基因组文库
重组DNA
遗传学
分子生物学
计算机科学
基因
基序列
互补DNA
古细菌
程序设计语言
载体(分子生物学)
作者
Behnam Enghiad,Huimin Zhao
标识
DOI:10.1021/acssynbio.6b00324
摘要
Restriction enzymes are essential tools for recombinant DNA technology that have revolutionized modern biological research. However, they have limited sequence specificity and availability. Here we report a Pyrococcus furiosus Argonaute (PfAgo) based platform for generating artificial restriction enzymes (AREs) capable of recognizing and cleaving DNA sequences at virtually any arbitrary site and generating defined sticky ends of varying length. Short DNA guides are used to direct PfAgo to target sites for cleavage at high temperatures (>87 °C) followed by reannealing of the cleaved single stranded DNAs. We used this platform to generate over 18 AREs for DNA fingerprinting and molecular cloning of PCR-amplified or genomic DNAs. These AREs work as efficiently as their naturally occurring counterparts, and some of them even do not have any naturally occurring counterparts, demonstrating easy programmability, generality, versatility, and high efficiency for this new technology.
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