Hernandez Alfredo J, Richardson Charles C
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School;
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School.
J Vis Exp. 2017 Feb 25(120):55312. doi: 10.3791/55312.
Here we provide protocols for the kinetic examination of lagging-strand DNA synthesis in vitro by the replication proteins of bacteriophage T7. The T7 replisome is one of the simplest replication systems known, composed of only four proteins, which is an attractive feature for biochemical experiments. Special emphasis is placed on the synthesis of ribonucleotide primers by the T7 primase-helicase, which are used by DNA polymerase to initiate DNA synthesis. Because the mechanisms of DNA replication are conserved across evolution, these protocols should be applicable, or useful as a conceptual springboard, to investigators using other model systems. The protocols described here are highly sensitive and an experienced investigator can perform these experiments and obtain data for analysis in about a day. The only specialized piece of equipment required is a rapid-quench flow instrument, but this piece of equipment is relatively common and available from various commercial sources. The major drawbacks of these assays, however, include the use of radioactivity and the relative low throughput.
在此,我们提供了通过噬菌体T7的复制蛋白在体外对滞后链DNA合成进行动力学检测的实验方案。T7复制体是已知最简单的复制系统之一,仅由四种蛋白质组成,这对于生化实验来说是一个吸引人的特性。特别强调了T7引物酶 - 解旋酶合成核糖核苷酸引物的过程,DNA聚合酶利用这些引物来启动DNA合成。由于DNA复制机制在进化过程中是保守的,这些实验方案应该适用于使用其他模型系统的研究人员,或者作为一个概念性的跳板对他们有用。这里描述的实验方案高度灵敏,经验丰富的研究人员大约一天就能完成这些实验并获得用于分析的数据。唯一需要的专门设备是快速淬灭流动仪,但这种设备相对常见,可从各种商业渠道获得。然而,这些检测方法的主要缺点包括使用放射性以及相对较低的通量。