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本文引用的文献

1
Primer release is the rate-limiting event in lagging-strand synthesis mediated by the T7 replisome.引物释放是由T7复制体介导的后随链合成中的限速事件。
Proc Natl Acad Sci U S A. 2016 May 24;113(21):5916-21. doi: 10.1073/pnas.1604894113. Epub 2016 May 9.
2
Quantitative full time course analysis of nonlinear enzyme cycling kinetics.非线性酶循环动力学的定量全时程分析
Sci Rep. 2013;3:2658. doi: 10.1038/srep02658.
3
A century of enzyme kinetic analysis, 1913 to 2013.一个世纪的酶动力学分析,1913 年至 2013 年。
FEBS Lett. 2013 Sep 2;587(17):2753-66. doi: 10.1016/j.febslet.2013.07.012. Epub 2013 Jul 12.
4
A novel non-radioactive primase-pyrophosphatase activity assay and its application to the discovery of inhibitors of Mycobacterium tuberculosis primase DnaG.一种新型非放射性引物酶-焦磷酸酶活性测定法及其在结核分枝杆菌引物酶 DnaG 抑制剂发现中的应用。
Nucleic Acids Res. 2013 Feb 1;41(4):e56. doi: 10.1093/nar/gks1292. Epub 2012 Dec 24.
5
Bacterial DNA replication enzymes as targets for antibacterial drug discovery.细菌 DNA 复制酶作为抗菌药物发现的靶标。
Expert Opin Drug Discov. 2012 Apr;7(4):327-39. doi: 10.1517/17460441.2012.660478. Epub 2012 Feb 21.
6
Mechanism of sequence-specific template binding by the DNA primase of bacteriophage T7.T7 噬菌体 DNA 引发酶序列特异性模板结合的机制。
Nucleic Acids Res. 2010 Jul;38(13):4372-83. doi: 10.1093/nar/gkq205. Epub 2010 Mar 28.
7
Fitting enzyme kinetic data with KinTek Global Kinetic Explorer.使用KinTek全球动力学探索器拟合酶动力学数据。
Methods Enzymol. 2009;467:601-626. doi: 10.1016/S0076-6879(09)67023-3.
8
Motors, switches, and contacts in the replisome.复制体中的马达、开关和触点。
Annu Rev Biochem. 2009;78:205-43. doi: 10.1146/annurev.biochem.78.072407.103248.
9
Primer initiation and extension by T7 DNA primase.T7 DNA 引发酶的引物起始与延伸
EMBO J. 2006 May 17;25(10):2199-208. doi: 10.1038/sj.emboj.7601112. Epub 2006 Apr 27.
10
Modular architecture of the bacteriophage T7 primase couples RNA primer synthesis to DNA synthesis.噬菌体T7引发酶的模块化结构将RNA引物合成与DNA合成偶联起来。
Mol Cell. 2003 May;11(5):1349-60. doi: 10.1016/s1097-2765(03)00195-3.

噬菌体T7复制蛋白在体外进行滞后链DNA合成的动力学

Kinetics of Lagging-strand DNA Synthesis In Vitro by the Bacteriophage T7 Replication Proteins.

作者信息

Hernandez Alfredo J, Richardson Charles C

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School;

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School.

出版信息

J Vis Exp. 2017 Feb 25(120):55312. doi: 10.3791/55312.

DOI:10.3791/55312
PMID:28287575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5409322/
Abstract

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.

摘要

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。