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Dda 解旋酶紧密偶联单链 DNA 的移位与双链 DNA 的解旋:Dda 是一种最适活性的解旋酶。

Dda helicase tightly couples translocation on single-stranded DNA to unwinding of duplex DNA: Dda is an optimally active helicase.

机构信息

Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, 4301 West Markham Street, Slot 516, Little Rock, AR 72205, USA.

出版信息

J Mol Biol. 2012 Jul 13;420(3):141-54. doi: 10.1016/j.jmb.2012.04.007. Epub 2012 Apr 11.

DOI:10.1016/j.jmb.2012.04.007
PMID:22504228
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3372602/
Abstract

Helicases utilize the energy of ATP hydrolysis to unwind double-stranded DNA while translocating on the DNA. Mechanisms for melting the duplex have been characterized as active or passive, depending on whether the enzyme actively separates the base pairs or simply sequesters single-stranded DNA (ssDNA) that forms due to thermal fraying. Here, we show that Dda translocates unidirectionally on ssDNA at the same rate at which it unwinds double-stranded DNA in both ensemble and single-molecule experiments. Further, the unwinding rate is largely insensitive to the duplex stability and to the applied force. Thus, Dda transduces all of its translocase activity into DNA unwinding activity so that the rate of unwinding is limited by the rate of translocation and that the enzyme actively separates the duplex. Active and passive helicases have been characterized by dividing the velocity of DNA unwinding in base pairs per second (V(un)) by the velocity of translocation on ssDNA in nucleotides per second (V(trans)). If the resulting fraction is 0.25, then a helicase is considered to be at the lower end of the "active" range. In the case of Dda, the average DNA unwinding velocity was 257±42 bp/s, and the average translocation velocity was 267±15 nt/s. The V(un)/V(trans) value of 0.96 places Dda in a unique category of being an essentially "perfectly" active helicase.

摘要

解旋酶利用 ATP 水解的能量在 DNA 上移动的同时解开双链 DNA。根据酶是否主动分离碱基对,或只是隔离由于热磨损而形成的单链 DNA(ssDNA),将融解双链的机制分为主动或被动。在这里,我们表明 Dda 在 ssDNA 上单向迁移的速度与在集落和单分子实验中解开双链 DNA 的速度相同。此外,解旋速度对双链稳定性和施加的力基本不敏感。因此,Dda 将其所有的转位酶活性转化为 DNA 解旋活性,使得解旋速度受到转位速度的限制,并且酶主动分离双链。主动和被动解旋酶的特征是将每秒解开的碱基对的速度(V(un))除以每秒在 ssDNA 上的转位速度(V(trans))。如果得到的分数为 0.25,则认为解旋酶处于“主动”范围的低端。对于 Dda,平均 DNA 解旋速度为 257±42 bp/s,平均转位速度为 267±15 nt/s。V(un)/V(trans)的值为 0.96,这使得 Dda 属于一种独特的基本上是“完美”的主动解旋酶类别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e0/3372602/fc2f4086bab5/nihms374711f9.jpg
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