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Immobilized DNA hairpins for assay of sequential breaking and joining of DNA backbones.

作者信息

Scott Benjamin O S, Lavesa-Curto Manuel, Bullard Desmond R, Butt Julea N, Bowater Richard P

机构信息

School of Chemical Sciences and Pharmacy, University of East Anglia, Norwich NR4 7TJ, UK.

出版信息

Anal Biochem. 2006 Nov 1;358(1):90-8. doi: 10.1016/j.ab.2006.08.010. Epub 2006 Aug 23.

DOI:10.1016/j.ab.2006.08.010
PMID:16996469
Abstract

Immobilized DNA hairpins are exploited in a novel approach to assay DNA ligases and nucleases. A fundamental characteristic of the assay is that a fluorophore at the remote terminus of the hairpin reports on the integrity of the DNA backbone. The functionality of the protocol is confirmed using ATP- and NAD+-dependent DNA ligases and the nicking enzyme N.BbvCIA. The assay format is amenable to high-throughput analysis and quantitation of enzyme activity, and it is shown to be in excellent agreement with the more laborious electrophoretic approaches that are widely used for such analyses. Significantly, the assay is used to demonstrate sequential breaking and rejoining of a specific nucleic acid. Thus, a simple platform for biochemically innovative studies of pathways in cellular nucleic acid metabolism is demonstrated.

摘要

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Profiling the selectivity of DNA ligases in an array format with mass spectrometry.利用质谱技术对 DNA 连接酶进行阵列筛选以确定其选择性。
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