High-throughput analysis of nucleic acid modification reactions using ion-pair reverse-phase high-performance liquid chromatography

被引:5
作者
Dickman, MJ [1 ]
Matin, MM [1 ]
Hornby, DP [1 ]
机构
[1] Univ Sheffield, Krebs Inst, Transgenom Res Lab, Sheffield S10 2TN, S Yorkshire, England
关键词
D O I
10.1006/abio.2001.5482
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ion-pair reverse-phase high-performance liquid chromatography is presented as a versatile platform for the rapid analysis of nucleic acid modification reactions in a high-throughput manner. This system allows both sensitive and nonradioactive assays to be developed for a variety of nucleic acid modification reactions. Examples presented here include assays for telomerase, uracil DNA glycosylase, polynucleotide kinase, T4 DNA ligase, C5-DNA methyltransferases, and the mismatch endonuclease CEL I. However, this approach is not confined to these reactions. Indeed the ability to perform a variety of nonradioactive assays with throughput times of 10 min per sample in conjunction with automated data analysis software represents a significant improvement in analytical and preparative nucleic acid enzymology. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:290 / 297
页数:8
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