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An ultrasensitive site-specific DNA recombination assay based on dual-color fluorescence cross-correlation spectroscopy

机译:基于双色荧光互相关光谱的超灵敏位点特异性DNA重组测定

摘要

Site-specific exchange of genetic information is mediated by DNA recombinases, such as FLP or Cre, and has become a valuable tool in modern molecular biology. The so far low number of suitable recombinating enzymes has driven current research activities towards alteration of catalytic properties, such as thermostability or recognition sequences. However, identification and analysis of new mutants requires sensitive in vitro activity assays, which traditionally are based on gel electrophoresis. Here, we describe the development of a new sensitive DNA recombination assay based on dual-color fluorescence cross-correlation spectroscopy (DC-FCCS), which works in homogenous solution and does not require any separation step such as electrophoresis. The assay was validated with unlabeled FLP recombinase and different fluorescently labeled DNA substrates containing the FLP recognition target (FRT). This strategy fulfills all requirements for possible application in high throughput screening and engineering of new site-specific DNA recombinases starting from the FLP-FRT system, and is easily adjustable to other systems like Cre/loxP.
机译:DNA重组酶(例如FLP或Cre)介导了特定位置的遗传信息交换,已成为现代分子生物学中的一种有价值的工具。迄今为止,合适的重组酶的数量很少,从而驱使当前的研究活动转向改变催化性质,例如热稳定性或识别序列。但是,新突变体的鉴定和分析需要灵敏的体外活性测定,该测定传统上是基于凝胶电泳的。在这里,我们描述了一种基于双色荧光互相关光谱法(DC-FCCS)的新型敏感DNA重组检测方法的开发,该方法可在均质溶液中工作,不需要任何分离步骤(例如电泳)。用未标记的FLP重组酶和包含FLP识别靶标(FRT)的不同荧光标记的DNA底物验证了该测定法。该策略满足了从FLP-FRT系统开始在新的位点特异性DNA重组酶的高通量筛选和工程改造中可能应用的所有要求,并且可以轻松调整为Cre / loxP等其他系统。

著录项

  • 作者

    Jahnz Michael; Schwille Petra;

  • 作者单位
  • 年度 2005
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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