Singh K K, Rücker T, Hanne A, Parwaresch R, Krupp G
Institute for Hematopathology, University of Kiel, Germany.
Biotechniques. 2000 Aug;29(2):344-8, 350-1. doi: 10.2144/00292rr02.
Fluorescence polarization has been used recently to monitor diverse macromolecular interactions. In this report, the application of fluorescence polarization has been extended to monitor ribozyme reactions in real time. With fluorescently labeled substrate RNAs, group I ribozyme ligation and hammerhead ribozyme cleavage reactions were studied by fluorescence polarization in substrate excess (multiple turnover) conditions. These results also show that fluorescently labeled RNAs remain active substrates for ribozymes. Furthermore, a direct comparison of fluorescence polarization with fluorescence resonance energy transfer showed that both techniques were comparable for monitoring ribozyme reactions.
荧光偏振技术最近已被用于监测各种大分子相互作用。在本报告中,荧光偏振技术的应用已扩展到实时监测核酶反应。使用荧光标记的底物RNA,在底物过量(多轮反应)条件下,通过荧光偏振研究了I组核酶连接反应和锤头状核酶切割反应。这些结果还表明,荧光标记的RNA仍然是核酶的活性底物。此外,荧光偏振与荧光共振能量转移的直接比较表明,这两种技术在监测核酶反应方面具有可比性。