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利用荧光共振能量转移技术测量蛋白质使DNA弯曲的角度:以TBP结合TATA盒作为模型系统。

Using FRET to measure the angle at which a protein bends DNA: TBP binding a TATA box as a model system.

作者信息

Kugel Jennifer F

机构信息

Department of Chemistry and Biochemistry, University of Colorado at Boulder, 215 UCB, Boulder, Colorado 80309-0215.

出版信息

Biochem Mol Biol Educ. 2008 Sep;36(5):341-6. doi: 10.1002/bmb.20202.

Abstract

An undergraduate biochemistry laboratory experiment that will teach the technique of fluorescence resonance energy transfer (FRET) while analyzing protein-induced DNA bending is described. The experiment uses the protein TATA binding protein (TBP), which is a general transcription factor that recognizes and binds specific DNA sequences known as TATA boxes. When TBP binds to a TATA box, it bends the DNA. Such bending will be detected using FRET to measure the distance between two fluorophores located on the ends of the DNA. When TBP binds and bends the DNA, the fluorophores move closer together, reflected by an increase in FRET. At the completion of the experiment, three parameters will be determined: 1) the efficiency of the FRET, 2) the end-to-end distance between the fluorophores, and 3) the angle at which TBP bends the DNA. In performing this experiment, students will be introduced to FRET, gain experience in quantitative biophysical measurements, and appreciate how a protein can induce a dramatic change in DNA conformation.

摘要

本文描述了一个本科生物化学实验室实验,该实验在分析蛋白质诱导的DNA弯曲时教授荧光共振能量转移(FRET)技术。该实验使用蛋白质TATA结合蛋白(TBP),它是一种通用转录因子,可识别并结合称为TATA框的特定DNA序列。当TBP与TATA框结合时,它会使DNA弯曲。这种弯曲将通过FRET检测,以测量位于DNA末端的两个荧光团之间的距离。当TBP结合并使DNA弯曲时,荧光团会彼此靠近,这通过FRET的增加反映出来。实验完成时,将确定三个参数:1)FRET效率,2)荧光团之间的端到端距离,以及3)TBP使DNA弯曲的角度。在进行这个实验时,学生将接触到FRET,获得定量生物物理测量方面的经验,并了解蛋白质如何诱导DNA构象发生巨大变化。

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