This preview shows pages 1–2. Sign up to view the full content.
This preview has intentionally blurred sections. Sign up to view the full version.View Full Document
Unformatted text preview: Investigating Transcriptional Regulation by Fluorescence Spectroscopy, from Traditional Methods to State-of-the-Art Single-Molecule Approaches S ILVIA Z ORRILLA , a , b M. P ILAR L ILLO , a D ENIS C HAIX , b E MMANUEL M ARGEAT , b C ATHERINE A. R OYER , b AND N ATHALIE D ECLERCK b a Instituto de Qu mica-F sica Rocasolano, CSIC, Madrid, Spain b INSERM (U554), Montpellier, France and Centre de Biochimie Structurale, CNRS (UMR5048), Universite Montpellier 1, Montpellier, France Gene expression regulation, in particular at the level of transcription, has been demonstrated to play a key role in the development of human diseases, including cancer, and in bacteria it is crucial for proliferation as well as for pathogenicity. Transcriptional regulation is based on complex networks of interactions, including those of the regulatory proteins with the operator DNAs, which are further modulated by ligands. Thus, understanding transcriptional regulation mechanisms requires a thorough analysis of the physical parameters underlying the interactions involved. Among the panoply of methods available, fluorescence spectroscopybased approaches have been widely used for the assessment of the thermodynamics and structural dynamics of biomolecular interactions. Here we will discuss the application of three fluorescence spectroscopy methods fluorescence anisotropy and fluorescence correlation and cross-correlation spectroscopyfor the investigation of proteinDNA, proteinprotein, and proteinligand interactions. The weaknesses and the strengths of each method will be highlighted on the basis of our experience in the analysis of the interactions of bacterial repressors implicated in transcriptional regulation in bacilli. Key words: fluorescence anisotropy; fluorescence correlation and cross-correlation spectroscopy; transcriptional regulation; biomolecular interactions Introduction Although virtually all steps from transcription initia- tion to protein degradation constitute potential targets for gene regulation, a critical level of control of gene ex- pression is the modulation of the transcription of DNA to messenger RNA. In bacteria, transcriptional regula- tion is crucial for proliferation and survival in response to the availability of nutrients 1 and, sometimes, it is de- cisive for the development of virulence. 2 On the other hand, defective control of transcriptional regulation of key genes has been shown to be at the basis of major human diseases, such as cancer and diabetes. 3 Hence, investigating the transcriptional regulation mechanism of selected genes will contribute to the identification of target interactions for pharmacological intervention....
View Full Document
- Spring '10