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Quantifying transcription factor binding dynamics at the single-molecule level in live cells
- Source :
- CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET
- Publication Year :
- 2016
-
Abstract
- Progressive, technological achievements in the quantitative fluorescence microscopy field are allowing researches from many different areas to start unraveling the dynamic intricacies of biological processes inside living cells. From super-resolution microscopy techniques to tracking of individual proteins, fluorescence microscopy is changing our perspective on how the cell works. Fortunately, a growing number of research groups are exploring single-molecule studies in living cells. However, no clear consensus exists on several key aspects of the technique such as image acquisition conditions, or analysis of the obtained data. Here, we describe a detailed approach to perform single-molecule tracking (SMT) of transcription factors in living cells to obtain key binding characteristics, namely their residence time and bound fractions. We discuss different types of fluorophores, labeling density, microscope, cameras, data acquisition, and data analysis. Using the glucocorticoid receptor as a model transcription factor, we compared alternate tags (GFP, mEOS, HaloTag, SNAP-tag, CLIP-tag) for potential multicolor applications. We also examine different methods to extract the dissociation rates and compare them with simulated data. Finally, we discuss several challenges that this exciting technique still faces. Fil: Presman, Diego Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Fisiología, Biología Molecular y Neurociencias. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Fisiología, Biología Molecular y Neurociencias; Argentina. National Institutes of Health; Estados Unidos Fil: Ball, David A.. National Institutes of Health; Estados Unidos Fil: Paakinaho, Ville. National Institutes of Health; Estados Unidos Fil: Grimm, Jonathan B.. Howard Hughes Medical Institute; Estados Unidos Fil: Lavis, Luke D.. Howard Hughes Medical Institute; Estados Unidos Fil: Karpova, Tatiana S.. National Institutes of Health; Estados Unidos Fil: Hager, Gordon L.. National Institutes of Health; Estados Unidos
- Subjects :
- 0301 basic medicine
DYNAMICS
Microscope
Otras Ciencias Biológicas
Recombinant Fusion Proteins
Green Fluorescent Proteins
SINGLE-MOLECULE TRACKING
Nanotechnology
Computational biology
Plasma protein binding
Biology
General Biochemistry, Genetics and Molecular Biology
Article
law.invention
purl.org/becyt/ford/1 [https]
Ciencias Biológicas
03 medical and health sciences
Mice
Data acquisition
Receptors, Glucocorticoid
law
Cell Line, Tumor
Microscopy
Fluorescence microscope
Image Processing, Computer-Assisted
Animals
Humans
TRANSCRIPTION FACTOR
purl.org/becyt/ford/1.6 [https]
Molecular Biology
Transcription factor
Total internal reflection fluorescence microscope
DNA BINDING
FLUORESCENCE MICROSCOPY
Histocompatibility Antigens Class II
Epithelial Cells
Hep G2 Cells
Single Molecule Imaging
Antigens, Differentiation, B-Lymphocyte
Kinetics
030104 developmental biology
Gene Expression Regulation
GLUCOCORTICOID RECEPTOR
MCF-7 Cells
CIENCIAS NATURALES Y EXACTAS
Protein Binding
Subjects
Details
- ISSN :
- 10959130
- Volume :
- 123
- Database :
- OpenAIRE
- Journal :
- Methods (San Diego, Calif.)
- Accession number :
- edsair.doi.dedup.....96b43117eb174dcbc81a64b3fb076598