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Using Three-color Single-molecule FRET to Study the Correlation of Protein Interactions
Published on: January 30, 2018
Four-color single-molecule fluorescence with noncovalent dye labeling to monitor dynamic multimolecular complexes
Vanessa DeRocco1, Trevor Anderson, Jacob Piehler
1Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. derie@unc.edu
Abstract:
To enable studies of conformational changes within multimolecular complexes, we present a simultaneous, four-color single molecule fluorescence methodology implemented with total internal reflection illumination and camera-based, wide-field detection. We further demonstrate labeling histidine-tagged proteins noncovalently with Tris-nitrilotriacetic acid (Tris-NTA)-conjugated dyes to achieve single molecule detection. We combine these methods to colocalize the mismatch repair protein MutSα on DNA while monitoring MutSα-induced DNA bending using Förster resonance energy transfer (FRET) and to monitor assembly of membrane-tethered SNARE protein complexes.
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