Measurement of Single Macromolecule Orientation by Total Internal Reflection Fluorescence Polarization Microscopy

• Published in: Biophysical journal 2005-08, Vol.89 (2), p.1261-1271
• Main Authors: Forkey, Joseph N., Quinlan, Margot E., Goldman, Yale E.
• Format: Article
• Language: English
• Subjects: Actins - ultrastructure; Crystallography - instrumentation; Crystallography - methods; Equipment Design; Equipment Failure Analysis; Fluorescence; Imaging, Three-Dimensional - instrumentation; Imaging, Three-Dimensional - methods; Microscopy; Microscopy, Fluorescence - instrumentation; Microscopy, Fluorescence - methods; Microscopy, Polarization - instrumentation; Microscopy, Polarization - methods; Molecular biology; Molecules; Multiprotein Complexes - ultrastructure; Protein Conformation; Proteins; Spectroscopy, Imaging, Other Techniques
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1529/biophysj.104.053470

A new approach is presented for measuring the three-dimensional orientation of individual macromolecules using single molecule fluorescence polarization (SMFP) microscopy. The technique uses the unique polarizations of evanescent waves generated by total internal reflection to excite the dipole moment of individual fluorophores. To evaluate the new SMFP technique, single molecule orientation measurements from sparsely labeled F-actin are compared to ensemble-averaged orientation data from similarly prepared densely labeled F-actin. Standard deviations of the SMFP measurements taken at 40 ms time intervals indicate that the uncertainty for individual measurements of axial and azimuthal angles is ∼10° at 40 ms time resolution. Comparison with ensemble data shows there are no substantial systematic errors associated with the single molecule measurements. In addition to evaluating the technique, the data also provide a new measurement of the torsional rigidity of F-actin. These measurements support the smaller of two values of the torsional rigidity of F-actin previously reported.