Method for obtaining structural and functional information on proteins, based on polarization fluorescence microscopy
View Patent ↗The invention pertains to a method of obtaining structural and functional information on proteins, based on polarization fluorescence microscopy, which comprises subjecting a protein tagged with a fluorophore to two- or multi-photon fluorescence microscopy, whereas the observed protein is irradiated with a laser beam with light of at least two different polarizations, which excites the fluorescence of the fluorophore, and wherein information on localization, intensities and polarizations of the fluorescence excited by the different polarizations of the excitation laser beam is used to identify, localize and quantify anisotropy of absorption and/or fluorescence, which information is then used to infer structural and functional properties of proteins. An example of a device for obtaining structural and functional information on proteins, based on polarization fluorescence microscopy, comprises a modulator (P) for rapid modulation of the excitation beam ( 1 ) for eliciting two- or multi-photon fluorescence, and a control unit (R), wherein the function of the modulator (P) and control unit (R) is synchronized with scanning of the microscope (M) such that information on fluorescence intensity acquired by the microscope (M) is attributable to a particular polarization state of the excitation beam ( 1 ) by virtue of knowing the temporal profile of the polarization modulation of the excitation beam ( 1 ) effected by the modulator (P). The method and device of the invention allow determining and monitoring structure and function of proteins, such as membrane proteins, and thereby observing physiological processes in living cells.
1. A method of obtaining structural and functional information about an observed protein based on polarization fluorescence microscopy, the method comprising:
I) attaching a single fluorophore molecule to a protein to be observed,
II) subjecting the protein to be observed to two or multi-photon fluorescence microscopy, wherein the protein to be observed is irradiated by a laser beam with polarized light of at least two distinct polarizations, which excites fluorescence from the single fluorophore molecule,
III) observing at least one fluorescence signal from the single fluorophore molecule and collecting information on localization, intensity and/or polarization of the fluorescence signal excited by the different polarizations of the laser beam,
IV) observing and quantifying anisotropy of absorption based on the information on localization, intensity, and/or polarization of the fluorescence, and
V) identifying structural and functional properties of the observed protein based on the observed and quantified anisotropy of absorption.
2. The method of claim 1 , wherein the information on localization and intensities of fluorescence excited by different polarizations of the excitation laser beam is obtained in the form of a mixed image, containing in different parts fluorescence intensities excited by different polarizations of the excitation laser beam.
3. The method of claim 2 , wherein the processing of the mixed images comprises steps where
a) for each part of the mixed image, signal elicited by individual polarizations of the excitation beam is identified, and
b) for each of the used polarizations of the excitation laser beam, a separate image is created, containing signal excited by that polarization.
4. The method of claim 2 , wherein the different parts of the mixed image containing fluorescence intensities excited by different polarizations of the excitation laser beam are pixels.
5. The method of claim 4 , wherein two different polarizations of the laser beam light are used for excitation.
6. The method of claim 5 , wherein the excitation laser beam light polarizations are perpendicular to each other.
7. The method of claim 5 , wherein the mixed image contains in odd-numbered pixels intensities of fluorescence excited by one of the two polarizations used, and in even-numbered pixels intensities of fluorescence excited by the other of the two polarizations used.
8. The method of claim 5 , wherein the extent of anisotropic properties in individual pixels is determined by calculating the ratio of fluorescence intensity excited with one polarization of the excitation laser beam and fluorescence intensity excited with the other polarization of the excitation laser beam.
9. The method of claim 1 , wherein the observed protein is at least one of a membrane protein, a G-protein, a protein sensitive to calcium ion concentration, is a protein sensitive to membrane voltage, a receptor protein, an enzyme, a cytoplasmic protein, or a protein attached to the cytoskeleton.
10. The method of claim 1 , further comprising using the information on localization, intensity, and/or polarization of the fluorescence to identify and localize anisotropy of fluorescence.
11. The method of claim 10 , further comprising using the localization of anisotropy of fluorescence to identify structural and functional properties of observed protein.
12. The method of claim 9 , wherein the observed protein is in a living cell.