Methods for resolving positions in fluorescence stochastic microscopy using three-dimensional structured illumination
View Patent ↗Methods and systems to resolve positions of sample components in fluorescence stochastic microscopy using three-dimensional structured illumination microscopy (“3D-SIM”) are disclosed. In one aspect, components of a sample specimen are labeled with fluorophores and weakly illuminated with a frequency of light to stochastically convert a subset of the fluorophores into an active state. The sample is then illuminated with a three-dimensional structured illumination pattern (“3D-SIP”) of excitation light that causes the activated fluorophores to fluoresce. As the 3D-SIP is incrementally moved within the volume of the sample and images are recorded, computational methods are used to process the images to locate and refine the locations of the activated fluorophores thereby generating a super-resolution image of sample components.
1. A method for determining coordinate positions of light-emitting particles that label at least one component of a sample specimen using a light microscope, the method comprising:
activating a subset of the light-emitting particles by illuminating the sample with an activation light beam;
capturing a series of images of the light emitted from the subset of particles illuminated with an excitation light beam forming a three-dimensional structured illumination pattern;
generating a resolved image of the light-emitting particles from the series of images; and
repeatedly activating, capturing, and generating to obtain a number of resolved images that are processed to obtain a super-resolution image of the at least one component, wherein the super-resolution image has a higher resolution than a diffraction limit of the light microscope,
wherein illuminating the sample with the activation light beam further comprises illuminating the sample with the activation light beam that stochastically activates the subset of light-emitting particles, and
wherein generating the resolved image further comprises:
summing the series of images to generate a summed image of the each subset of particles;
determining centroid positions of the each subset of particles in the summed image; and
resolving centroid positions in the summed image to generate the resolved image.
2. The method of claim 1 , wherein capturing the series of images further comprises generating the illumination pattern from at least three beams of coherent excitation light transmitted through an objective lens to intersect within the sample.
3. The method of claim 1 , wherein capturing the series of images further comprises changing a position of the illumination pattern prior to capturing each image in the series.
4. The method of claim 3 , wherein changing the position of the illumination pattern further comprises rotating the illumination pattern.
5. The method of claim 3 , wherein changing the position of the illumination further comprises translating the illumination pattern.
6. The method of claim 1 , further comprises photobleaching the subset of light-emitting particles in the activated state.
7. The method of claim 1 , wherein generating the resolved image further comprises:
summing the series of images to generate a summed image of spots;
determining centroid positions of the spots; and
resolving spot centroid positions to generate the resolved image.
8. The method of claim 1 , further comprises discarding image data associated with inconsistent image results for single fluorophores.
9. The method of claim 1 , wherein the number of resolved images are processed to obtain the super-resolution image further comprising summing the resolved images to generate the super-resolution image.
10. The method of claim 1 , wherein each image of the series of images is identified by a lateral and an axial step the three-dimensional structured illumination is in at the time the each image is captured.
11. A method for generating a super-resolution image of a sample specimen using a light microscope, the method comprising:
separately activating different subsets of light-emitting particles attached to components of the sample by illuminating the sample with an activation light beam;
generating a series of images for each subset of activated particles by repeatedly illuminating the sample with an excitation light beam forming a three-dimensional structured illumination pattern and capturing an image of the light emitted from the subset of particles illuminated with the illumination pattern in different positions within the sample;
combining the series of images to generate a resolved image for each subset of particles; and
combining the resolved images to generate a super-resolution image of the sample, wherein the super-resolution image has a higher resolution than a diffraction limit of the light microscope,
wherein illuminating the sample with the activation light beam further comprises illuminating the sample with the activation light beam that stochastically activates the subset of light-emitting particles, and
wherein generating the resolved image further comprises:
summing the series of images to generate a summed image of the each subset of particles;
determining centroid positions of the each subset of particles in the summed image; and
resolving centroid positions in the summed image to generate the resolved image.
12. The method of claim 11 , wherein illuminating the sample with the excitation light beam forming a three-dimensional structured illumination pattern further comprises interfering at least three beams of coherent excitation light that passes through an objective lens to intersect within the sample.
13. The method of claim 11 , wherein capturing the image of the light emitted from the subset of particles illuminated with the illumination pattern in different positions further comprises rotating the illumination pattern.
14. The method of claim 11 , wherein capturing the image of the light emitted from the subset of particles illuminated with the illumination pattern in different positions further comprises translating the illumination pattern to a different lateral position for each image.
15. The method of claim 11 , wherein capturing the image of the light emitted from the subset of particles illuminated with the illumination pattern in different positions further comprises moving the illumination pattern to a different axial position for each image.
16. The method of claim 11 , further comprises photobleaching each subset of light-emitting particles in an activated state after each resolved image is generated.
17. The method of claim 11 , wherein generating the resolved image further comprises:
summing the series of images to generate a summed image of spots;
determining centroid positions of the spots; and
resolving spot centroid positions to generate the resolved image.
18. The method of claim 11 , further comprises discarding image data associated with inconsistent image results for single fluorophores.
19. The method of claim 11 , wherein combining the resolved images to generate the super-resolution image further comprising summing the resolved images.