Method and apparatus for illumination and detection in RESOLFT microscopy

Patent metadata

Field	Value
Publication number	US-9952155-B2
Application number	US-201213668414-A
Country	US
Kind code	B2
Filing date	Nov 5, 2012
Priority date	Nov 11, 2011
Publication date	Apr 24, 2018
Grant date	Apr 24, 2018

Abstract

A method for illumination and detection in RESOLFT microscopy using a pulsed or continuous light source for excitation light and switching light is characterized in that the excitation light ( 4 ) is irradiated in pulses and in that the pulse of the excitation light ( 4 ) is longer than 150 picoseconds, preferably up to a few hundred picoseconds, and even up to a few nanoseconds. A corresponding apparatus uses the method according to the present invention.

First claim

What is claimed is:

1. A Reversible Saturable Optical Fluorescence Transitions (RESOLFT) microscopy method comprising:
generating excitation light irradiated in light pulses of an illumination pattern of an excitation beam for a sample, using a first pulsed light source;
exciting a dye molecule within the sample to emit photons of emitted light in response to the excitation light;
generating switching light, using a second pulsed light source or a continuous light source to switch the dye molecule within the sample between at least two states; and
detecting the photons coming from the emitted light of the sample by way of applying at least one of optical filtering and temporal filtering,
wherein the first pulsed light source generates the excitation light with a pulse duration being longer than 150 picoseconds and shorter than a lifetime of an excited state of the dye molecule or shorter than 10 nanoseconds,
wherein in response to the switching light being irradiated in pulses from the second pulsed light source, no switching light is delivered to the sample during a light pulse of the excitation light and, during the light pulse of the excitation light, the photons emitted from the sample are rejected from detection and analysis, and upon or shortly after activation of a stimulation pulse, the photons emitted from the sample are detected and analyzed, or
wherein the switching light is irradiated continuously from the continuous light source, the stimulation pulse is delivered to the sample during the light pulse of the excitation light and, during the light pulse of the excitation light, the photons emitted from the sample are rejected as long as excitation light is irradiated, and upon or shortly after an end of the light pulse of the excitation light, the photons emitted from the sample are detected and analyzed.

2. The method as recited in claim 1 , wherein the light pulses of the excitation light have a pulse length ranging from 400 picoseconds to 10 nanoseconds.

3. The method as recited in claim 1 , wherein the pulse length of the excitation light corresponds approximately to a half-life of a fluorescent state of the dye molecule in the sample that is excited to emission by the excitation light.

4. A method as recited in claim 1 , the method further comprising:
irradiating the sample with pulsed switching light; and
rejecting the photons emitted from the sample from detection and analysis when no switching light is delivered to the sample during a light pulse of the excitation pulse;
wherein the step of detecting the photons emitted from the sample by way of applying at least one of optical filtering and temporal filtering further comprises detecting and analyzing the photons coming from the sample after activation of the stimulation pulse.

5. The method as recited in claim 4 , wherein the light pulse of the excitation light precedes light pulses of the switching light in time.

6. The method as recited in claim 5 , wherein the light pulse of the excitation light comprises an asymmetric time profile, and a falling edge of a light pulse intensity is steeper than a rising edge of the light pulse intensity.

7. The method as recited in claim 5 , wherein the light pulses of the switching light comprise an asymmetric time profile, and a rising edge of a light pulse intensity is steeper than a falling edge of the light pulse intensity.

8. The method as recited in claim 1 , wherein a light pulse of the switching light precedes the light pulses of the excitation light in time.

9. The method as recited in claim 8 , wherein the light pulse of the switching light comprises an asymmetric time profile wherein a rising edge of light pulse intensity is steeper than a falling edge of the light pulse intensity.

10. The method as recited in claim 8 , wherein the light pulses of the excitation light comprise an asymmetric time profile and an intensity with a steep falling edge and without a sharply rising edge.

11. A method as recited in claim 1 , further comprising:
irradiating the switching light continuously by the continuous light source and delivering the switching light to the sample during a light pulse of the excitation light; and
rejecting the photons emitted from the sample in response to the excitation light for detection as long as the excitation light is irradiated;
wherein the step of detecting the photons emitted from the sample by way of applying at least one of optical filtering and temporal filtering further comprises detecting and analyzing photons coming from the sample after an end of the light pulse of the excitation light.

12. The method of claim 1 , wherein RESOLFT microscopy comprises Stimulated Emission Depletion (STED) microscopy, Ground State Depletion (GSD) microscopy, Saturated Pattern Excitation Microscopy (SPEM), Saturated Structured Illumination Microscopy (SSIM) and upconversion microscopy.

13. The method of claim 1 , further comprising:
providing a detection beam of photons emitted from the sample along a detection beam path of a scanning microscope; and
filtering the detection beam by an optical filter positioned along the detection beam path to remove switching light reflected from the dye molecule, and portions of the excitation light located outside of the illumination pattern of the excitation beam.

Assignees

• Leica Microsystems

Inventors

• Foelling Jonas

Classifications

• G02B21/06

  Means for illuminating specimens · CPC title

• G01N21/6408 Primary

  with measurement of decay time, time resolved fluorescence · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G01N21/6458

  Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16) · CPC title