Microscope and microscope observation method
View Patent ↗Provided is a microscope including: a scanner for scanning excitation light; an objective optical system that focuses the excitation light onto a sample and that collects fluorescence generated by the sample; a light-blocking member for transmitting a portion of the collected fluorescence; a detector for detecting the fluorescence; a setting unit that allows types of fluorescence having passed through the light-blocking member to be detected by the detector at different times in two types of positional relationships in which the positional relationship between the position of an opening in the light-blocking member and a focal point of the objective optical system in the sample is set to an optically conjugate positional relationship, in which in-focus fluorescence passes through the light-blocking member, and to an optically nonconjugate positional relationship; and an arithmetic operation unit for calculating the difference between fluorescence signals acquired at different times by the detector.
1. A microscope comprising:
a scanner for scanning excitation light from a light source;
an objective optical system that focuses the excitation light scanned by the scanner onto a sample and that collects fluorescence generated by the sample at each scanning position;
a light-blocking member that transmits a portion of the fluorescence collected by the objective optical system and that blocks another portion;
a detector for detecting the fluorescence having passed through the light-blocking member;
a setting unit that sets a positional relationship between the position of an opening in the light-blocking member and a focal point of the objective optical system in the sample to an optically conjugate positional relationship, in which in-focus fluorescence emitted from the focal point passes through the light-blocking member in an optical path from the sample to the detector, and to an optically nonconjugate positional relationship, in which the in-focus fluorescence does not pass through the light-blocking member, and that causes the detector to detect, at different times, types of fluorescence having passed through the light-blocking member in the set two types of positional relationships; and
an arithmetic operation unit for calculating the difference between fluorescence signals acquired by the detector at the different times.
2. The microscope according to claim 1 , wherein the setting unit relatively moves the position of the light-blocking member and the position of a fluorescence light beam that comes from the sample and that is incident upon the light-blocking member.
3. The microscope according to claim 2 , wherein the setting unit relatively moves, in a direction intersecting an optical axis of the fluorescence light beam, the position of the light-blocking member and the position of the fluorescence light beam incident upon the light-blocking member.
4. The microscope according to claim 3 ,
wherein the light source modulates the excitation light in an arbitrary repeated waveform, and
the setting unit includes a free-space optical system that splits the fluorescence collected by the objective optical system into a plurality of optical paths having different optical-path lengths and that causes the types of fluorescence to be incident upon different positions of the light-blocking member.
5. The microscope according to claim 3 ,
wherein the light source modulates the excitation light in an arbitrary repeated waveform, and
the setting unit includes a light-beam moving unit for moving the fluorescence light beam in a direction intersecting the optical axis thereof.
6. The microscope according to claim 5 , wherein the light-beam moving unit is a deflection element capable of changing a deflection angle.
7. The microscope according to claim 5 , wherein the light-beam moving unit is an acousto-optic element or an electro-optical element.
8. The microscope according to claim 3 , wherein the light-blocking member includes a plurality of pinholes arrayed in a direction intersecting the optical axis of the fluorescence light beam and is provided so as to be movable in the direction in which the pinholes are arrayed.
9. The microscope according to claim 2 , wherein the setting unit relatively moves, in the optical-axis direction of the fluorescence light beam, the position of the light-blocking member and an image-forming position of the fluorescence light beam incident upon the light-blocking member.
10. The microscope according to claim 9 ,
wherein the light source modulates the excitation light in an arbitrary repeated waveform, and
the setting unit includes a free-space optical system that splits the fluorescence collected by the objective optical system into a plurality of optical paths having different optical-path lengths and that causes the image-forming positions of the fluorescence light beam to differ.
11. The microscope according to claim 9 , wherein the setting unit is an acousto-optic lens capable of changing the image-forming position of the fluorescence light beam.
12. The microscope according to claim 1 ,
wherein the light source modulates the excitation light in an arbitrary repeated waveform,
the setting unit includes a plurality of optical fibers that allow the fluorescence collected by the objective optical system to be incident thereon and that have different lengths, and
the light-blocking member is formed by disposing incident ends of the types of fluorescence upon the optical fibers such that the incident ends are arrayed in a direction intersecting the optical axis of a fluorescence light beam from the sample.
13. The microscope according to claim 1 , wherein the arithmetic operation unit calculates the difference between two types of images generated by the fluorescence signals acquired by the detector in the two types of positional relationships set by the setting unit.
14. The microscope according to claims 1 , wherein the arithmetic operation unit calculates, for each pixel, the difference between the fluorescence signals acquired by the detector in the two types of positional relationships set by the setting unit.
15. A microscope observation method for focusing, onto a sample through an objective optical system, excitation light scanned by a scanner, collecting, with the objective optical system, fluorescence generated by the sample at each scanning position, and detecting, with a detector, fluorescence having passed through a light-blocking member, the method comprising:
a first step of detecting fluorescence with the detector in a state where the positional relationship between the position of an opening in the light-blocking member and the focal point of the objective optical system in the sample holds an optically conjugate positional relationship, in which in-focus fluorescence emitted from the focal point passes through the light-blocking member;
a second step of detecting fluorescence with the detector at a different time from a time in the first step in a state where the positional relationship between the position of the opening in the light-blocking member and the focal point of the objective optical system in the sample holds an optically nonconjugate positional relationship, in which the in-focus fluorescence does not passes through the light-blocking member; and
a third step of subtracting a fluorescence signal detected by the detector in the second step from a fluorescence signal detected by the detector in the first step.