Method and Arrangement for Light Sheet Microscopy
20170068080 · 2017-03-09
Assignee
Inventors
- Tiemo Anhut (Jena, DE)
- Thomas Kalkbrenner (Jena, DE)
- Daniel Schwedt (Weimar, DE)
- Jörg Siebenmorgen (Jena, DE)
- Helmut Lippert (Jena, DE)
Cpc classification
G02B21/365
PHYSICS
H04N25/71
ELECTRICITY
G02B21/006
PHYSICS
G02B21/367
PHYSICS
G02B21/008
PHYSICS
G02B27/0075
PHYSICS
G02B21/16
PHYSICS
International classification
G02B27/00
PHYSICS
Abstract
An arrangement for light sheet microscopy that includes a means for scanning a sample volume with a light sheet, which includes an angle 90 with the optical axis of an objective. The light sheet passes through the entire sample volume in the propagation direction, and the depth of field S.sub.obj of the objective is less than the optical-axis depth T of this sample volume. An optical device, disposed downstream of the objective, increases the depth of field S.sub.obj to a depth of field S.sub.effthe depth T of this sample volume. The arrangement also includes a means for positioning the sample volume within the region of the depth of field S.sub.eff. A spatially resolving optoelectronic area sensor is disposed downstream of the optical device, and hardware and software are provided to generate sample-volume images from the electronic image signals output by the area sensor.
Claims
1: A method for light sheet microscopy, comprising the following method steps: scanning a sample volume with a light sheet, which includes an angle 90 with an optical axis of an objective, wherein: the light sheet passes through the entire sample volume to be imaged in a propagation direction; and a depth of field S.sub.obj of the objective is less than a depth T of the sample volume in a direction of the optical axis; increasing the depth of field S.sub.obj in the detection beam path to a depth of field S.sub.eff that is greater than or equal to the depth T of the sample volume, and positioning the sample volume within the depth of field S.sub.eff; converting the optical image signals obtained with the increased depth of field S.sub.eff into electronic image signals with assignment to the regions of origin thereof in the sample volume; and generating images of the scanned sample volume from the electronic image signals.
2: The method for light sheet microscopy as claimed in claim 1; wherein scanning is carried out with a light sheet projected into the sample volume or generated by means of a point or line focus in scanning fashion.
3: The method for light sheet microscopy as claimed in claim 1; wherein two-dimensional or three-dimensional images of the scanned sample volume are generated according to an extended depth of field technique or a light-field technique.
4: The method for light sheet microscopy as claimed in claim 1; wherein, in a manner dependent on the sample volume to be scanned; a position of the light sheet in relation to the objective is varied in the x, y or z-direction; the angle is varied; a spatial extent of the light sheet within the sample volume is varied by rotation about the optical axis; or any combination of the above is performed.
5: The method for light sheet microscopy as claimed in claim 1; wherein the sample volume is scanned using a reflected-light method.
6: An arrangement for light sheet microscopy, comprising; a scanning means configured to scan a sample volume to be imaged with a light sheet, which includes an angle 90 with an optical axis of an objective, wherein: the light sheet passes through the entire sample volume to be imaged in a propagation direction; and a depth of field S.sub.obj of the objective is less than a depth T of the sample volume in a direction of the optical axis; an optical device, disposed downstream of the objective, configured to increase the depth of field S.sub.obj to a depth of field S.sub.eff that is equal to or greater than the depth T of the sample volume; a positioning means configured to position the sample volume within a region of the depth of field S.sub.eff; a spatially resolving optoelectronic area sensor disposed downstream of the optical device; and hardware and software, which are configured to generate images of the sample volume from the electronic image signals output by the area sensor.
7: The arrangement for light sheet microscopy as claimed in claim 6, further comprising: an optical means configured to: generate a light sheet scanned into the sample volume; and vary at least one of: a position of the light sheet in relation to the objective in the x, y, or z-direction; the angle ; and a spatial extent of the light sheet by rotation about the optical axis or about an axis parallel to the optical axis.
8: The arrangement as claimed in claim 6, further comprising: a common objective for illumination and detection purposes, wherein provision is made for shining illumination light into the entrance pupil of the objective at an entrance location offset parallel to the optical axis thereof; and a device configured to vary a direction for shining illumination light into the entrance pupil of the objective.
9: The arrangement for light sheet microscopy as claimed in claim 6; wherein the optical device comprises: an axicon; or a cubic phase mask; or a microlens array.
10: The arrangement for light sheet microscopy as claimed in claim 6; wherein a CCD sensor with a reception area aligned at right angles, at least substantially at right angles, to the detection beam path is provided as an area sensor.
11: The arrangement for light sheet microscopy as claimed in claim 6, further comprising: a means for changing the entrance location for shining illumination light into the entrance pupil of the objective, optionally in a decentralized or centralized manner in relation to the optical axis thereof.
12: The arrangement for light sheet microscopy as claimed in claim 11; wherein the optical image signals are obtained in a case of centrally shining the illumination light into the entrance pupil of the objective in accordance with confocal laser scanning microscopy.
13: The arrangement for light sheet microscopy as claimed in claim 6; wherein the hardware comprises: a personal computer (PC); and a means for electronic storage and visually perceivable reproduction of two-dimensional or three-dimensional images; and wherein the software comprises a predetermined algorithm for signal evaluation and for generating the two-dimensional or three-dimensional images.
14: The method for light sheet microscopy as claimed in claim 3; wherein the two- or three-dimensional images of the scanned sample volume are generated according to the extended depth of field technique or light-field technique with the insertion of diffractive optical elements (DOE) into the detection beam path.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF EMBODIMENTS
[0072] It is to be understood that the FIGS. and descriptions of the present invention have been simplified to illustrate elements that are relevant for a clear understanding of the present invention, while eliminating, for purposes of clarity, many other elements which are conventional in this art. Those of ordinary skill in the art will recognize that other elements are desirable for implementing the present invention. However, because such elements are well known in the art, and because they do not facilitate a better understanding of the present invention, a discussion of such elements is not provided herein.
[0073] The present invention will now be described in detail on the basis of exemplary embodiments.
[0074] The exemplary embodiment shown in
[0075] A laser light source 2, a beam widening optical unit 3 and a scanning device 4 generate an illumination beam path 5, which is deflected toward the objective 1 by means of the splitter surface 6 of a beam splitter 7 and which is shone with lateral offset from the optical axis 8 of the objective 1 into the entrance pupil 24 of the objective 1 (cf.
[0076] The illumination light being shone in a decentral manner in relation to the optical axis 8 causes the propagation direction of the light sheet 9 to include an angle 8 with the optical axis 8 which differs from 90. Here, the size of the angle is dependent on the distance between the entrance location 23 of the illumination light into the entrance pupil 24 and the optical axis 8.
[0077] A consequence of the light sheet 9 being at an angle relative to the optical axis 8 is that the light sheet 9 also illuminates regions of the sample volume 10 which lie at different depths in front of, and behind, the focal plane 11 in the axial direction, i.e. in the z-direction.
[0078] With the scanning movement in the x- and/or y-direction, the scanning device 4 prescribes the current position and alignment of the light sheet 9 within the sample volume 10. Said scanning device 4 is also embodied to rotate the light sheet 9 about an angle about the optical axis 8 or about an axis parallel to the optical axis 8 (cf.
[0079] Here, the scanning device 4 is embodied in an exemplary manner to [0080] change the distance between the entrance location 23 of the illumination light and the optical axis 8, [0081] displace the entrance location 23 in the pupil plane along a partial circle 25, the radius of which corresponds to the distance of the entrance location 23 from the optical axis 8, and to [0082] change the direction for shining the illumination light into the entrance pupil 24 of the objective 1.
[0083] However, the scope of the invention explicitly also includes each one of these functions being exercised by separate devices embodied therefor.
[0084] Reflected, scattered or excited light coming from the illuminated sample regions enters the objective 1 as detection light. The objective 1 forms a detection beam path 12, to which the splitter surface 6 is transparent, as depicted in
[0085] In the detection beam path, the axicon 19 is positioned between the two lens groups 15, 16a. The axicon 19 transforms the detection light into a Bessel-shaped light beam with a very long focus and therefore, according to the invention, brings about an increase in the nominal depth of field S.sub.obj of the objective 1 by a multiple to a depth of field S.sub.eff, as a result of which the whole sample volume 10 scanned by the light sheet 9 is imaged sharply on the reception plane 18.
[0086] A depth-resolved image of each illuminated thin section of the sample volume 10 is established by calculation from the intensity distribution in the detection beam path 12 registered by the area sensor 17 and said image is depicted in a manner that is visually perceptible by an observer. Such restoration methods are known per se. In the case of the so-called wavefront coding by means of phase masks, the data record is initially decoded numerically. This is carried out by a deconvolution with a known point spread function (PSF) determined by the mask, the objective and the microscope system. A projection of the sample volume along the optical axis is obtained after this first step. In a further step, the a priori information about the respectively current illumination geometry is included in the sample restoration in such a way that a unique spatial assignment of each detected event to the scanned sample volume is carried out.
[0087] As can be seen from
[0088] In a specific embodiment, the distance of the tube optical unit 13 from the position of the intermediate image 14 is f.sub.13=200 mm. Byway of example, the lens group 15 is at a distance of f.sub.15=200 mm from the position of the intermediate image 14 and generates an infinite beam path. The axicon 19 is at a distance of 41 mm from the lens group 15. The cone angle of the axicon 19 is 2; for example, it is 0.5 in this case. The distance between the axicon 19 and the reception plane 18 varies depending on the embodiment of the arrangement according to the invention; it can be up to 50 cm and is determined by the length of the Bessel beam which is generated by the axicon 19. The reception plane 18 is positioned in the region of the Bessel beam.
[0089] The lens groups 15, 16a can both consist of a plurality of lenses and be embodied as individual lenses. In principle, there is no need for a lens group 16a; the scope of the invention also includes an embodiment of the arrangement according to the invention without a lens or lens group 16a. However, a lens group 16a can advantageously be used to set optical parameters such as resolution and lateral magnification.
[0090]
[0091] The difference to the exemplary embodiment according to
[0092] The phase mask 20 transforms the detection light into an Airy-shaped light beam and likewise, according to the invention, brings about an increase in the nominal depth of field S.sub.obj of the objective 1 by a multiple to a depth of field S.sub.eff, as a result of which the whole sample volume 10 scanned by the light sheet 9 is also imaged sharply on the reception plane 18 in this case.
[0093] By applying the extended depth of field (EDoF) technology, a depth-resolved image of each illuminated thin section of the sample volume 10 is established in turn by calculation using the computing unit 26 from the intensity distribution in the detection light beam registered by the area sensor 17 and said depth-resolved image is depicted in a manner visually perceivable by an observer by means of the memory and reproduction unit 27.
[0094]
[0095] The exemplary embodiment according to
[0096] The microlens array 21 increases the depth of field S.sub.obj of the objective 1 by a multiple to a depth of field S.sub.eff by virtue of the sample volume 10 scanned by the light sheet 9 being imaged as a whole on the reception plane 18. Below, a three-dimensional reconstruction of this volume is undertaken by virtue of a depth-resolved image of the illuminated thin section being established by calculation by means of the light-field technology from the registered intensity distribution of the detection light beam and said depth-resolved image being depicted in a visually perceivable manner.
[0097] In the case mentioned here, obtaining and using the a priori information about the respectively current illumination geometry, as described further above on the basis of
[0098] Here too, two- or three-dimensional images of the scanned sample volume 10 are obtained by means of a computing unit 26.
[0099]
[0100] In a plan view of the entrance pupil 24 of an objective,
[0101] By contrast,
[0102] In both cases, this pupil illumination shows, in an exemplary manner, the generation of an inclined elliptic Gaussian light sheet.
[0103] As can be seen from
[0104] A variation of the distance of the entrance location 23 from the optical axis 8 brings about a change in the angle between the light sheet 9 and the optical axis 8. An adaptation of the position of the light sheet 9 to the sample volume 10 which extends in the x- and y-direction is achieved by changing the entrance angle of the illumination light into the pupil plane of the objective 1. A displacement of the focal plane 11 or of the region of the depths of the field S.sub.obj, S.sub.eff in the z-direction relative to the sample can be obtained by displacing the sample stage 22 in the z-direction.
[0105] In
[0106] Moreover, it is possible to identify from
[0107] This condition is also satisfied by the case L=T and therefore likewise lies within the scope of the invention.
[0108] Within the region L, the spatial extent of the light sheet 9 in the direction of the optical axis 8 does not exceed the value of e.g. 10 m and it is therefore suitable for detecting or measuring a sample volume 10 according to the principle of light sheet microscopy.
[0109] In conjunction with the change in the angle and the displacement of the light sheet 9 or the sample in the x- or y-direction, the depth of field S.sub.effT enables the detection and imaging of the entire sample volume 10.
[0110] While this invention has been described in conjunction with the specific embodiments outlined above, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art. Accordingly, the preferred embodiments of the invention as set forth above are intended to be illustrative, not limiting. Various changes may be made without departing from the spirit and scope of the inventions as defined in the following claims.
LIST OF REFERENCE SIGNS
[0111] 1 Objective [0112] 2 Laser light source [0113] 3 Beam widening optical unit [0114] 4 Scanning apparatus [0115] 5 Illumination beam path [0116] 6 Splitter surface [0117] 7 Beam splitter [0118] 8 Optical axis [0119] 9 Light sheet [0120] 10 Sample volume [0121] 11 Focal plane [0122] 12 Detection beam path [0123] 13 Tube optical unit [0124] 14 Intermediate image [0125] 15 Lens group [0126] 16 Lens group [0127] 17 Area sensor [0128] 18 Reception plane [0129] 19 Axicon [0130] 20 Phase mask [0131] 21 Microlens array [0132] 22 Sample stage [0133] 23 Entrance location [0134] 24 Entrance pupil [0135] 25 Partial circle [0136] 26 Computing unit [0137] 27 Memory and reproduction unit