STEPPED BIOLOGICAL CHIP AND GENE SEQUENCING DEVICE FOR TESTING THE SAME

Abstract

A stepped biological chip and a gene sequencing device for testing same. The stepped biological chip comprises substrates and small small small small small small fluorescent balls carrying biological information arranged on the top of the substrates, and the heights of the center point of adjacent small small small small small small fluorescent balls from a substrate bottom edge A are incremented or decremented by equal value. The gene sequencing device comprises a chip placing platform, the stepped biological chip, and a microscope objective lens placed above the chip placing platform and an illumination light source irradiated on the stepped biological chip at a certain angle of incidence.

Claims

1. A stepped biological chip, comprising substrates and small fluorescent balls positioned at top ends of the substrates and carrying biological information, wherein vertical heights from centers of the small fluorescent balls to bottom edges A of the substrates ascend or descend by a constant.

2. The stepped biological chip according to claim 1, wherein a plurality of adjacent small fluorescent balls are arranged stepwise to form a group, and multiple groups of small fluorescent balls arranged stepwise are sequentially arranged on the biological chip.

3. A gene sequencing device for testing the stepped biological chip according to claim 1, comprising a chip placing platform and a stepped biological chip placed on the chip placing platform, and further comprising a microscope objective lens positioned above the chip placing platform and a light source irradiating the stepped biological chip at a certain incidence angle, wherein the stepped biological chip comprises substrates and small fluorescent balls positioned at top ends of the substrates and carrying biological information, and vertical heights from centers of the small fluorescent balls to bottom edges A of the substrates ascend or descend by a constant.

4. The gene sequencing device according to claim 3, wherein in each group of the small fluorescent balls arranged stepwise, a height difference between the adjacent small fluorescent balls is greater than twice a focal depth of the microscope objective lens.

5. The gene sequencing device f according to claim 3, wherein an angle between an incident light from the light source and the stepped biological chip is between 0° and 90°.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] FIG. 1 illustrates the schematic structure of a gene sequencing device according to the prior art.

[0016] FIG. 2 illustrates the schematic structure of the gene sequencing device according to the present invention.

[0017] FIG. 3 illustrates the schematic structure of the stepped biological chip according to the present invention.

DESCRIPTION OF THE EMBODIMENTS

[0018] The technical scheme of the present invention is further described below with reference to the drawings.

[0019] As shown in FIG. 3, the stepped biological chip of the present invention comprises substrates and small fluorescent balls fixed at top ends of the substrates and carrying biological information. The vertical heights from the centers of adjacent small fluorescent balls to bottom edges A of the substrates descend by a constant. Every five small fluorescent balls arranged stepwise form a group, and three such groups are sequentially arranged on the biological chip along the horizontal direction (three groups of small fluorescent balls are arranged in a horizontal line). In each group of small fluorescent balls arranged stepwise, the height difference between centers of adjacent small fluorescent balls is greater than twice the focal depth of the microscope objective lens.

[0020] The number of steps (the number of small fluorescent balls arranged stepwise in each group) and the step depth (the height difference between the centers of adjacent small fluorescent balls) is associated with the microscope objective lens used in the device. The microscope objective lens selected in this embodiment has a 5× magnification and an NA of 0.15. If a resolution of 0.9 μm (equivalent to a 20×/0.75 objective lens in conventional application) is required, 5 steps are needed since a 5× objective lens has a resolution of only 4.5 μm. That is, the number of small fluorescent balls arranged stepwise in each group is 5. In order to avoid interaction between images of two steps, the height difference between the two steps should be about 100 μm (twice the focal depth). Similarly, the testing speed of the gene sequencing device of the present invention will be greatly improved. The 5× objective lens has an object FoV of ø 5 mm (a standard objective lens with a field number of 25 mm), while the 20× objective lens used in conventional application has an object FoV of ø1.25 mm. Therefore, compared with the existing gene sequencing devices, the gene sequencing device of the present invention has a 16 times greater imaging area. Assuming that time consumed by chip moving, autofocusing and imaging remains constant and chips having the same area are detected, the gene sequencing device of the present invention has an 8 times faster testing speed.

[0021] As shown in FIG. 2, the gene sequencing device of the present invention for testing the aforementioned stepped biological chip comprises a chip placing platform and the stepped biological chip placed on the platform, and further comprising a microscope objective lens positioned above the platform and a light source irradiating the stepped biological chip at a certain angle of incidence. The angle of incidence, i.e. the angle between incident light and the biological chip, is between 0° and 90°. Specifically, when the microscope objective lens in the device is selected, the angle of incidence is greater than arctan(D/2L), wherein D is the diameter of the microscope objective lens, and L is the vertical distance from the objective lens to the biological chip.

[0022] The gene sequencing device of the present invention adopts the oblique illumination. The light that is not converted into fluorescence cannot enter the imaging system to cause background noise through mirror reflection, and thus an optical filter for blocking the light source is not needed in the device. Compared with the conventional coaxial illumination, oblique illumination greatly reduces the noise of the system, and the optical filter for blocking the light source is no longer needed, thereby greatly reducing the cost. The angle of oblique incidence is related to the outer diameter and working distance of the chosen objective lens. Assuming that the diameter of the objective lens is D and the working distance (vertical distance from the objective lens to the biological chip) is L, the angle of oblique incidence (a certain angle between incident light and the biological chip) of the light source should be greater than arctan(D/2L).

[0023] The workflow of the conventional method is as follows: the light is emitted from a light source, enters the system through reflection of a dichroic filter, then reaches the biological chip through a beam splitter and an objective lens, and irradiates biological tissues to excite fluorescence. The fluorescence is collected by the objective lens and enters a camera through the beam splitter, the dichroic filter, a tube lens and an optical filter. A high-precision X/Y-axis moving platform is required due to the big size of biological chip and small FoV of the objective lens. Autofocusing is performed once after each movement of the platform to ensure that the biological chip is always on the focal plane of the objective lens. Because the energy of the light source is very high while the energy of the fluorescence is extremely weak, an optical filter with a very high optical density is required to block the light reflected by the objective lens, the beam splitter and the like.

[0024] The workflow of the device of the present invention is as follows: the light from the light source obliquely enters the biological chip, but is regularly reflected by the substrates and the cover glass and does not enter the fluorescence collection system. Therefore, both the optical filter and the dichroic filter can be removed to greatly reduce the cost. Similarly, the excited fluorescence is captured by the camera through the objective lens and the tube lens, and enters. The autofocus module is also used to ensure that the biological chip is always on the focal plane of the objective lens when the X/Y moving platform moves. A plurality of images will be taken in a same FoV, and a displacement in the Z-direction is required between two adjacent images, wherein the depth of the displacement is the depth difference between two adjacent steps. Because of the large FoV of the microscope objective lens, all information on a biological chip can be obtained in one FoV. The device of the present invention only takes a certain number of images for the biological chip along the Z-direction corresponding to the number of steps (i.e., one imaging for each step). In existing devices, a biological chip is moved several times in the XY-direction to give all information on the biological chip in a similar area, and focusing is performed once after each movement. Thus, the testing speed of the device of the present invention is much faster than that of existing devices.