JP4577322B2 - Capillary array and cap set - Google Patents

Description

  The present invention relates to a capillary array used in a capillary array electrophoresis apparatus for separating and analyzing samples such as DNA and protein.

A technique is well known in which an array is configured by combining a plurality of capillaries, and an electrophoresis medium and a sample to be analyzed or separated are supplied to and moved to each capillary, and the target sample is used for separation and analysis. . A sample such as DNA or protein labeled with a fluorescent substance is supplied to the capillary. Such techniques are disclosed in US Pat. Nos. 5,366,608, 5,529,679, 5,516,409, 5,730,850, 5,790,727, 5,582,705, and 5,439,578.
, 5274240 and the like. From the viewpoint of separation / analysis throughput, there are many advantages of using a multicapillary rather than electrophoresis using a slab gel.

  Japanese Patent Application Laid-Open No. 9-96623 discloses a technique for separating and analyzing a fluorescently labeled sample by electrophoresis using a multicapillary array. The basic configuration of the capillary array electrophoresis apparatus includes an excitation optical system including a capillary array, a laser light source, and the like, a light receiving optical system for detecting fluorescence, a voltage application unit for electrophoresis, and the like. A capillary array has a structure in which capillaries are arranged in a plane, and a laser filled with a sample (fluorescent sample) labeled with a phosphor is irradiated from a direction parallel to the array surface of the capillaries. By condensing the laser, the fluorescent samples in all the capillaries are irradiated with the laser. The fluorescent sample irradiated with the laser emits fluorescence. This is a device for measuring a sample by detecting fluorescence from a fluorescent sample that emits light in a direction substantially perpendicular to the laser irradiation direction with a light receiving optical system.

  In this publication, the detection unit of the array is described in a schematic view, but the specific entire configuration of the capillary array to be incorporated in the electrophoresis apparatus is not described.

US Pat. No. 5,366,608 US Pat. No. 5,529,679 US Pat. No. 5,516,409 US Pat. No. 5,730,850 US Pat. No. 5,790,727 US Pat. No. 5,582,705 US Pat. No. 5,439,578 US Pat. No. 5,274,240 JP-A-9-96623

  An object of the present invention is to provide a specific capillary array configuration suitable for the capillary array electrophoresis apparatus.

  The present invention provides a capillary array including a light detection unit, a buffer solution injection unit, and a capillary head with a built-in electrode. The capillary array of the present invention has functions necessary for an electrophoresis apparatus.

  The present invention will be described in more detail. A plurality of capillaries having a polymer protective film on the surface, one end of which is bundled and the other end being widened, and the capillaries are arranged close to each other on a substantially flat surface to protect the polymer. The light detection unit from which the film has been removed, the above-described widened capillary, and a head with a built-in electrode, an electrode electrically connected to the head and immersed in the sample solution, and the bundle The present invention relates to a capillary array having the other electrode provided in the capillary.

  Further, according to another embodiment, one end of a plurality of capillaries having a protective coating is bundled, and the end portions thereof are smoothly aligned to form a buffer solution inlet, and the other end of the capillary is a capillary having an electrode built therein. The head is inserted into a metal tube electrically connected to the electrode through the head, and a light detection portion is formed in the middle portion of the capillary. The light detection portion removes the protective coating of the capillary, and the first The support substrate and the second support substrate are stacked to emit fluorescence from a window formed on one side of the substrate, and the surface opposite to the fluorescence emission side of the support substrate is painted black. A formed capillary array is provided.

  A groove through which laser light passes may be provided on one of the support substrates of the light detection unit of the capillary array, and the bottom surface thereof may be processed so as to reduce the reflection of fluorescence. The capillaries of the capillary head are cut out and inserted into the tube closely and fixed. The fixing method includes a method of injecting an adhesive and curing. By attaching a cap that protects the sample inlet, the capillary array can be transported, handled, and managed with peace of mind. In addition, drying of the open end of the capillary array during use interruption can be prevented. The capillary at the sample inlet is slightly protruded from the metal tube.

  In the light detection section, a reflected light shielding film is provided on the side opposite to the window that generates fluorescence to reduce noise. The sample supply part of the capillary array is provided with a metal tube electrode electrically connected to the electrode of the array head, and a capillary is inserted into this and fixed in the metal tube with an adhesive or the like.

  A cap capable of containing a buffer solution is attached to the tip of the sample supply unit to protect the tip of the sample supply unit during transportation. When a capillary array is installed in an electrophoresis device and used for separation and analysis, when the analysis is interrupted, a buffer can be placed in the cap to prevent the capillary tip from drying, so that the capillary can be reused at any time. Can be held in.

  According to the present invention, it is possible to provide a capillary array that is easy to handle, has sufficient mechanical protection, and can be easily attached to and detached from the electrophoresis apparatus.

  Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.

FIG. 1 is a schematic diagram when the capillary array of the present invention is applied to an electrophoresis system. A plurality of capillaries, for example, 16 are collected into one array. The light detection unit 29 is provided with a lower support plate a (glass substrate) and an upper support plate b (silicon substrate), and a portion made transparent by removing the polyimide coating of the capillary is provided in the window. FIG. 2 shows the overall structure of the capillary array of the present invention, which includes a capillary 1, a photodetection unit 29, a capillary head 30, and a built-in electrode load header 31. The tip of the capillary is inserted into the electrode tube 32 and fixed. The electrophoresis voltage is applied between the capillary head 30 and the load header 31.

In FIG. 1, a laser 33 generated by a laser light source 20 is divided into two by a beam splitter 22, and a traveling direction is changed by a mirror 21. The laser 33 is condensed by the condensing lens 23 and irradiates the capillary 1 from a direction parallel to the plane in which the capillary 1 is arranged. The inside of the capillary 1 is filled with a fluorescently labeled sample (fluorescent sample 34), and the fluorescent sample 34 emits fluorescent light 35 by irradiating the fluorescent sample 34 with the laser 33. The fluorescence 35 is detected by making the fluorescence 35 that emits light in a direction substantially perpendicular to the plane in which the capillaries 1 are arranged into parallel light by the first lens 24, dividing the image by the optical filter and the image dividing prism 25, and then the second lens 26. The image is formed on the CCD camera 27 and detected by the CCD camera 27, and the measurement data to be detected is processed by the processing arithmetic unit 28.

In FIG. 1, the laser 33 irradiates from both sides of the light detection unit 29, but it may be configured to irradiate only one side, and the light receiving optical system is not limited to the configuration shown in FIG. The number of capillaries 1 is not limited to 16, and the configuration of the buffer solution inlet 30 and the conductive fluorescent sample inlet 32 is not limited to the configuration shown in FIG.

  Subsequently, an operation procedure of the capillary array electrophoresis apparatus will be described. The buffer solution 36 contained in the buffer solution container 17 is injected into the capillary 1 from the buffer solution inlet 30. Next, the conductive fluorescent sample injection port 32 is put into the fluorescent sample container 18 filled with the fluorescent sample 34, and the fluorescent sample 34 is injected into the capillary 1. Thereafter, the conductive fluorescent sample inlet 32 is placed in a buffer container (not shown) containing a buffer solution, and a high voltage is applied between the buffer inlet 30 and the fluorescent sample inlet 31 by the high voltage power source 19. To cause electrophoresis. Since the migration speed of electrophoresis is proportional to the magnitude of the charge of the molecule and inversely proportional to the magnitude of the molecule, the fluorescent sample 34 is separated. Electrophoresis occurs for a long time by continuously applying a high voltage for a long time, and the fluorescence 35 emitted at this time is continuously measured.

  The detailed structure of the light detection unit is shown in FIG. In FIG. 3, the capillary array 1 provided with the removal portion 9 of the polyimide coating 10 is sandwiched between the glass substrate 3 and the silicon substrate 2. A groove through which laser light passes is formed in the glass substrate, and the bottom surface of the groove is ground glass 11. In addition, the laser non-irradiation part 5 is other than the groove part of the glass substrate.

  The silicon substrate 2 is provided with a window frame 7 having a window 6 for extracting fluorescence. A black coating 46 is formed on the outside of the glass substrate to reduce noise due to fluorescence reflection.

  FIG. 4 shows a cross section of the laser non-irradiation part 5 of FIG.

  The surface of the glass substrate 3 in contact with the polyimide coating is processed with a high degree of accuracy so that interference fringes can be observed, and the flatness is high. A plurality of capillaries are arranged in contact with the above-described highly flat surface via the polyimide resin 10. As a result, the plurality of capillaries follow the glass substrate 3 and can be arranged accurately and easily. A V-groove 8 is formed in the silicon substrate 2, and the capillaries are aligned in the groove.

FIG. 5 shows a cross section of the laser irradiation unit 4 of FIG. (A) is explanatory drawing when there is no black coating 46, (b) is explanatory drawing when the black coating 46 exists.

First, when there is no black coating 46 (a), the laser 47 passes through the plurality of capillaries arranged with high accuracy as described above. At this time, the scattered light 51 passes from the surface of the fused quartz tube 9 through the glass substrate 3 and is irradiated to the fluorescent material on the surface of the facing member 49 facing the glass substrate 3, and the emitted light 52 generated at that time returns to the fused quartz. Further, it passes through the through window 6 and goes to the first lens 24 to pick up noise. The same applies to the case where the fluorescent material 50 is attached to the back surface of the glass substrate 3 and causes noise.

However, as shown in (b), if the black coating 46 is applied to the back of the glass substrate 3, even if the fluorescence generating material 50 is present on the facing member, the fluorescence generating material adheres after the black coating 46 is further applied. However, the scattered light 51 is absorbed by the black paint 46 and the cause of noise is removed.

  Of course, the physical properties of the black paint 46 use a paint that does not generate fluorescence. A typical painting operation is a silk screen or the like. Of course, other printing methods may be used, and hand coating is sufficient.

  FIG. 6 schematically shows a representative plan view of FIG. 3 viewed from above. The silicon substrate 2 is indicated by a two-dot chain line. The through window 6 provided in the silicon substrate 2 is also indicated by a two-dot chain line. A state in which a plurality of capillaries are arranged is shown.

  The capillary alignment will be described with reference to FIG. The polyimide resin 10 covering the fused quartz tube 9 is removed only from the capillary of the light detection portion. Conventionally, this removal has been performed by removing a predetermined size separately for each piece and then aligning the removed portions. At this time, a processing error occurs in a predetermined removal width for every one, and the removal width varies. Further, alignment is performed so that the boundary (boundary where the polyimide resin 10 is cut) of the removed portion is aligned, but also alignment error occurs at this time, and much work time is required. Usually, it can be confirmed immediately because the boundary does not match. In the worst case, the polyimide resin can be seen from the through window 6, which greatly affects the detection.

  Therefore, without removing the coating for each one, after aligning the capillaries first and then removing the polyimide resin all at once, the removed portions of the polyimide resin 10 of the plurality of capillaries are neatly aligned. It can be confirmed immediately by the fact that the above-mentioned boundary portions are aligned. The predetermined width and the predetermined position of the removing portion can be freely changed together with a plurality of capillaries.

FIG. 7 is an explanatory diagram of a load header portion according to the embodiment of the present invention. The load header section includes a capillary 211, an electrode SUS pipe 212 as a metal tube, a holder 214, a holder cover 215, an electrode 216, and the like. The inside of the holder is assembled by welding a phosphor bronze electrode plate 216 through a SUS pipe 212. As shown in FIG. 7, the capillary 211 passes through the hole of the holder cover 215, passes through the SUS pipe, and projects slightly less than 1 mm to the opposite end surface of the SUS pipe.

The tips on the load header side of the 16 capillaries assembled with the capillary head and the fluorescence detection unit are trimmed to a length of L + 10 mm from the center of the fluorescence detection unit. Here, L is the capillary length from the center of the fluorescence detection section to the tip of the load header after the assembly of the load header is completed, and a predetermined length is required from the separation performance of the sequencer and the migration time.
, 500, 800 mm, etc. Next, the capillary 211 is passed through the SUS pipe 212 corresponding to each capillary from the hole of the load header cover 215. Then, with each capillary 211 adjusted so that it protrudes 10 mm from the tip of the SUS pipe 212, an adhesive is injected into the hole of the load header cover 215 to fix each capillary 211 to the load header cover 215.

Next, processing of the load header tip will be described. FIG. 8 is an enlarged sectional view showing the explanatory diagram. As shown in the drawing, an adhesive 217 is injected between the SUS pipe 212 and the capillary 211 to seal the gap between the SUS pipe 212 and the capillary 211. Thereafter, the tip of the capillary 211 is cut to a length of 0.5 to 1.0 mm from the end face of the SUS pipe 212 with a cutting device using a blade. By the above method, the lengths of the capillaries 211 from the load header tip to the fluorescence detection unit can be made uniform, and the migration time of the 16 capillaries 211 can be made uniform. Further, the structure in which the gap between the SUS pipe 212 and the capillary 211 is sealed is indispensable for preventing the sample liquid from entering the gap and preventing carryover when measuring another sample.

  Next, the length of the capillary 211 from the tip of the SUS pipe 212 needs to be 0.5 mm or more in order to form an optimum electric field for introducing DNA molecules into the capillary. On the other hand, as shown in FIG. 8, in order to measure a trace amount sample of about microliter, the tip length of the capillary 211 needs to be 1.0 mm or less. The length of 0.5 to 1.0 mm is also appropriate for the adhesive sealing work at the tip of the SUS pipe 212 and the cutting work at the tip of the capillary.

The tip shape of the SUS pipe 212 of the load header which is other embodiment of this invention is demonstrated. The overall structure is the same as that of the above embodiment, but a SUS pipe 212 having a shape in which the tip on the side incorporated in the holder is expanded on a cone is used. As a result, when the capillary 211 is inserted into the SUS pipe 212 from the hole of the load header cover 215, even if the concentricity of the two holes is slightly deviated, the capillary 211 can be easily inserted and the workability can be improved.

FIG. 9 is a perspective view showing the relationship between the sample injection portion of the capillary array and its protective cap in the present invention. The sample injection section at the tip of the load header 31 of the capillary array is configured to fit into the cap 341. As a result, it is possible to protect the capillary array during transportation, and when the operation of the electrophoresis apparatus is temporarily interrupted using the capillary array, or when the capillary array is removed from the electrophoresis apparatus for some reason and stored. The capillary array can be protected by putting a buffer solution or the like in the cap and immersing the capillary array in the cap so that the capillary tip does not dry. The flange part 134 of the cap 341 is in close contact with the load header 31.

  FIG. 10 is a view showing the relationship between the capillary head and its protective cap in the present invention. 30 is configured to fit a cap 111 made of silicon rubber. Thereby, similarly to the protective cap 341 in FIG. 9, protection during transportation of the capillary array can be achieved. Further, when the capillary array is detached from the electrophoresis apparatus and stored, drying of the tip of the capillary head can be prevented.

  The capillary 1 used in the capillary array described above uses a fused silica tube having an inner diameter of 50 ± 10 μm and an outer diameter of 340 ± 20 μm. Since the fused quartz tube itself is very fragile, a 15 ± 5 μm thick polyimide coating is applied. The inner diameter of the capillary is preferably thinner in consideration of the minute amount of the fluorescent sample 34. However, in order to suppress the concave lens effect due to the refractive index difference between the fluorescent sample 34 and the fused silica, it is better that the inner diameter is not too small. The inner diameter of the fused quartz tube is preferably 50 to 100 μm. The outer diameter is preferably thinner in order to suppress the influence of the difference in refractive index. However, since the outer diameter is difficult to be assembled due to static electricity, the outer diameter of the fused silica tube is preferably 250 to 350 μm.

  Further, the covering material for the capillary 1 is not limited to the polyimide resin 10, and a member having the same electrical insulating properties as the polyimide resin 10 and other characteristics may be used.

  As described above, the capillary array of the present invention has a basic function necessary for electrophoresis, which is a combination of the light detection unit, the voltage application unit, and the buffer solution gel supply unit that are necessary for incorporation into the electrophoresis apparatus. Capillary array.

It is the schematic which shows the electrophoresis system to which the capillary array of this invention is applied. It is a perspective view which shows the structure of the capillary array by this invention. It is an exploded view which shows the structure of the photon detection part of the capillary array by this invention. It is a schematic sectional drawing which shows the structure of the non-irradiation part of the photon detection part of the capillary array by this invention. It is a figure explaining the effect | action of the black painting in FIG. FIG. 4 is a plan view of FIG. 3. It is a partially cutaway perspective view showing the configuration near the load header. It is sectional drawing explaining the capillary tip specific structure. It is a perspective view explaining the relationship between a load header and a protective cap. It is a perspective view which shows the structure of a capillary head part.

Explanation of symbols

  DESCRIPTION OF SYMBOLS 1 ... Capillary, 2 ... Silicon substrate, 3 ... Glass substrate, 4 ... Laser irradiation part, 5 ... Laser non-irradiation part, 6 ... Through window, 7 ... Through window frame, 8 ... V groove, 9 ... Removal place, 10 ... Polyimide resin, 11 ... ground glass surface, 46 ... black paint, 212 ... SUS pipe.

Claims (1)

A plurality of capillaries having a sample injection end capable of injecting a sample and another end capable of injecting an electrophoretic medium; a holder portion for expanding and holding the sample injection end in the plurality of capillaries; and a plurality of excitation light irradiated A capillary array that can be attached to and detached from the electrophoretic device, including a photodetecting section that aligns a portion of the capillaries;
A cap having a container part capable of holding a buffer solution and a close contact part capable of being in close contact with the holder part;
A set of capillaries and caps that can be attached to the capillaries when the capillaries are removed from the electrophoresis apparatus and stored;
The contact portion is a set of a capillary array and a cap, which is a flange portion extending outward from the upper portion of the container portion .

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