JPWO2017056274A1 - Cell analysis device and cell analysis method using the same - Google Patents

Abstract

An object of the present invention is to achieve both improvement in nucleic acid capture efficiency and improvement in cell capture efficiency in a single cell analysis apparatus. The present invention includes a plurality of cell capture units capable of capturing cells one by one, and a nucleic acid capture unit that exists corresponding to each cell capture unit and captures nucleic acid extracted from cells captured by the cell capture unit. The present invention relates to a device for single cell analysis provided with a two-dimensional array chip. The device of the present invention further includes a solution holding unit provided adjacent to the nucleic acid capturing unit of the two-dimensional array chip, and the solution holding unit absorbs the solution staying in the nucleic acid capturing unit due to capillary action and has a negative pressure. Has a three-dimensional porous body capable of discharging the solution absorbed by applying external pressure to the outside, and the solution holding part is adjacent to the flow path, and the negative pressure is applied to one end of the flow path to hold the solution. And a nucleic acid capturing part and a cell capturing part are configured to be capable of applying a negative pressure.

Description

  The present invention relates to technical fields such as gene expression analysis, cell function analysis, biological tissue analysis method and disease diagnosis, and drug discovery, and more specifically, a cell analysis apparatus capable of gene analysis of a single cell and the same The present invention relates to a cell analysis method using.

  In the research on the practical application of regenerative medicine, the research on diagnostic methods related to cancer and immunity by genetic analysis, or the basic research on the life phenomenon of multicellular organisms, not only the average gene expression level but also the organization The importance of quantitatively analyzing the contents of individual cells has begun to be emphasized. Therefore, it is desired to take out cells one by one and monitor the expression levels of various genes quantitatively. If single-cell analysis can be performed to measure the level of gene mRNA that is active in living tissue at the single-cell level, various phenomena occurring in the body, including the interaction between cells, can be known in detail. Therefore, it is expected to have a great effect on research and diagnosis in the life science field, especially in the medical or drug discovery field.

  Single cell analysis is a technique for detecting and quantifying biomolecules in cells for each single cell with high accuracy. For single cell analysis, cells are isolated for individual processing, nucleic acids to be measured in cells are efficiently extracted, cDNA is synthesized (reverse transcription), and PCR amplification is performed as necessary. It is necessary to analyze the sequence of the resulting product.

  In Patent Document 1, individual cells are captured in the pores of the pore array sheet, and then the nucleic acids of the cells are captured by a DNA probe fixed to the pores and having a different tag sequence for each pore to synthesize cDNA. Thus, a device capable of obtaining a product for sequence analysis that can identify individual cells is disclosed. FIG. 1 shows a basic configuration of such a device (corresponding to FIG. 8 of Patent Document 1).

  In the device of FIG. 1, a cell solution containing cell 1 is introduced from inlet 6. In order to fill the upper region 4 of the porous membrane 2 with the cell solution, the cell solution is sucked from the upper outlet 7. When a negative pressure is applied by sucking the solution from the lower outlet 8, the cell solution is sucked through the porous membrane 2, and the cell 1 is guided to the cell trap 3. The cell 1 is captured by the lattice-shaped cell trap 3 built on the porous membrane 2, and when the cell is disrupted, the mRNA in the cell is fixed in the porous membrane directly under the cell. Captured by

  When a device such as that shown in FIG. 1 is used, a nucleic acid extracted from captured cells can be captured with little contact with a region other than the inner wall of the porous membrane, which is a reaction region, and cDNA can be synthesized. Therefore, it is possible to prepare a product for sequence analysis with high efficiency while suppressing the probability that a nucleic acid is adsorbed on the inner wall of a device not related to the reaction.

International Publication No. 2014/020657

  In the device as shown in FIG. 1, in order to efficiently capture nucleic acids, the average diameter of the pores constituting the porous membrane 2 needs to be several μm or less, and particularly preferably 1 μm or less. The film thickness of the porous membrane 2 is desirably 10 μm or more, particularly several tens of μm or more. However, when such a porous membrane is used, the pressure loss when passing the cell solution increases. When the pressure loss is large, the suction speed is reduced when the solution is sucked from the lower outlet 8, so that the speed at which the cells 1 are sucked into the cell trap 3 is lowered. For this reason, a phenomenon has been observed in which a relatively large number of cells settle by gravity and remain in the region on the other device before reaching the cell trap 3. In FIG. 1, a cell indicated by 9 is an example of a cell that has not reached such a cell trapping unit 3.

  The remaining of cells other than the cell trapping part 3 not only reduces the percentage of cells that can be analyzed, but also causes associated problems. That is, when extracting nucleic acid from a cell, a step of crushing the cell is required. At that time, cells existing in a region other than the cell capturing unit 3 are also crushed at the same time, and a plurality of nucleic acids extracted from the cell are extracted. Into the cell trapping part 3, and the problem that accurate single cell analysis becomes difficult occurs.

  The above problems are caused by an increase in pressure loss due to an increase in nucleic acid capture efficiency, a decrease in the diameter of the pores of the porous membrane 2 and an increase in the film thickness. Therefore, it is an essential problem that there is a trade-off relationship between improvement in nucleic acid capture efficiency and improvement in cell capture efficiency.

  As a result of studying the problems as described above, the present inventors have used a three-dimensional porous body that can absorb a solution by capillary action and discharge it by applying a negative pressure. It was found that both the capture efficiency and the cell capture efficiency can be improved. The gist of the present invention is as follows.

(1) It has a plurality of cell capture units that can capture cells one by one and a nucleic acid capture unit that exists corresponding to each cell capture unit and captures nucleic acid extracted from the cells captured by the cell capture unit. A device for analyzing a single cell with a two-dimensional array chip,
A solution holding unit provided adjacent to the nucleic acid capturing unit of the two-dimensional array chip; and the solution holding unit absorbs a solution staying in the nucleic acid capturing unit by capillary action and applies a negative pressure. It has a three-dimensional porous body that can discharge the solution absorbed by
The device is configured such that the solution holding unit is adjacent to the flow channel, and can apply a negative pressure to the solution holding unit, the nucleic acid capturing unit, and the cell capturing unit by applying a negative pressure to one end of the flow channel. .
(2) The flow path communicates with an intake port opened to the outside of the device, and external air is taken in from the intake port by applying a negative pressure to one end of the flow path, and the airflow passes through the solution holding unit. The device according to (1), wherein the solution is discharged from the solution holding unit.
(3) The device according to (2), comprising a plurality of two-dimensional array chips and a solution holding unit corresponding to each two-dimensional array chip, wherein the flow path connects the plurality of solution holding units in series. .
(4) A plurality of two-dimensional array chips and a solution holding unit corresponding to each two-dimensional array chip are provided, the flow path connects a plurality of solution holding units in parallel, and the intake port is an individual solution. The device according to (2), wherein a plurality of devices are provided for each holding unit.
(5) The device according to any one of (1) to (4), wherein the absorption time of the liquid droplets when 1 μL of pure water is dropped on the surface of the three-dimensional porous body is within 10 seconds.
(6) The device according to any one of (1) to (4), wherein the three-dimensional porous body is a porous glass material, a glass fiber aggregate, or a glass bead aggregate.
(7) The nucleic acid capture unit has a nucleic acid probe for capturing a nucleic acid, the nucleic acid probe hybridizes with a nucleic acid extracted from a cell, and a different cell recognition sequence corresponding to each cell capture unit The device according to any one of (1) to (4).
(8) The device according to (7), wherein the nucleic acid capturing unit has a structure filled with beads to which a nucleic acid probe is immobilized.
(9) A single cell analysis method using the device according to (1) or (2), wherein the two-dimensional array chip is filled with a cell solution, and the flow path adjacent to the solution holding unit Including applying a negative pressure to one end of the cell trapping portion to apply a negative pressure to the cell trapping portion to absorb the cell solution into the solution holding portion and adsorbing a single cell to the cell trapping portion, Method.
(10) The method further includes a step of crushing a single cell adsorbed on the cell trapping part in a state where a negative pressure is applied to the cell trapping part and causing the nucleic acid trapping part to capture a nucleic acid extracted from the cell. The analysis method according to (9).
(11) A second nucleic acid probe having a sequence that hybridizes with the nucleic acid captured by the nucleic acid capture unit, and an enzyme and a substrate for synthesizing a complementary strand using the captured nucleic acid as a template are supplied to the nucleic acid capture unit. The method for analysis according to (10), further comprising a step of performing complementary strand synthesis.

  The device for single cell analysis of the present invention has succeeded in improving the efficiency of capturing cells by the cell capture unit while maintaining the nucleic acid capture efficiency in the nucleic acid capture unit. As a result, it has become possible to prepare a sample for single cell analysis with higher efficiency than conventional devices.

FIG. 2 is a diagram showing a basic configuration of a device described in Patent Document 1, which is a related technique of the present invention. It is a figure showing one mode of composition of a cell analysis device concerning the present invention. FIG. 3 is a diagram showing an outline of the configuration of a device manufactured in Example 1-1. FIG. 3 is a graph showing the result of comparing the suction speed of a solution in the device according to the present invention shown in FIG. 2 and the device according to the prior art as shown in FIG. FIG. 4 is a flowchart showing details of a single cell analysis method using the device of the present invention produced in Example 1-1 shown in FIG. FIG. 4 is a flowchart showing details of a single cell analysis method using the device of the present invention produced in Example 1-1 shown in FIG. FIG. 4 is a flowchart showing details of a single cell analysis method using the device of the present invention produced in Example 1-1 shown in FIG. It is a figure explaining the adjustment procedure of the sample for sequencing. FIG. 6 is a diagram illustrating an outline of a configuration of a device according to Example 2. FIG. 5 is a diagram showing an example of the configuration of an apparatus that can automatically execute sample preparation, including a device according to Example 2. FIG. 6 is a diagram illustrating an outline of a configuration of a device according to Example 3. FIG. 6 is a diagram showing another aspect of the configuration of the device according to Example 3. FIG. 6 is a diagram illustrating an outline of a configuration of a device according to Example 4.

  FIG. 2 is a diagram showing an embodiment of the configuration of the cell analysis device according to the present invention, in which (a) is a top view, (b) is a cross-sectional view in the 2A-2A ′ cross section, and (c) is 2B-2B ′. Sectional drawing in a cross section is shown, respectively.

  The cell analysis device according to the present invention includes a plurality of cell capture units 203 capable of capturing cells one by one, and nucleic acids that are present corresponding to each cell capture unit and extracted from the cells captured by the cell capture unit. A two-dimensional array chip having a nucleic acid capturing unit 202 for capturing is provided, and a liquid holding unit 211 is provided adjacent to the nucleic acid capturing unit 202 of the two-dimensional array chip. Further, the solution holding unit 211 is adjacent to the flow channel, and is sucked from the lower outlet 208, which is one end of the flow channel, so that the solution holding unit 211, the nucleic acid capturing unit 202, and the cell capturing unit 203 are connected via the flow channel. Is configured to be able to apply a negative pressure. In the embodiment shown in FIG. 2, an intake port 213 opened to the outside is further provided in the flow path.

  The nucleic acid capturing unit 202 is composed of a porous material, beads (preferably magnetic beads), or the like, and a nucleic acid probe for capturing nucleic acids extracted from cells is fixed. The nucleic acid probe has a nucleic acid capture sequence that hybridizes with a nucleic acid extracted from a cell and a different cell recognition sequence corresponding to each cell capture portion, and amplifies the nucleic acid captured by such a nucleic acid probe. Single cell analysis becomes possible by using the obtained product.

  Cell solution is introduced from the upper inlet 206. Similar to the conventional example shown in FIG. 1, the cell solution is sucked from the upper outlet 207 in order to fill the upper region 204 with the cell solution. Next, the point that a single cell is adsorbed to the cell trap 203 by sucking the solution from the lower outlet 208 and applying a negative pressure is the same as the conventional example. However, the apparatus according to the present invention is different from the conventional apparatus in that the solution holding unit 211 is provided immediately below the nucleic acid capturing unit 202 made of a porous membrane or beads.

  The solution holding part 211 is composed of a three-dimensional porous body, and the three-dimensional porous body quickly absorbs the aqueous solution contacted by capillarity, and the absorbed aqueous solution is not exposed to the nucleic acid capturing part 202, in particular. It has the property that it can be discharged. By discharging the absorbed aqueous solution, the solution absorption performance by the capillary phenomenon of the three-dimensional porous body can be maintained. By utilizing the capillary phenomenon of the three-dimensional porous body, the solution staying in the nucleic acid capturing unit 202 is sucked more quickly than in the case of simply applying a negative pressure as in the conventional example shown in FIG. In addition, the ability of the cell capture unit 203 to adsorb cells can be improved.

  The three-dimensional porous material used in the present invention has pores of several tens to several hundreds of nanometers at random, and has surface hydrophilicity that can absorb an aqueous solution by capillary action caused by the presence of the pores. It is the material which has. Specific examples thereof include a porous glass material, a glass fiber aggregate (for example, a bundle of glass fibers aligned in the same direction), and a glass bead aggregate (with an average particle size in the range of 0.1 to 30 μm). Preferred). It is preferable that the three-dimensional porous body is not easily deformed because the absorbed solution is unlikely to be unintentionally discharged and flows back to the nucleic acid capturing unit 202 or the cell capturing unit 203. The hydrophilicity of the surface of the three-dimensional porous body has a water contact angle measured using pure water of 90 ° or less, preferably 80 ° or less, more preferably 50 ° or less, particularly preferably 40 ° or less, Alternatively, when 1 μL of pure water is dropped onto a three-dimensional porous body having a volume sufficient to hold 1 μL of liquid, it is within 10 seconds, preferably within 5 seconds, more preferably within 3 seconds, particularly preferably. It can be characterized by any of the absorption of drops dropped within 1 second. In addition, that the droplet is absorbed by the three-dimensional porous body means that the presence of the droplet cannot be visually confirmed when observed from a plane perpendicular to the surface of the three-dimensional porous body. To do.

  The three-dimensional porous body constituting the solution holding unit 211 preferably has a pore diameter sufficiently larger than the pore diameter of the pores of the nucleic acid capturing unit 202 made of a porous membrane or beads, for example, the average pore diameter. It is preferably 0.2 μm or more, particularly 1 μm or more. With such a size, an excessively large pressure loss does not occur when a gas such as air passes through the solution holding unit 211. If the pore diameter of the pores of the three-dimensional porous material is as described above, a sufficient pressure difference is generated between the upper and lower portions of the nucleic acid capturing unit 202 when negative pressure is applied from the lower outlet 208. Can be made. Further, the three-dimensional porous body constituting the liquid holding unit 211 may be composed of a porous body having a plurality of pore diameters. In particular, when the pore diameter of the porous body in the portion adjacent to the nucleic acid capturing section 211 is made smaller than the area away from the nucleic acid capturing section 211, the absorption capacity (capillary effect) due to capillary action of the porous body is improved, and the porous body It is possible to improve the speed of discharging the solution held in the material by air pressure.

  It is preferable that the flow path provided with the solution holding part 211 and communicated with the lower outlet 208 is also communicated with the intake port 213 opened to the outside of the apparatus via the pressure adjusting member 212. In the apparatus of FIG. 2, the intake port 213 is released to the outside in the upper part direction of the apparatus. In the case where the intake port 213 is provided, when negative pressure is applied from the lower outlet 208, outside air is taken in from the intake port 213 via the pressure adjusting member 212, and an air flow 214 is generated, whereby the solution holding unit 211 is obtained. The solution absorbed in is discharged. By providing the intake port 213, the solution holding unit 211 absorbs the solution by capillary action only when negative pressure is applied from the lower outlet 208, that is, the volume of the solution discharged by the solution holding unit 211. Only by capillary action can the solution be absorbed again. In addition, in the case of a configuration in which the intake port 213 is not provided, there is a case where the solution does not reach the solution holding unit 211 and absorption does not start just by filling the upper region 204 with the solution, whereas if absorption starts, the solution holding unit Absorption does not stop until the capacity of 211 is satisfied and the controllability becomes insufficient, but the controllability can be supplemented by providing the intake port 213. It is preferable to further provide an air valve in the intake port 213 because the controllability of solution absorption is further improved.

  The pressure adjusting member 212 is preferably a member that causes a larger pressure loss when the gas passes than when the solution passes through the nucleic acid capturing unit 202. By providing such a pressure adjusting member 212, when negative pressure is applied from the lower outlet 208, sufficient negative pressure is applied not only to the intake port 213 but also to the solution holding unit 211, the nucleic acid capturing unit 202, and the cell capturing unit 203. Is applied. As the pressure adjusting member 212, for example, a material having pores finer than the holes of the nucleic acid capturing unit 202, for example, about 1/5 to about 1/10 of the average pore diameter of the holes of the nucleic acid capturing unit 202, more preferably about If a material having an average pore diameter of 1/7 to about 1/9, specifically about 1/8 is used, it can be said that the balance is good from the viewpoint of the difference in viscosity between air and water.

  After adsorbing the cells to the cell trapping part 203 as described above, if the cells are disrupted with a lysis buffer or the like while a negative pressure is applied from the lower outlet 208, the nucleic acid (mRNA) extracted from the cells becomes nucleic acid Captured by the nucleic acid probe fixed to the capture unit 202. The captured nucleic acid is added to the nucleic acid capturing unit 202, a second nucleic acid probe having a sequence that hybridizes with the nucleic acid (for example, a poly T sequence), an enzyme for synthesizing a complementary strand using the captured nucleic acid as a template, and It can be amplified by supplying a substrate and carrying out complementary strand synthesis to obtain a sample for analysis. In addition, although amplification of nucleic acid assumes PCR amplification, it is not limited to it, You may use other amplification methods, such as rolling circle amplification (RCA), NASBA, and LAMP method. When the nucleic acid capturing unit 202 is composed of magnetic beads, nucleic acid amplification may be performed after the magnetic beads are taken out from the two-dimensional array chip.

  EXAMPLES Hereinafter, although this invention is demonstrated in detail using an Example, this invention is not limited to these Examples.

Example 1-1 Device Manufacturing FIG. 3 is a diagram showing an outline of the configuration of a device manufactured in this example, (a) is a top view, (b) is a cross-sectional view in the 3A-3A ′ cross section Indicates. The device 301 includes a plurality of reaction chambers 302, and each of the reaction chambers 302 includes a plurality of cell traps 203 and a two-dimensional array including nucleic acid traps 202 corresponding to the individual cell traps 203. A chip 315 is disposed. The cell solution is supplied onto the two-dimensional array chip 315 by flowing through the common channel 305 from the upper inlet 307 toward the upper outlet 308, and the chip is filled with the cell solution. The individual inlet 311 is used when a reagent including a primer having a tag sequence for identifying a chip is specifically introduced when a reagent is individually introduced into a chip.

  In the production of the two-dimensional array chip 315, a resin chip made of dimethylpolysiloxane (PDMS) obtained by injection molding (a square with a side of 1.125 mm) is used, and a through hole having a diameter of about 3 to 10 μm smaller than a cell is formed. Thus, a cell trap 203 was obtained. The two-dimensional array chip may be manufactured using a resin chip obtained by injection molding using another resin (polycarbonate, cyclic polyolefin, polypropylene, etc.), or using a nanoimprint technology or a semiconductor process. Can also be done. The material used for manufacturing the two-dimensional array chip is preferably a hydrophobic material.

A cylindrical space having a diameter of several tens of μm was provided immediately below the cell trapping part 203, and magnetic beads with a nucleic acid trapping probe fixed therein were filled therein to constitute the nucleic acid trapping part 202. The filling of magnetic beads is performed individually using an ink jet printer head. In a state where the chip is turned upside down, 2 nL of the bead solution in which different sequences are fixed for each region is individually filled in the nucleic acid capturing unit 202. In the bead solution used for filling, magnetic beads having a diameter of 1 μm are suspended at a number density of 5 × 10 ⁹ particles / mL. Streptavidin is immobilized on the magnetic beads, and a 5 ′ biotin group-modified DNA probe is immobilized via the streptavidin. In order to improve the nucleic acid capture efficiency by increasing the number of magnetic beads to be filled, the bead diameter was set to several μm or less. A bead outflow prevention membrane (resin porous membrane having a pore diameter of 0.8 μm: Isopore membrane, manufactured by Millipore) having a pore diameter smaller than the bead diameter was adhered to the two-dimensional array chip 315 so that the filled magnetic beads did not flow out.

  A porous shirasu sintered body (shirasu porous glass: SPG film, manufactured by SPG Techno Co.), which is a three-dimensional porous body, is disposed in the lower flow path 309 of the nucleic acid capturing unit 202 to form a solution holding unit 211. The lower flow path 309 communicates with the lower outlet 310 and the intake port 319 for taking in air, and in the vicinity of the intake port 319, the pressure adjustment filter 320 (in this embodiment, taking into account the difference in viscosity between water and air, A resin porous membrane (Isopore membrane, manufactured by Millipore) having a pore diameter of 0.1 μm and an air valve 318 were provided. When cells are captured by the cell capturing unit 203, the two-dimensional array chip 315 is filled with a cell solution, and then a negative pressure is applied by a syringe pump connected to the lower outlet 310 with the air valve 318 opened. In addition, it can replace with a syringe pump and can also use other pumps, such as a diaphragm pump.

  Since the nucleic acid capture unit 202 of the 2D array chip 315 is filled with fine magnetic beads, the cell solution does not flow at a sufficient flow rate by simply applying a pressure difference between the upper and lower parts of the 2D array chip 315. Thus, the cells cannot be efficiently captured by the cell capturing unit 203. However, in the device of this example, by adopting the above-described configuration, the flow rate of the cell solution can be increased by utilizing the capillary phenomenon in the three-dimensional porous body, and the cell capture efficiency can be improved. .

  In the device shown in FIG. 3, position A (upper part of the two-dimensional array chip 315), position B (lower flow path 309 between the solution holding unit 211 and the pressure adjustment filter 320), position C (two The pressure relationship between the three-dimensional array chip 315 and the solution holding unit 211) and the position D (the lower flow path 309 closer to the lower outlet 310 than the solution holding unit 211) is A >> B> C> D. With this setting, the nucleic acid capturing unit 202 is filled with the solution, and the solution comes into contact with the solution holding unit 211. Capillary phenomenon occurs in the three-dimensional porous body constituting the solution holding unit 211, and a large suction force is generated. Occur. For example, when the pore size of the three-dimensional porous material is 10 μm, the suction force due to this capillary phenomenon generates a suction force of about 100 kPa in the cell trapping portion 203 (assuming a circular shape with a diameter of 5 μm) in the configuration of this example. Can be calculated. In addition, by using two SPG membranes with a pore size of 2 μm and a SPG membrane with a pore size of 10 μm (both 0.6 mm thick) as a three-dimensional porous body, the suction pressure is increased to 500 kPa, and the three-dimensional porous membrane It was possible to hardly cause a decrease in flow rate when the solution was discharged by air. Furthermore, it was confirmed that the same effect can be obtained by packing silica (glass) beads having a diameter of 10 μm to 100 μm in a liquid holding part to obtain a three-dimensional porous body.

  The air taken in from the suction port 319 passes through the solution holding part 211 due to the pressure difference between the position B, the position C, and the position D, whereby the aqueous solution absorbed by the solution holding part 211 is discharged toward the position D. The By this discharge, the suction force due to the capillary action of the solution holding unit 211 is recovered, so that the suction force of the solution holding unit 211 is maintained as long as the suction from the lower outlet 310 continues. On the other hand, when the suction from the lower outlet 310 is stopped, the inner wall of the three-dimensional porous body constituting the solution holding part 211 is quickly covered with the aqueous solution, and the suction force is lost.

Example 1-2 Single Cell Analysis Method Using Device FIGS. 5 to 7 show details of a single cell analysis method using the device of the present invention produced in Example 1-1 shown in FIG. FIG. In this example, (1) cell capture, (2) cell lysis (crush), (3) reverse transcription (cDNA synthesis), (4) RNA degradation, (5) 2nd strand synthesis, (6) PCR amplification Run in. Steps (4) to (4) may be performed in the device, and then the two-dimensional array chip may be placed in a separate reaction tube to perform the reactions (5) and (6). Here, the case where the reactions (1) to (6) are performed in the device will be described.

  First, a process of capturing cells in the cell solution by the cell capturing unit 203 on the two-dimensional array chip 315 is performed. For this purpose, the cell solution is introduced from the upper inlet 307 and sucked from the upper outlet 308 to fill the two-dimensional array chip 315 with the cell solution. Next, the air valve 318 is opened. Next, by applying a negative pressure to the lower outlet 310 using a syringe, the pressure distribution at positions A to D becomes A >> B> C> D from the higher pressure, and the cell solution becomes the two-dimensional array chip 315. The cells are captured by the cell capturing unit 203 after passing through the upper cell capturing unit 203 and the nucleic acid capturing unit 202. 300 in FIG. 3 indicates a cell captured by the cell capturing unit 203.

  In order to disrupt the cells, a lysis buffer is introduced from the upper inlet 307 and aspirated from the upper outlet 308, so that the lysis buffer fills the two-dimensional array chip and negative pressure is applied to the lower outlet 310 to obtain the required aspiration rate. Apply pressure. The relative value of the pressure distribution is almost the same as that during cell capture. In this example, the syringe position was not changed from cell aspiration, and the negative pressure of the lower outlet 310 was set to be almost the same as that during cell capture. At this time, care was taken not to make the pressure in the lower outlet 310 positive. This is because, when the pressure in the lower outlet 310 becomes positive, the cell solution flows backward through the cell trap 203 and the trapped cells 300 are released.

  Next, the process proceeds to the reverse transcription (cDNA synthesis) step. Reset the negative pressure value to achieve the required rate of introduction of the reverse transcription reagent mix. After the setting, a reverse transcription reagent is introduced from the upper inlet 307, and the two-dimensional array chip 315 is filled with the reagent. Thereafter, the temperature of the device is raised to proceed with the reverse transcription reaction and maintained for the time required for the reaction. Further, the temperature is raised to 85 ° C. for inactivating the reverse transcriptase. In order to wash and discharge unnecessary washing liquid, the washing buffer is introduced from the upper inlet 307, and the negative pressure is reset to introduce and remove the washing buffer from the nucleic acid capturing unit. The next steps, mRNA degradation and 2nd strand synthesis, are almost the same as the reverse transcription step.

  The last step is PCR amplification. The PCR reagent mix is introduced into the upper inlet 307, and the negative pressure is set so that the PCR reagent mix is introduced into the nucleic acid capturing unit 202 at a necessary solution speed. Start the temperature cycle to perform the PCR reaction, and change the pressure setting to stop solution introduction in the first to several cycles. Thereafter, the temperature cycle is repeated until the required PCR product concentration is reached, and in order to collect the PCR product, a negative pressure is applied to the lower outlet 310, suction is performed, and the collected PCR product solution is discharged into a tube.

  Next, a procedure for adjusting a sequencing sample using the two-dimensional array chip 315 will be described in detail. FIG. 8 shows how the sample is prepared by processing the mRNA captured by the nucleic acid capturing unit 202 of the device of this example. This step involves nucleic acid extraction from each cell and capture of nucleic acid (mRNA) (step 1), cDNA synthesis (step 2), nucleic acid amplification (PCR), and synthesis of 2nd cDNA into which known terminal sequences necessary for sequencing are introduced. The steps are divided into (step 3) (step 4) and PCR amplification (step 5).

  After washing the cells with 500 μL of 1 × PBS buffer so as not to damage the cells, 1000 cells suspended in 10 μL of 1 × PBS buffer cooled to 4 ° C. were introduced from the upper inlet 307. Aspirate from top outlet 308 to fill with this solution. By doing so, the two-dimensional array chip 315 is filled with a PBS buffer containing cells. Next, a negative pressure of 0.95 atm is applied to the lower outlet 310 so that the solution flows through the cell trapping portion 203 toward the lower channel 309, and the solution is sucked. The cells move along the flow of the solution, reach the cell capturing unit 203, and since the opening diameter of the cell capturing unit 203 is smaller than the diameter of the cells, the cells are captured here. Since the trapped cells act as plugs for the solution flow, the flow moves to the cell trap 203 that has not yet trapped the cells. Therefore, the remaining cells move to the part where the cells are not yet captured and are captured.

  When only a sufficient number of cells have been captured, excess cells that have not been captured and PBS buffer are drained from the upper outlet 308. Next, a lysis buffer (for example, a surface active agent such as Tween 20) is flowed from the upper inlet 307 toward the upper outlet 308, and immediately after the two-dimensional array chip 315 is filled with the buffer, negative pressure is immediately applied to the lower outlet 310. Apply and suck. Thereafter, all the solutions are passed through the nucleic acid capturing unit 202 of the two-dimensional array chip 315 by the same method. At this time, the bead outflow prevention membrane is a flow path composed of a porous material having a diameter of 0.8 μm, and since the pressure loss is large, the lysis buffer passes through the cell trapping part 203 toward the lower flow path 309 for about 5 minutes. It is easy to keep it flowing slowly.

  The trapped cells 300 are crushed by the lysis buffer, and the mRNA 806 goes out of the cells, but the flow of the cell solution around the cell trapping part 203 continues to be sucked into the holes constituting the cell trapping part 203. Therefore, the mRNA 806 reaches the nucleic acid capturing unit 202 through the cell capturing unit 203 without diffusing to the periphery. In this way, by introducing the lysis buffer, disruption of cells and capture with the first DNA probe 801 immobilized on the beads of the nucleic acid capture unit 202 of mRNA 806 are simultaneously performed. This is shown in step 1 of FIG.

  Here, the position information on the two-dimensional array chip 315 where the cells are trapped, that is, the position coordinates of the cell trapping sections 203 arranged in a grid as shown in FIG. Therefore, on the bead surface of the nucleic acid capture unit 202, a first DNA probe 801 having a cell recognition sequence 802 having a different sequence for each cell capture unit 203 is fixed. In FIG. 8, the diagonal line at the left end of each step diagram indicates the fixed wall surface, here the bead surface. This first DNA probe 801 has a poly T sequence in the 3 ′ end region, and captures mRNA 806 by hybridizing with the poly A sequence at the 3 ′ end of mRNA. In addition, a common primer (804, Reverse) for PCR amplification is provided on the 5 ′ end side.

  This first DNA probe 801 has a 30 base PCR amplification common primer (804, Reverse) from the 5 ′ end, a 7 base cell recognition sequence (802), and an 18 base oligo (dT) sequence + 2 bases. Arrange in order of VN sequence. In this example, a poly-T sequence was used as a part of the complementary DNA probe 801 to analyze mRNA. However, in order to perform microRNA or genome analysis, a random sequence is complementary to the sequence to be analyzed instead of the poly-T sequence. A part of the arrangement may be used.

  Next, as shown in Step 2 of FIG. 8, 1st cDNA 807 is synthesized using mRNA 806 captured by first DNA probe 801 as a template. 10 mM Tris Buffer with 0.1% Tween20 (pH = 8.0) 58.5 μL, 10 mM dNTP 4 μL, 5xRT Buffer (SuperScript III, Invitrogen) 225 μL, 0.1 M DTT 4 μL, RNaseOUT (Invitrogen) 4 μL, and Superscript 3 μL of III (reverse transcriptase, Invitrogen) is mixed and introduced from the upper inlet 307 as in the previous step. While the above solution was filled in the void portion of the beads filled with the solution containing the reverse transcriptase and the synthetic substrate, the temperature was raised slowly to 50 ° C. while flowing very slowly from the reaction chamber 302 to the lower flow path 309. Complementary strand synthesis reaction (1st cDNA synthesis reaction) was performed for about 5 minutes. As a result, cDNA immobilized on the surface of a plurality of beads for each cell was obtained as a library. This is a so-called 1-cell cDNA library array, which is fundamentally different from the averaged cDNA library obtained from many cells.

  After synthesizing the 1st cDNA strand 807, the entire device was kept at 85 ° C. for 1.5 minutes to inactivate the reverse transcriptase. Furthermore, after cooling to 4 ° C., 0.2 mL of 10 mM Tris Buffer (pH = 8.0) containing RNase and 0.1% Tween 20 was injected from the upper inlet 307 and sucked from the upper outlet 308 to fill the reaction chamber 302 with the solution. Then, the process of discharging from the lower outlet 310 and removing the buffer in the reaction chamber 302 from the upper outlet 308 was repeated five times to decompose the mRNA, and the residue and decomposed product in the nucleic acid capturing part were removed and washed. Further, it was washed 5 times in the same manner with a solution containing an alkali denaturant and a washing solution. Through the process so far, a cDNA library array corresponding to all the cells is constructed for each captured cell as shown in step 2 of FIG.

  Next, Ex Taq Hot start version (TaKaRa Bio) with 69 μL of sterilized water, 10 μL of 10 x Ex Taq Buffer (TaKaRa Bio), 2.5 μm dNTP Mix 100 μL, and 10 μM each of the PCR amplification consensus sequence (Reverse) 809 was added. 1 μL was mixed, and this mixed reagent was introduced from the upper inlet 307 to the nucleic acid capturing unit 202 in the same manner as in the previous step. A method for individually introducing the second DNA probe with the chip identification tag 810 will be described later. Subsequently, the secondary structure of the nucleic acid was solved at 95 ° C. for 3 minutes, and then the primer gene-specific sequence 811 was annealed at 44 ° C. for 2 minutes using the 1st cDNA strand as a template. Step 3 in FIG. 8 shows how the second DNA probe 808 is hybridized to st cDNA. Further, the complementary strand extension reaction was carried out by raising the temperature to 72 ° C. for 6 minutes to synthesize the 2nd cDNA strand 812 (step 4 in FIG. 8).

  The second DNA probe 808 is introduced into the reaction chamber 302 as follows. First, mineral oil is introduced from the upper inlet 307 and discharged from the upper outlet 308. Next, a buffer solution containing salt is allowed to flow from the lower channel 309 toward the individual inlet 311, and excess mineral oil in the reaction chamber is discharged from the individual inlet 311. By doing in this way, the area | region of the two-dimensional array chip | tip 315 of the reaction chamber 302 is isolate | separated with mineral oil. Such separation occurs because the inner wall of the reaction chamber 302 is hydrophilic while the surface treatment is performed so that the region 316 between the reaction chambers is hydrophobic. It is also important to maintain high reaction efficiency that the 1st cDNA is firmly fixed to the beads (for example, by biotin-avidin binding). After the separation of the reaction chamber 302 is completed, a buffer solution containing a second DNA probe having a different chip identification sequence is introduced from the individual inlet 311 and discharged from the lower outlet 310 through the lower channel 309. As a result, the vicinity of the nucleic acid capture unit 203 is filled with the second DNA probe that is different for each reaction chamber 302, and this probe hybridizes to the 1st cDNA. After the synthesis of the 2nd cDNA is completed, a large amount of buffer solution is poured from the upper inlet 307 toward the upper outlet 308, and the mineral oil in the region 316 is washed away. Some mineral oil may remain in the region 316 as long as the flow paths are connected.

  The last step is PCR amplification using common primers as shown in Step 5 and Step 6 of FIG. Sterile water 49 μL, 10 x High Fidelity PCR Buffer (Invitrogen) 10 μL, 2.5 mM dNTP mix 10 μL, 50 mM MgSO4 4 μL, 10 μM PCR amplification common primer (Forward) 10 μL, 10 μM PCR amplification common sequence primer (Reverse) 10 μL, and Platinum Taq Polymerase High Fidelity (Invitrogen) 1.5 μL was mixed to prepare a reagent, which was then introduced from the upper inlet 307 as in the previous step. Subsequently, keep the entire device at 94 ° C for 30 seconds, repeat 40 cycles of 3 steps of 94 ° C for 30 seconds → 55 ° C for 30 seconds → 68 ° C for 30 seconds, finally hold at 68 ° C for 3 minutes, then increase to 4 ° C The PCR amplification process was performed after cooling. This reaction is a common reaction, and by performing PCR amplification under the same conditions for all the chips, it is possible to make the amplification efficiency uniform among the chips. PCR Purification Kit (QIAGEN) is used to collect the PCR amplification product solution accumulated in the solution and remove residual reagents such as free PCR amplification common sequence primers (Forward / Reverse) and enzymes contained in this solution. ).

  The obtained PCR product 815 is a sequence that can be sequenced, and is called a sequencing library. Even if an amplification bias occurs between genes or molecules in the above-mentioned process, it is possible to correct the amplification bias using molecular recognition tags after acquiring sequencing data, so that highly accurate quantitative data can be obtained. I can do it. By analyzing the sequence of this sequencing library, a gene expression level can be obtained for each cell identification sequence and chip identification sequence. That is, it is possible to simultaneously analyze the number of cells equal to or less than the product of the type of the cell identification sequence and the type of the chip identification sequence simultaneously introduced into the device. As a result, it is possible to analyze the number of cells significantly larger than the number of cell identification sequences introduced in advance into the two-dimensional array chip.

  Note that the present inventors have already filed an international patent application (PCT / JP2014 / 073753) for a cell analysis method that enables simultaneous gene analysis of a single cell and comprehensive gene analysis of a cell population containing the cell. )It is carried out. The contents described in the specification, claims, and drawings of the application are incorporated herein by reference as they are.

(Example 1-3) Comparison of solution suction speed Solution suction between the device according to the present invention shown in FIG. 2 and a device according to the prior art that does not use capillary action due to the three-dimensional porous body as shown in FIG. The speed was compared. In either case, a syringe pump was connected to the lower outlet, and an initial negative pressure was applied at the same pressure. In the device according to the present invention, a 3 μm pore SPG film having a size of 1.3 × 1.3 × 0.7 mm was used for each two-dimensional array chip as a three-dimensional porous body. The comparison results of the suction speed are shown in FIG. It was found that there was a difference in suction force of about one order of magnitude between the two.

(Example 2)
FIG. 9 is a diagram showing an outline of the configuration of a device according to another embodiment of the present invention, (a) is a top view, (b) is a cross-sectional view in the 9A-9A ′ cross section, (c) is (b) FIG. In the device of the present embodiment, the method for discharging the aqueous solution absorbed by the liquid holding unit 211 is different from that of the first embodiment. Hereinafter, differences from the device of the first embodiment will be described.

  In the device of this embodiment, the same number of intake ports 319 as the number of two-dimensional array chips 315 are installed so that the air flow from the intake ports 319 to the lower outlet 310 is parallel. That is, in the device of Example 1, the solution holding unit 211 is connected in series by the flow path, whereas in the device of this example, the solution holding unit 211 is connected in parallel by the flow path. The same air valve 318 and pressure adjustment filter 320 installed in the intake port 319 as those in Example 1 were used. Thus, by providing the intake ports 319 individually, absorption by the solution holding unit 211 can be controlled for each two-dimensional array chip 315. For the solution holding unit 211, an aggregate of glass beads having a diameter of 10 μm was used instead of the SPG film used in Example 1.

  FIG. 10 is a diagram showing an example of the configuration of an apparatus that includes the device shown in this embodiment and can automatically execute sample preparation. The control unit 1009 includes a cell introduction control device 1011 that controls the introduction of cells into the device, a valve control device 1020 that controls the air valve 318 of the intake port 319, a lysis buffer for disrupting cells, and cDNA synthesis and PCR amplification. Reagent introduction control device 1012 for controlling introduction of enzyme reagent, second DNA probe, mineral oil for separating reaction chamber, unnecessary reagent, cells, mineral oil for separating reaction chamber, etc. Upper reagent discharge device 1014 for controlling discharge, and lower reagent discharge device 1015 for discharging cells and introducing various enzyme reagents, DNA probes, substrates, etc. and discharging prepared nucleic acid amplification products Is properly controlled. The thermometer provided in the device is connected to a temperature control device 1016 to control the reaction temperature. In addition, the device is connected to a stage controller for enabling the XYZ position of the observation field of the device to be changed for microscopic observation.

  More specifically, the cell introduction control device 1011 and the reagent introduction control device 1012 store cells and various reagents (enzyme reagent, substrate, DNA probe, primer) at an appropriate temperature, and at the upper timing of the device at an appropriate timing. In order to introduce into 307 or individual inlet 311, it is configured such that the piping inside each introduction control device can be switched using a switching valve. Further, the upper reagent discharging device 1014 and the lower reagent discharging device 1015 have a syringe pump or the like inside, and discharge them by sucking the reagent or the cell solution. Of course, the waste liquid accumulated in the syringe can be discharged into the waste liquid bottle. The temperature control device 1016 has the ability to control the temperature of the reaction chamber between 4 ° C. and 98 ° C., and is composed of a Peltier element 1017 and its control device.

(Example 3)
FIG. 11 is a diagram showing an outline of the configuration of a device according to another embodiment of the present invention, (a) is a top view, (b) is a cross-sectional view in the 11A-11A ′ cross section, (c) is (b) FIG. In the device of this embodiment, the configuration of the lower flow path 1109 is different. That is, the application of the negative pressure for discharging the aqueous solution absorbed by the solution holding unit 211 is not performed in the direction parallel to the two-dimensional array chip 315 as shown in FIG. The lower flow path 1109 is configured so that it can be performed in the vertical direction. By adopting such a flow path configuration, the air flow does not bypass the solution holding unit 211, and the solution absorbed by the solution holding unit 211 can be discharged more efficiently. In this configuration, a hydrophilic porous membrane may be further disposed adjacent to the solution holding part 211 and the lower flow path 1109. By doing so, the discharge of the solution from the solution holding unit 211 to the lower channel 1109 proceeds more smoothly.

  In the embodiment shown in FIG. 11, one intake port 319 is installed for a plurality of two-dimensional array chips 315. However, as with the embodiment shown in the second embodiment, one two-dimensional array chip 315 is provided. One intake port 319 may be installed. This embodiment is shown in FIG. In this case, as in Example 2, the suction of the solution can be controlled for each two-dimensional array chip.

(Example 4)
In Examples 1 to 3, a cell solution and a reaction reagent are introduced from the upper inlet 307, and the solution is filled on the two-dimensional array chip by sucking from the upper outlet 308, and then negative pressure is applied to the lower outlet 310. In this example, the cell solution and the reagent are individually introduced into the introduction well 1330, and the reagent is introduced into and discharged from the nucleic acid capturing unit. did. The structure of the device is shown in FIG. By adopting such a flow path configuration, it is possible to eliminate the possibility of problems such as cell adsorption in the middle from the upper inlet to the two-dimensional array chip.

  All publications, patents and patent applications cited herein are incorporated herein by reference in their entirety.

1 ... cell, 2 ... porous membrane, 3 ... cell trapping part, 4 ... upper region, 5 ... lower region, 6 ... inlet, 7 ... upper outlet, 8 ... lower outlet, 9 ... cell, 201 ... cell, 202 ... Nucleic acid capture unit, 203 ... cell capture unit, 204 ... upper region, 206 ... upper inlet, 207 ... upper outlet, 208 ... lower outlet, 211 ... solution holding unit (three-dimensional porous body), 212 ... pressure adjusting member, 213 Inlet port, 214 ... Air flow, 300 ... Cell, 301 ... Device, 302 ... Reaction chamber, 305 ... Common flow path, 307 ... Upper inlet, 308 ... Upper outlet, 309 ... Lower flow path, 310 ... Lower outlet, 311 ... Individual inlet, 315 ... Two-dimensional array chip, 316 ... Area between reaction chambers, 318 ... Air valve, 319 ... Intake port, 320 ... Pressure regulating filter, 801 ... First DNA probe, 802 ... Cell recognition sequence, 804 ... Common primer, 806 ... mRNA, 807 ... 1st cDNA, 808 ... Second DNA Lobe, 809 ... Common sequence for PCR amplification (Reverse), 810 ... Chip identification tag, 811 ... Gene specific probe, 812 ... 2nd cDNA, 813 ... Common primer, 814 ... Common sequence for PCR amplification (Forward), 815 ... PCR Product, 901 ... Device, 1001 ... Device, 1009 ... Control unit, 1011 ... Cell introduction control device, 1012 ... Reagent introduction control device, 1014 ... Upper reagent discharge device, 1015 ... Lower reagent discharge device, 1016 ... Temperature control device, 1017 ... Peltier element, 1020 ... Valve control device, 1101 ... Device, 1109 ... Lower flow path, 1201 ... Device, 1301 ... Device, 1330 ... Introduction well

Claims (11)

A two-dimensional array having a plurality of cell capture units capable of capturing cells one by one and a nucleic acid capture unit that exists corresponding to each cell capture unit and captures nucleic acid extracted from the cells captured by the cell capture unit A device for single cell analysis with a chip,
A solution holding unit provided adjacent to the nucleic acid capturing unit of the two-dimensional array chip; and the solution holding unit absorbs a solution staying in the nucleic acid capturing unit by capillary action and applies a negative pressure. It has a three-dimensional porous body that can discharge the solution absorbed by
The device is configured such that the solution holding unit is adjacent to the flow channel, and can apply a negative pressure to the solution holding unit, the nucleic acid capturing unit, and the cell capturing unit by applying a negative pressure to one end of the flow channel. .   The flow path communicates with an intake port opened to the outside of the device, and external air is taken in from the intake port by applying a negative pressure to one end of the flow path, and the air flow passes through the solution holding unit. The device according to claim 1, wherein the solution is discharged from the solution holding unit.   3. The device according to claim 2, further comprising a plurality of two-dimensional array chips and a solution holding unit corresponding to each two-dimensional array chip, wherein the flow path connects the plurality of solution holding units in series.   A plurality of two-dimensional array chips and a solution holding unit corresponding to each two-dimensional array chip are provided, the flow path connects a plurality of solution holding units in parallel, and the intake port is provided for each individual solution holding unit. 3. The device according to claim 2, wherein a plurality of devices are provided.   The device according to any one of claims 1 to 4, wherein the absorption time of the liquid droplets when 1 μL of pure water is dropped on the surface of the three-dimensional porous body is within 10 seconds.   The device according to any one of claims 1 to 4, wherein the three-dimensional porous body is a porous glass material, a glass fiber aggregate, or a glass bead aggregate.   The nucleic acid capture unit has a nucleic acid probe for capturing a nucleic acid, and the nucleic acid probe has a nucleic acid capture sequence that hybridizes with a nucleic acid extracted from a cell, and a different cell recognition sequence corresponding to each cell capture unit. The device according to any one of claims 1 to 4.   8. The device according to claim 7, wherein the nucleic acid capturing unit has a structure filled with beads to which a nucleic acid probe is immobilized.   3. A single cell analysis method using the device according to claim 1, wherein the two-dimensional array chip is filled with a cell solution, and negative pressure is applied to one end of a channel adjacent to the solution holding unit. The method includes the steps of applying a negative pressure to the cell trapping unit by applying a solution to absorb the cell solution in the solution holding unit and adsorbing a single cell to the cell trapping unit.   The method further comprises a step of crushing a single cell adsorbed on the cell trapping part in a state where a negative pressure is applied to the cell trapping part, and causing the nucleic acid trapping part to capture a nucleic acid extracted from the cell. 9. The analysis method according to 9.   The second nucleic acid probe having a sequence that hybridizes with the nucleic acid captured in the nucleic acid capturing part, and an enzyme and substrate for synthesizing a complementary strand using the captured nucleic acid as a template are supplied to the nucleic acid capturing part to obtain a complementary strand. 11. The analysis method according to claim 10, further comprising a step of performing synthesis.

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