Amplification of Escherichia coli in a Continuous-Flow-PCR Microfluidic Chip and Its Detection with a Capillary Electrophoresis System

摘要

This protocol describes how to build a continuous-flow-polymerase chain system based on a microfluidic chip and how to build a capillary electrophoresis system in the lab. It presents a simple method for the analysis of nucleic acids in the lab.

摘要

Polymerase chain reaction (PCR) is a traditional method employed for the amplification of a target gene that has played an important role in biomolecular diagnostics. However, traditional PCR is very time-consuming because of the low-temperature variation efficiency. This work proposes a continuous-flow-PCR (CF-PCR) system based on a microfluidic chip. The amplification time can be greatly reduced by running the PCR solution into a microchannel placed on heaters set at different temperatures. Moreover, as capillary electrophoresis (CE) is an ideal way to differentiate positive and false-positive PCR products, a CE system was built to achieve efficient separation of the DNA fragments. This paper describes the process of amplification of Escherichia coli (E. coli) by the CF-PCR system built in-house and the detection of the PCR products by CE. The results demonstrate that the target gene of E. coli was successfully amplified within 10 min, indicating that these two systems can be used for the rapid amplification and detection of nucleic acids.

引言

Polymerase chain reaction (PCR) is a molecular biology technique used to amplify specific DNA fragments, thereby amplifying trace amounts of DNA hundreds of millions of times. It has been widely used in clinical diagnosis, medical research, food safety, forensic identification, and other fields. The PCR process mainly consists of three steps: denaturation at 90-95 °C, annealing at 50-60 °C, and extension at 72-77 °C. Thermal cycling is an important part of the PCR process; however, the traditional PCR thermal cycler is not only bulky but also inefficient, requiring approximately 40 min to complete 25 cycles. To overcome these limitations, a continuous-flow PCR (CF-PCR) system was built in-house, based on a microfluidic chip. CF-PCR can greatly save time by driving the PCR solution into microchannels placed on heaters at different temperatures^1,2,3,4,5.

As capillary electrophoresis (CE) has many advantages, such as high resolution, high speed, and excellent reproducibility^{6,7,8,9,10,11}, it has become a popular tool in the lab for the analysis of nucleic acids and proteins. However, most labs, especially labs in the developing world, cannot afford this technology because of the high price of the CE instrument. Herein, we have outlined protocols for how to fabricate the CF-PCR microfluidic chip and how to build a versatile CE system in the lab. We also demonstrate the process of amplification of E. coli by this CF-PCR system and the detection of the PCR products by the CE system. By following the procedures described in this protocol, users should be able to fabricate microfluidic chips, prepare PCR solutions, build a CF-PCR system for nucleic acid amplification, and set up a simple CE system, even with limited resources, to separate DNA fragments.

方案

NOTE: See the Table of Materials for details related to all materials, reagents, and equipment used in this protocol.

1. Fabrication of CF-PCR microfluidic chip

1. Heat the silicon wafer at 200 °C for 25 min to remove the moisture.
2. Dispense 1 mL of SU-8-2075 photoresist per inch of the wafer. Spin it on the silicon wafer using a spin coater at 500 rpm for 5-10 s with an acceleration of 100 rpm/s, and then at 2,000 rpm for 30 s with an acceleration of 500 rpm/s.
3. Soft bake the silicon wafer at 65 °C for 3 min, then at 95 °C for 15 min.
4. Set 150 - 215 mJ/cm² as the exposure energy for the photolithography machine, and engrave the designed pattern onto the photoresist with a photolithography mask. Place the silicon wafer and the mask ready for exposure.
5. Post exposure, bake the silicon wafer at 65 °C for 2 min, and then at 95 °C for 7 min.
6. Immerse the silicon wafer in developer solution to remove excess photoresist and take it out when the microchannels can be seen (Figure 1). Use isopropanol to rinse off the residual developer solution.
7. Mix the polydimethylsiloxane (PDMS) prepolymer and curing agent at a ratio of 10:1. Pour the mixed PDMS solution into the replica mold and solidify it at 80 °C for 60 min.
8. Bond the PDMS microfluidic chip on a slide after activation using a plasma cleaner, and solidify them at 80 °C for 30 min as soon as possible (Figure 2).
   NOTE: The outer dimensions of the chip are 80.0 mm × 30.0 mm × 0.4 mm. There are 40 serpentine channels (100 µm × 1.46 mm × 100 µm, width × length × depth) in the microfluidic chip.

2. Preparation of the PCR solution

1. Thaw the reagents completely before configuration. Use a vortex mixer and centrifuge to ensure the reagents are well mixed.
2. Prepare a centrifuge tube, adding the following components in this order: 33.75 µL of water, 1.0 µL of DNA template, 0.5 µL of primer, 5.0 µL of buffer, 4.0 µL of dNTP mixture, 1.5 µL of Tween 20, 3.5 µL of PVP, and finally 0.25 µL of DNA polymerase.
   NOTE: Here, the DNA template used is E. coli. The primers for E. coli and the components of the PCR solution are listed in Table 1 and Table 2, respectively.
3. Mix the solution by vortexing.

3. Construction of the CF-PCR system

1. Prepare two positive temperature coefficient (PTC) ceramic heaters, two solid-state relays, two PID temperature controllers, two temperature sensors, and a power cord.
   NOTE: The size of the PTC ceramic heaters depends on the size of the microfluidic chip; the length should be greater than the length of the chip-the length-width-height of the PTC ceramic heaters used here is 10 cm x 2 cm x 0.4 cm.
2. Connect the heater to the solid-state relay.
3. Connect the solid-state relay to the PID temperature controller.
4. Attach the temperature sensor probe to the bottom of the two heaters and connect the terminal to the PID temperature controller.
5. Connect two solid-state relays in series and connect the power cord.
6. 3D print a slot for the two heaters and keep the heaters on the same plane (see Supplemental File 1 for STL files required for 3D printing).
   NOTE: Leave a 12 mm air gap between the two heaters.
7. Place the microfluidic chip on the two heaters.
8. Prepare a syringe pump and a syringe, fix the syringe on the syringe pump, connect a silicone tubing (0.8 mm inner diameter [ID]) with a syringe, and connect a steel needle (0.7 mm ID) to the top of the silicone tubing (Figure 3).
9. Insert the steel needle into the inlet of the microfluidic chip.
10. Place a pipette tip at the outlet of the chip to collect the PCR products.

4. Construction of the CE system

1. Use a high-voltage power supply to generate a pulsed-field electric field; note the positive and negative electrodes.
2. Use a mercury lamp as the light source and filter the excitation wavelength from the mercury lamp through a filter.
3. Place the capillary on the microscope stage.
4. Collect the fluorescence emission with the objective, and then detect it using an R928 photomultiplier tube (PMT). Observe the microscope and the capillary. Turn on the light under dark room conditions; excitation light is collected by the objective.
5. Use the self-developed LABVIEW software to control the power supply and complete the data acquisition (described in steps 6.3-6.6). See https://github.com/starliyan/labview/blob/main/CZE20170723.vi.
   ​NOTE: All experiments were performed in a dark room, and the schematic of the CE system is shown in Figure 4.

5. Run the PCR solution

1. Preset the temperature of the heaters of the CF-PCR system at 65 °C and 95 °C.
2. Place the microfluidic chip on the two heating blocks.
3. Insert the tip of the silicone tube into a centrifuge tube containing 50 µL of the PCR solution (from step 2.3). Pull the syringe plunger to slowly withdraw the solution. Fix the syringe on a syringe pump. Insert the steel needle into the inlet of the microfluidic chip.
4. Set the flow rate of the pump to 10 µL/min and press the start button to push the solution in the microchannel at the inlet of the microchip.
5. Collect the PCR products at the outlet of the microfluidic chip.
   ​NOTE: Rinse the channel with ultrapure water before and after the PCR to remove impurities.

6. Detection of the PCR products by this CE system built in-house

1. Prepare a capillary with an 8 cm total length and a 6 cm effective length.
2. Prepare the separation buffer by mixing 100 µL of 1% hydroxyethylcellulose (HEC, w/v), 2 µL of 100x SYBR Green I, and 98 µL of ultrapure water to obtain 0.5% HEC (w/v) containing 1x SYBR Green I.
3. Fill the capillary with the prepared separation buffer using a vacuum pump.
4. Input the injection voltage (800 V) and the injection time (2.0 s) on the software interface, click the start button, and wait for the PCR products to be electrodynamically introduced into the capillary at 100 V/cm (2.0 s).
   NOTE: In this step, the PCR products are placed on the negative electrode and the buffer is placed on the positive electrode.
5. Input the DC voltage (800 V) on the software interface, click the start button, and run the electrophoresis at 100 V/cm of electric field strength.
   NOTE: In this step, both the positive and negative electrodes are placed with buffer.
6. Click the stop button after all DNA fragments are separated in the capillary.
7. Flush the capillary with sterilized water for 1 min after each run.

结果

Figure 5 represents the electropherogram of the PCR products and the DNA markers. Trace (Figure 5A) is the CE result of the CF-PCR amplified product, trace (Figure 5B) is the CE result of the product amplified by thermal cycling, and trace (Figure 5C) is the CE result of the 100 bp DNA ladder. We first amplified the target gene of E. coli in the CF-PCR system; the PCR solution took ~10 min, 30 ...

讨论

Both PCR and CE are two popular biotechnologies in the analysis of nucleic acids. This paper describes the amplification of E. coli and the detection of the PCR products using the CF-PCR and CE systems, both built in-house. The target gene of E. coli was successfully amplified within 10 min because of the high heat transfer rates. The DNA fragments smaller than 1,500 bp were separated within 8 min (Figure 5). The great advantage of these two techniques is that it can greatl...

材料

本文使用的材料清单

姓名	公司	目录编号	评论
100 bp DNA 分子量标准	Takara Bio Inc.	3422A
10x Fast 缓冲液 I	Takara Bio Inc.	RR070A
10x TBE	北京阳光生物科技科技有限公司	T1051
显影液	Alfa Aesar， USA	L15459
dNTP 混合物 （2.5 μM）	Takara Bio Inc.	RR070A
EC-F	Sangon Biotech，中国
EC-R	Sangon Biotech，中国
HEC，1300K	Sigma-Aldrich，美国	9004-62-0
异丙醇	阿拉丁，中国上海	67-63-0
显微镜	日本奥林巴斯	BX51
光刻	SUSS MicroTec，德国	MJB4
光电倍增管	日本滨松光子学公司	R928
光刻胶	MicroChem，美国	SU-8 2075
PID 温度控制器	中国上海	XH-W2023
等离子清洗机	Harrick Plasma	PDC-32G-2
聚乙烯吡咯烷酮 （PVP）	阿拉丁，上海，中国	P110608
泵	Harvard Apparatus	PHD2000
硅胶管	美国 BIO-RAD
固态继电器	KZLTD，中国	KS1-25LA
SpeedSTAR HS DNA 聚合酶	Takara Bio Inc. 公司	RR070A
钢针	中新齐横，苏州，中国
SYBR GREEN	Solarbio，中国北京	SY1020
温度传感器	EasyShining Technology，中国成都	TCM-M207
模板（大肠杆菌）	Takara Bio Inc.	AK601
Tween 20	Aladdin， 上海， 中国	T104863
电压电源	美国纽约州梅迪纳	TREK 型号 610E