A Droplet-Based Microfluidic Approach and Microsphere-PCR Amplification for Single-Stranded DNA Amplicons

摘要

This work provides a method for the fabrication of droplet-based microfluidic platforms and the application of polyacrylamide microspheres for microsphere-PCR amplification. The microsphere-PCR method makes it possible to obtain single-stranded DNA amplicons without separating double-stranded DNA.

摘要

Droplet-based microfluidics enable the reliable production of homogeneous microspheres in the microfluidic channel, providing controlled size and morphology of the obtained microsphere. A microsphere copolymerized with an acrydite-DNA probe was successfully fabricated. Different methods such as asymmetric PCR, exonuclease digestion, and isolation on streptavidin-coated magnetic beads can be used to synthesize single-stranded DNA (ssDNA). However, these methods cannot efficiently use large amounts of highly purified ssDNA. Here, we describe a microsphere-PCR protocol detailing how ssDNA can be efficiently amplified and separated from dsDNA simply by pipetting from a PCR reaction tube. The amplification of ssDNA can be applied as potential reagents for the DNA microarray and DNA-SELEX (Systematic evolution of ligands by exponential enrichment) processes.

引言

Single-stranded DNA (ssDNA) has been extensively considered as a molecular recognition element (MRE) due to its intrinsic properties for DNA-DNA hybridization^1,2. The development of ssDNA synthetic systems can lead to biological applications such as DNA microarrays³, oligotherapeutics, diagnostics, and integrated molecular sensing based on complementary interactions^4,5.

To date, micrometer-scale polymer particles have been successfully demonstrated using microfluidic devices. Several microfluidic techniques have been proven to be powerful for producing highly homogenous microspheres on continuous flow in the microchannel environment^6,7.

In the study of Lee et al.⁸, a droplet-based microfluidic platform for the microfluidic synthesis of copolymerizable oligo-microsphere and ssDNA amplification was reported. The microfluidic platform consists of two PDMS (polydimethylsiloxane) layers: an upper part with a microfluidic channel network for generating microsphere and a bottom flat part. These consist of three kinds of PDMS fluidic channels: 1) a flow focusing channel for droplet generation, 2) a serpentine channel for mixing two solutions, and 3) a sequential polymerization channel for microsphere solidification. Once two immiscible flows are introduced into a single PDMS fluidic channel, the flows can be forced through the narrow orifice structure. The flow behaviors such as channel geometry, flow-rate, and viscosity affect the size and morphology of the microsphere. Therefore, the main liquid stream can be divided into microscale monospheres^9,10.

Here, a detailed microsphere-PCR protocol is provided for the amplification of ssDNA. First, a droplet-based microfluidic device design process is described. Then, the way in which polyacrylamide microspheres can be functionalized with random DNA template in a complementary manner is explained. Finally, a microsphere-PCR protocol for amplifying ssDNA is shown.

方案

1. Fabrication of a PDMS Microfluidic Platform

1. Prepare 20 mL of liquid PDMS prepolymer by mixing base polymer and catalyst in a volume ratio of 10:1. Pour 10 mL of the liquid PDMS onto a prepared SU-8 mold on a silicon wafer for the upper part of the microfluidic network. For the bottom flat part, pour the same volume of liquid PDMS on the silicon wafer without a mold structure.
   Note: The microfluidic network is designed in a CAD program and then converted into a photomask in order to fabricate a master using the typical photolithography process (See Supplemental Figures). This master is comprised of the negative photoresist SU-8 mold on the silicon wafer¹¹.
2. Place two silicon wafers coated with liquid PDMS prepolymer on the hot plate and cure at 75 °C for 30 min.
   1. Manually peel off the cured PDMS layer from the SU-8 mold. Align a 1.5 mm diameter round hole punching tool to the oil port on the replicated microfluidic network for interfacing micron-scale flow channels with the macro fluid samples. Punch out the through-hole manually.
   2. Repeat this punching process three times for the formation of the two solutions and the outlet port.
3. Perform hydrophilic surface treatment on both the upper and bottom PDMS layers using a hand-held corona treater¹² for several seconds per sample.
   1. Stack two plasma-treated PDMS layers and heat at 90 °C for 30 minutes using a hot plate for the PDMS-to-PDMS bonding process. Supply the pressurized water using the syringe pump into three inlet ports for the structural bonding and leakage testing of the fabricated device.

2. Production of Polyacrylamide Oligo-Microspheres

1. Prepare bead-mixture detailed in Table 1.
2. Vortex and briefly centrifuge the standard ssDNA acrydite labeled probe (Ap, 100 μM) and acrylamide:bis (19:1) stock solution.
3. Prepare solution I by mixing 25 μL of 40% acrylamide bis solution, 10 μL of ssDNA (acrydite probe), 10 μL of 5x TBE buffer (1.1 M Tris; 900 mM borate; 25 mM EDTA), and 5 μL of water. Prepare solution II with 50 μL of 20% ammonium persulfate.
4. Prepare two syringes individually filled with solution I and solution II, and mount them onto the pump to introduce solution flows into the microfluidic platform. Prepare mineral oil mixed with 0.4% TEMED for surface solidification of the microsphere.
   Note: TEMED is well-known as a free radical stabilizer. Free radicals can accelerate the rate of polymer formation with ammonium persulfate (APS) in order to catalyze acrylamide polymerization.
5. Fill a glass bottle with 4 mL of the mineral oil to generate a continuous flow.
6. Insert two tubes to two ports in the cap of the glass bottle as a microfluidic reservoir: the pneumatic port for applying the compressed air into the glass bottle from the air compressor and the fluid port for supplying the pressurized oil to the micro channel network from the glass bottle. Connect tubes between the glass bottle and the oil port in the microfluidic device.
   1. Connect the tubes to the two solution ports in the microfluidic device in order to supply the two solutions from the syringe pumps. Insert tubes to the outlet port in order to transfer the generated microsphere into the beaker.
7. Set the flow rate of the syringe pump to 0.4 - 0.7 mL/h. Adjust compressed air pressure of the compressor using a regulator (82 - 116 kPa). Set the rotational speed (500 rpm) of the magnetic stirrer bar in the glass beaker on a hot plate. Operate the syringe pump and supply the compressed air generated by an external compressor into the glass bottle using the ON/OFF control of an electromagnetic valve¹³.
8. Observe the formation of microspheres in the flow-focusing geometry and solidification of generated microspheres in the glass beaker with a digital microscope.
   Note: The size and production speed of the microsphere depend on the flowrate of solutions and the pressure applied for the mineral oil flow (Table 2).

3. Performing Polyacrylamide Oligo-Microspheres Counts

1. For hemocytometer quantification, take a small amount (approximately 100 μL) of aqueous solution of polyacrylamide oligo-microspheres and place on the glass hemocytometer, and gently fill the microsphere suspension up the well of the counting chamber.
   Note: For further details, see http://www.abcam.com/protocols/counting-cells-using-a-haemocytometer.
2. Use a microscope and hand tally counter to count microspheres in one set of 16 squares. Then, move the hemocytometer to the next set of the chamber and carry on counting until all four sets of 16 corners are counted.
3. Determine the average microsphere count and calculate the number of microspheres in the original bead suspension.
4. Transfer 100 μL of microspheres to a 1.5 mL microcentrifuge tube. Remove the supernatant through gentle centrifuging (400 x g) and pipetting.

4. Performing DNA Hybridization on the Surface of Polyacrylamide Oligomicrosphere

Note: An identical DNA probe with a 5’-NH₂-group instead of 5’-acrytide modification is added into solution I and tested for Ap-containing microspheres in parallel. DNA hybridization results are shown in Figure 2. The Cy3-labeled complementary oligonucleotide probes (cAp) solution should be placed in a dark room.

1. Resuspend Cy3-cAp using 100 μL of 1xTE buffer (TE buffer: 10 mM Tris and 1μM EDTA, pH 8.0) in order to achieve a final concentration of 100 μM. For example, resuspend 1 pmol of cAp in 100 mL of TE buffer and transfer to a microcentrifuge tube covered with aluminum foil.
   Note: For strand sequences, see Table 3.
2. Add 100 μM of Cy3-cAp to a sterile 1.5 mL microcentrifuge tube containing Ap-copolymerized microspheres.
3. Tap the tube a few times to mix and incubate at room temperature in the dark for 1 h.
4. Discard the supernatant and remove residual buffer through pipetting.
5. Rinse three times with 500 μL of TE buffer.
6. Resuspend microspheres by gently tapping the microcentrifuge tube. Then, repeat step 4.4.
7. Place microspheres on the glass slide (75 mm x 50 mm) and cover with aluminum foil prior to imaging.

5. Asymmetric PCR for Amplifying ssDNA

1. Prepare an asymmetric PCR reagent mix for amplifying ssDNA to be analyzed. Thaw the reagents in Table 4 on ice. Do not keep the Taq polymerase enzyme (50 U/µL) on ice, but rather store it at -20 °C until needed.
2. Gently vortex all reagents and then briefly centrifuge tubes at 10,000 x g for 10 s.
3. Combine all reagents as described in Table 4.
4. Place samples into a thermocycler and start the asymmetric PCR under the following conditions: 25 cycles (95 °C for 30 s, 52 °C for 30 s, and 72 °C for 30 s), 85 °C for 5 min, hold at 4 °C.

6. Microsphere-PCR for Amplifying ssDNA

Note: This section describes the protocol for amplifying ssDNA in a PCR reaction tube. Microsphere-PCR reactions were performed in 50 μL of reaction volume. The detailed sequences used to amplify ssDNA are listed in Table 5. In this case, Ap on the surface of microspheres can anneal to random DNA templates in a complementary manner. This is a very important step for producing complementary DNA strands (antisense DNA strand, Figure 3). The DNA extended is used as a template for microsphere-PCR amplification.

1. Prepare microsphere-PCR reagent mix. Thaw the reagents in Table 6 on ice; however, do not keep the Taq polymerase enzyme on ice. Store it at -20 °C until needed.
2. Gently vortex all reagents and then briefly centrifuge tubes at 10,000 x g for 10 s.
3. Obtain approximately ~25 microspheres through microscopic counting.
   Note: The number of microspheres in one reaction tube are calculated using a light microscope with 40X magnification. About ~25 microspheres are used for microsphere-PCR amplification. More detailed information is in Step 3.
4. Combine all reagents as described in Table 6.
5. Place samples into a thermocycler and start the asymmetric PCR under the following conditions: 25 cycles (95 °C for 30 s, 52 °C for 30 s, and 72 °C for 30 s), 85 °C for 5 min, hold at 4 °C.
6. Following amplification, add 8 μL of 6x loading buffer and load 15 μL of each sample into 2% agarose gel. Then, perform electrophoresis at 100 V for 35 min in 1x TAE (Tris-acetate-EDTA, 40 mM Tris acetate, 1 mM EDTA, pH 8.2) buffer.

7. Confocal Microscopy Acquisition

Note: The results of microsphere-DNA probe hybridization are imaged under a confocal microscope. Image analysis is performed using ImageJ.

1. Fix hybridized microspheres to the stage of the microscope in a holder.
2. Select the laser (Helium/Neon laser, 543 nm line) and turn it on in laser control.
3. Select the objective lens in microscope control.
4. Select the desired filter for Cy3 and channel in configuration control.
5. Start the experiment and observe the sample. Settings for the confocal microscope are summarized in Table 7.

结果

The fabricated polymeric droplet-based microfluidic platform consists of two PDMS layers (Figure 1a). Three kinds of microfluidic channel networks are used for generating microspheres: 1) Flow-focusing geometry as shown in Figure 1b, 2) a serpentine channel for mixing solution I and solution II, and 3) a polymerization channel for microsphere solidification. The height of all channels was 60 μm. The channel length for mixing and ...

讨论

Contaminants of dsDNA are a major issue in ssDNA amplification. It remains difficult to minimize dsDNA amplification in conventional asymmetric PCR amplification¹⁵. In addition, although technical improvements for generating ssDNA have enabled us to increase the efficiency of sample throughput, ssDNA isolation is still problematic due to its high costs and incomplete purification yields.

Asymmetric PCR is one of the most challenging methods used when working with ssDNA....

材料

本文使用的材料清单

姓名	公司	目录编号	评论
液体聚二甲基硅氧烷，PDMS	Dow Corning Inc.	Sylgard 184	芯片组分
40% 丙烯酰胺：双溶液 （19：1）	Bio-rad	1610140	可共聚寡聚微球
过硫酸铵组分，APS	Sigma Aldrich	A3678	丙烯酰胺固化剂：双溶液
N，N，N′，N′-四甲基乙二胺，TEMED	Sigma Aldrich	T9281	过硫酸铵催化剂
矿物油	Sigma Aldrich	M5904	表 1.解决方案 III.微球试剂
Cy3 标记的互补寡核苷酸探针组	Bioneer	合成	表 3.序列信息
ssDNA 丙烯酸酯标记探针	Bioneer	合成表	1.解决方案 I. 微球试剂
Tris	Biosesang	T1016	TE 缓冲液组分，pH 缓冲溶液
EDTA	Sigma Aldrich	EDS	TE 缓冲液组分，离子去除 （Ca2+）
Ex taq	Takara	RR001A	ssDNA 扩增
共聚焦显微镜	Carl Zeiss	LSM 510	鉴定微球表面的寡核苷酸暴露
光学显微镜	Nikon Instruments Inc.	eclipse 80i	微球计算数量
T100 热循环仪	Bio-rad	1861096	ssDNA 扩增
手持式电晕处理机	Electro-Technic	BD-20AC 实验室电晕处理机	水表面处理
热板	作为一个	HI-1000	加热板，用于液体 PDMS 的固化
注射泵	kd Scientific	78-1100	溶液 I 和溶液 II 的均匀流动
压缩机	Kohands	KC-250A	溶液 III 的流量控制
线血细胞计数器	Sigma Aldrich	Z359629	微球的计算数量