Flow-pattern Guided Fabrication of High-density Barcode Antibody Microarray

Podsumowanie

This protocol outlines the fabrication of a large-scale, multiplexed two-dimensional DNA or antibody array, with potential applications in cell signaling studies and biomarker detection.

Streszczenie

Antibody microarray as a well-developed technology is currently challenged by a few other established or emerging high-throughput technologies. In this report, we renovate the antibody microarray technology by using a novel approach for manufacturing and by introducing new features. The fabrication of our high-density antibody microarray is accomplished through perpendicularly oriented flow-patterning of single stranded DNAs and subsequent conversion mediated by DNA-antibody conjugates. This protocol outlines the critical steps in flow-patterning DNA, producing and purifying DNA-antibody conjugates, and assessing the quality of the fabricated microarray. The uniformity and sensitivity are comparable with conventional microarrays, while our microarray fabrication does not require the assistance of an array printer and can be performed in most research laboratories. The other major advantage is that the size of our microarray units is 10 times smaller than that of printed arrays, offering the unique capability of analyzing functional proteins from single cells when interfacing with generic microchip designs. This barcode technology can be widely employed in biomarker detection, cell signaling studies, tissue engineering, and a variety of clinical applications.

Wprowadzenie

Antibody microarrays have been widely used in proteomic studies for decades to examine the presence of targeted proteins, including protein biomarkers^1-3. Although this field is currently facing great challenges from other high-throughput technologies such as mass spectrometry (MS), there is still plenty of room for the utility of antibody microarrays, mainly because these devices afford simple data interpretation and easy interface with other assays. In recent years, the integration of microarrays into microchip scaffolds has provided the antibody microarray a new opportunity to thrive^4-7. For instance, the barcode microarray integrated into a single-cell microchip has been used in cell communication studies^8,9. This technology has distinctive advantages over other available microarray technologies. It features array elements at 10-100 μm, much smaller than the typical 150 μm size used in conventional microarray elements. The construction of smaller array elements is achieved using systematic flow-patterning approaches, and this gives rise to compact microarrays that can detect single-cell secreted proteins and intracellular proteins. Another advantage is the use of a simple, instrument-free setup. This is particularly important, because most laboratories and small companies may not be able to access microarray core facilities. Such barcode antibody microarrays feature enhanced assay throughput and can be used to perform highly multiplexed assays on single cells while achieving high sensitivity and specificity comparable with that of conventional sandwich enzyme-linked immunosorbent assay (ELISA⁸). This technology has found numerous applications in detecting proteins from glioblastoma^9-11, T cells¹², and circulating tumor cells¹³. Alternatively, barcode DNA microarrays alone have been utilized in the precise positioning of neurons and astrocytes for mimicking the in vivo assembly of brain tissue¹⁴.

This protocol focuses only on the experimental steps and build-up blocks of the two-dimensional (2-D) barcode antibody microarray which has potential applications in the detection of biomarkers in fluidic samples and in single cells. The technology is based on an addressable single-stranded, one-dimensional (1-D) DNA microarray constructed using orthogonal oligonucleotides that are patterned spatially on glass substrates. The 1-D pattern is formed when parallel flow channels are used in the flow-patterning step, and such a pattern appears as discrete bands visually similar to 1-D Universal Product Code (UPC) barcodes. The construction of a 2-D (n x m) antibody array — reminiscent of a 2-D Quick Response (QR) matrix code — needs more complex patterning strategies, but allows for the immobilization of antibodies at a higher density^8,15. The fabrication requires two DNA patterning steps, with the first pattern perpendicular to the second. The points of intersection of these two patterns constitute the n x m elements of the array. By strategically selecting the sequences of single-stranded DNA (ssDNA) utilized in flow-patterning, each element in a given array is assigned a specific address. This spatial reference is necessary in distinguishing between fluorescence signals on the microarray slide. The ssDNA array is converted into an antibody array through the incorporation of complementary DNA-antibody conjugates, forming a platform called DNA-encoded antibody library (DEAL¹⁶).

This video protocol describes the key steps in creating n x m antibody arrays which include preparing polydimethylsiloxane (PDMS) barcode molds, flow-patterning ssDNA in two orientations, preparing antibody-oligonucleotide DEAL conjugates, and converting the 3 x 3 DNA array into a 3 x 3 antibody array.

Protokół

Caution: Several chemicals used in this protocol are irritants and are hazardous in case of skin contact. Consult material safety data sheets (MSDS) and wear appropriate personal protective equipment before performing this protocol. The piranha solution used in Step (1.1.1) is highly corrosive and should be prepared by adding the peroxide slowly to the acid with agitation. Handle this solution with extreme caution in a fume hood. Use appropriate eye protection and acid-resistant gloves. Trimethylchlorosilane (TMCS) is a corrosive, flammable chemical used in an optional step after (1.1.6). Handle this chemical in a fume hood.

Note: Perform the barcode slide fabrication and critical flow-patterning procedures in a clean room to minimize contamination by particulate matter. Dust particles may block the ports and microchannels of PDMS molds and interfere with flow-patterning.

1. Construction of the One-dimensional DNA Barcode Slide

1. Preparation of the SU-8 master for barcode flow patterns
   Note: The drawings for the perpendicular flow patterns (Figure 1A-B) are created using a computer-aided design (CAD) software. These patterns are rendered on a chrome photomask. Transparent areas of the mask correspond to the features of the SU-8 master.
   1. Clean a silicon wafer (100 mm diameter) thoroughly in a mixture of 3 H₂SO₄: 1 30% H₂O₂ (piranha solution) heated to 96 °C. Wash the wafer with deionized water and isopropyl alcohol, followed by drying with a nitrogen blow gun.
   2. Pour about 4 ml of SU-8 2025 photoresist on the wafer. Use a programmable spin coater to uniformly spread the photoresist on the wafer for 10 sec at 500 rpm, then 30 sec at 3,000 rpm. This creates a photoresist layer with a thickness of ~25 µm. Gradually allow spinning to slow down before stopping — this is to maintain an even coating on the wafer's surface.
   3. Bake the coated wafer on a hotplate for 1 min at 65 °C, then for 5 min at 95 °C. This step allows the coating to solidify. Cool to RT for 5 min.
   4. Place the chrome mask (Figure 1C) on the photoresist coat. Expose the mask features to near-UV light (350-400 nm, exposure energy 150-160 mJ/cm²) for 20 sec.
      Note: The design on the chrome mask contains 20 channels, each of which are 20 µm wide with 50 µm pitch. The channels are winding from one end of the pattern to the opposite end. Altogether, the 20 channels cover a rectangular area with a length of ~40 mm and a width of ~20 mm. Each channel is flanked by two circular features which correspond to an inlet and an outlet. Inlets and outlets are interchangeable.
   5. Bake the exposed wafer on a hotplate for 5 min at 95 °C. Cool to RT gradually.
   6. Immerse the wafer in SU-8 developer with agitation for 5 min. Wash the wafer with a small portion of fresh SU-8 developer, followed by isopropyl alcohol. Dry the wafer using a nitrogen blow gun. Hard-bake the wafer on a 200 °C hotplate for 30 min, and allow the wafer to cool gradually to RT.
      Note: Development may be carried out for a longer time if a white film is observed after washing in this step.
      Optional: Silanize the SU-8 master by exposing it to trimethylchlorosilane vapor in a closed Petri dish for 10 min.
2. Preparation of the PDMS barcode mold
   1. Combine 40.0 g silicone elastomer base with 4.0 g curing agent. Stir the prepolymer mixture vigorously for 10 min. Degas for 20 min under vacuum.
      Note: As a general rule, use a 10:1 (base: curing agent) mass ratio.
   2. Pour the prepolymer into a Petri dish containing a silicon wafer with the SU-8 master of the barcode pattern. The height of the PDMS mixture should be about 7.5 mm or above. Degas the mixture in the Petri dish for a second time to remove any remaining bubbles, then bake the mixture for 1 hr at 75 °C to allow PDMS to cure.
      Note: It is important to maintain enough thickness of the PDMS slab at ~7.5 mm or above to avoid adding too much tension to the PDMS-glass bond upon insertion of pins/tubing through holes in the PDMS mold in step (1.3.3.1)
   3. Using a scalpel, carefully cut around the area of the PDMS slab that contains the barcode mold features and peel the slab from the wafer.
   4. Trim the edges of the slab to attain the desired shape of the PDMS barcode mold. Punch 20 holes (1.0-mm diameter) through the mold using a biopsy punch with plunger. Ensure that the holes are aligned with the circular features of the barcode pattern. These holes serve as the inlets and outlets.
3. One-dimensional patterning of poly-L-lysine (PLL)
   1. Remove any dust on the surface of a poly-L-lysine coated glass slide using a nitrogen blow gun. Attach the PDMS mold to the clean glass slide. Ensure that the edges of the mold and the slide are aligned.
   2. Bake for 1.5 hr at 75 °C to strengthen the bond between the PDMS mold and the PLL-coated slide. Meanwhile, prepare 20 pieces of flexible polyethylene tubing (3- to 4-inch pieces, with an inner diameter of 0.5 mm and an outer diameter of 1.5 mm).
      Note: The number of pieces of tubing corresponds to the number of inlets in the PDMS barcode mold. The tubing serves to couple the channels on the PDMS barcode mold to a nitrogen gas tank equipped with a pressure regulator.
   3. To one end of each piece of tubing, attach a stainless steel hollow pin (1-mm diameter). Aspirate sterile-filtered poly-L-lysine solution through the pin, until at least 1 cm of the tubing is filled with the solution.
      1. Fasten the pins (connected to solution-filled tubing) to the inlets of the PDMS barcode mold (Figure 1E). Attach the other end of the tubes to a pressure-regulated nitrogen tank set-up. Allow the solution to flow through the mold using a pressure range of 0.5-1 psi for at least 6 hr.
         Note: Refer to step (1.3.3) for all flow-patterning procedures.
4. One-dimensional patterning of ssDNA ¹⁴
   Note: The phosphate buffered saline (PBS) used in subsequent steps is prepared from 137 mM NaCl, 10 mM Na₂HPO₄, and 2 mM KH₂PO_4. The pH of the buffer is 7.4.
   1. Prepare 2 mM bis(sulfosuccinimidyl)suberate (BS3) solution in PBS. Prepare 300 µM solutions of A, B, and C ssDNA (5'-amine modified, 80 nucleotides) in PBS or ultrapure water.
      Note: Use the BS3 solution within about 30 min after preparation because the N-hydroxysuccinimide ester easily undergoes hydrolysis.
   2. Combine 2.5 µl of 300 µM A, B, or C ssDNA with 2.5 µl of 2 mM bis(sulfosuccinimidyl)suberate in PBS for each channel. A, B, and C DNA are designated to channels 1, 2, and 3, respectively. This order is also applied to remaining sets of 3 channels (Figure 2A).
   3. Perform step (1.3.3). This time, aspirate the 5-µl BS3/DNA solutions through stainless steel pins and into the polyethylene tubing, then couple the PDMS mold to the nitrogen source. Allow the BS3/DNA solution to flow through the barcode mold for about 40 min or until at the channels are filled.
   4. Stop the flow once all channels are filled, then incubate the BS3/DNA solution in the barcode at RT for 2 hr. Do not allow the solution to dry up. Bake the PDMS mold with attached barcode slide for 1 hr at 75 °C.
      Note: To facilitate alignment in subsequent flow-patterning steps, the edges of the channel pattern on the barcode slide may be outlined. This is done by carefully scratching the glass surface using a diamond scribe to generate alignment markers on the bottom of the glass slide. Alignment in later stages of the protocol may be checked under a microscope.
   5. Remove the PDMS mold from the barcode slide. Wash the slide gently with 0.01% SDS once and three times with ultrapure water.
      1. Dry the barcode slide using a microscope slide spinner. Store the barcode slide in a clean 50-ml centrifuge tube for subsequent use.

2. Validation of the One-dimensional Pattern on the Barcode Slide

Note: This validation protocol may also be adapted for use in assessing the quality of subsequent flow patterning steps.

1. Blocking of the slide
   1. Prepare 1% bovine serum albumin (BSA) in PBS. Filter this solution through a 0.45 µm syringe filter before use. Using a gel-loading tip, apply 50 µl of 1% BSA solution to one edge of the barcode slide.
   2. Incubate the 1% BSA solution for 1 hr at RT.
2. Incubation with Cyanine 3 (Cy3)-conjugated complementary DNA
   1. Prepare a cocktail of A', B', and C' oligonucleotides conjugated to Cy3 at one end. The sequences of A', B', and C' are complementary to those of A, B, and C, respectively. The working concentration of the Cy3-DNA is 0.05 µM in 0.1% BSA.
   2. Remove the BSA solution from the slide by pipetting, then apply 30 µl of the DNA cocktail solution on the same edge of the slide. Incubate the Cy3-DNA cocktail on the slide at RT for 1 hr. Perform this incubation step in the dark to protect the Cy3 moiety from photobleaching.
3. Analysis of fluorescence intensity
   1. Pipette out the Cy3-DNA cocktail and wash the slide in 1% BSA, PBS, and finally in diluted PBS (1 part PBS with 50 parts ultrapure water). Dry the slide using a spinner.
   2. Observe the fluorescence (Figure 2B) using a fluorescence microscope or a microarray scanner. When using a microarray scanner, set the laser emission wavelength to 532 nm, the pixel size at 5 microns, photomultiplier tube (PMT) gain at 450 and power at 15%.

3. Fabrication of the 2-dimensional (3x3) DNA Array¹⁴

1. Preparation of the PDMS barcode mold
   1. Perform procedure (1.1) to construct another SU-8 master, but this time use a chrome mask with a flow pattern perpendicular to that of the first design. Perform procedure (1.2) to construct a new PDMS mold with the perpendicular pattern.
2. Two-dimensional flow patterning of ssDNA
   1. For a 3 x 3 array, prepare 150 µM stock solutions of A'-i, B'-ii, C'-iii, A'-iv, B'-v, C'-vi, A'-vii, B'-viii, and C'-ix DNA in 3% BSA/PBS. These oligonucleotides serve as "bridging sequences" (Figure 2A). Combine the oligonucleotide solutions (Solutions 1 to 3) such that the working concentration is 50 µM for each oligonucleotide. Use the guide provided in Table 1.
   2. Flow 3% BSA/PBS blocking solution into all 20 channels for 1 hr at 0.5-1 psi.
   3. Flow Solutions 1, 2, and 3 into channels 1, 2, and 3, respectively. Follow this order for subsequent sets of 3 channels. Flow is usually completed in around 40 min. Incubate the DNA solutions at RT for 2 hr to allow the DNA to hybridize.
   4. Flow 3% BSA/PBS blocking solution into all 20 channels for 1 hr at 0.5-1 psi to remove unhybridized DNA. Peel off the PDMS slab, and wash the resulting DNA microarray slide by dipping the glass slide into 3% BSA/PBS once and PBS twice, followed by diluted PBS (1 part PBS and 50 parts ultrapure water). Dry the slide using a microscope slide spinner.
   5. Perform a second validation step (Figure 2C) similar to that in section 2. Use oligonucleotides i' to ix' that are Cy3-conjugated. Store the 3 x 3 array slide in a 50-ml centrifuge tube for subsequent use.
      Note: The DNA microarray can be stored at RT in a desiccator for months.

4. Conversion of the 3 x 3 DNA Array into an Antibody Array

1. Preparation of antibody-oligonucleotide (DEAL) conjugates
   1. Prepare solutions of 200 mM succinimidyl-4-formylbenzoate (S-4FB) and 40 mM succinimidyl-6-hydrazinonicotinamide (S-HyNic) in anhydrous N,N-dimethylformamide (DMF).
   2. Prepare up to 7 separate solutions of capture antibodies (1 mg/ml) in PBS.
      Note: If the antibody stock solutions contain sodium azide bacteriostat, perform buffer exchange with PBS using spin desalting columns with 7 kDa molecular weight cut-off (MWCO).
   3. Prepare separate 400 µM solutions of i', ii', iii', iv', v', vi', and vii' DNA. Assign each capture antibody to one oligonucleotide sequence. Combine 40 µl of 400 µM DNA with 12.25 µl of DMF in microcentrifuge tubes and spin down to mix thoroughly.
      1. To each DNA/DMF solution, add 2.3 µl of 200 mM S-4FB in DMF. For every 100 µg of capture antibody, add 2.25 µl of 40 mM S-HyNic in DMF.
   4. Incubate the antibody/S-HyNic and DNA/S-4FB solutions for 4 hr at RT.
   5. In preparation for the antibody-DNA coupling reaction, prepare new spin desalting columns (one for each DNA solution and one for each antibody) by washing them with citrate buffer at pH 6.
   6. After 4 hr of incubation, perform buffer exchange for each antibody/S-HyNic and DNA/S-4FB solution. Combine the S-4FB-conjugated i', ii', iii', iv', v', vi' and vii' oligonucleotides with the antibody-S-HyNic conjugates. Incubate the mixtures for 2 hr at RT.
   7. Incubate the reaction O/N at 4 °C.
2. Purification of antibody-oligonucleotide (DEAL) conjugates
   Note: To purify the antibody-oligonucleotide conjugates, perform fast protein liquid chromatography (FPLC) on a standard FPLC system equipped with a Superose 6 10/300 GL column.
   1. Set the wavelength of UV detector of the FPLC system to 280 nm. Use isocratic flow of PBS (pH 7.4) at 0.3 ml/min to separate the antibody-oligonucleotide conjugates from the excess S-4FB-DNA.
   2. Pool the fractions containing the conjugate and concentrate the fractions to a volume of 150 µl using spin filters with a 10 kDa MWCO.
3. Two-dimensional patterning of antibodies
   1. Prepare another PDMS mold with microchambers or micro-wells using fabrication procedures in step (1.2). The PDMS mold may contain microliter to nanoliter wells for immunoassays.
      Note: For general biomarker detection in fluidic samples, a PDMS mold with multiple wells is mated with the array slide. The features of the PDMS mold depend on the system being studied. For instance, the detection of proteins from single cell experiments can be performed with a PDMS mold containing microchambers with 0.15-nl volumes.
   2. (Optional) Subject the PDMS mold to plasma cleaning (18 W) for 1.5 min to render its patterned surface hydrophilic. Prior to plasma cleaning, use adhesive tape to block all other surfaces that will be directly bonded to the 3 x 3 array slide.
      Note: Step (4.3.2) is optional but is usually performed when the PDMS mold is intended for use in single cell experiments.
   3. Mate the PDMS mold with the 3 x 3 array slide, then block the slide with 1% BSA in PBS. Incubate for 1 hr at RT. Meanwhile, prepare a cocktail (200 µl final volume) of antibody-oligonucleotide conjugates. The working concentration of each conjugate is 10 µg/ml in 1% BSA/PBS.
   4. Add the antibody-oligonucleotide cocktail, then incubate for 1 hr at 37 °C to allow the oligonucleotide moiety of the conjugates to hybridize with specific spots on the 3 x 3 arrays, thereby converting the DNA array to an antibody array.
   5. Repeat step (3.2.4) to clean and dry the slide. The highest sensitivity can be achieved if the antibody array is used immediately. Prolonged storage may result in loss of sensitivity.
4. Detection of proteins
   1. Reconstitute recombinant proteins or prepare a filtered cell sample.
   2. Mate the microarray with a custom-designed chip, and block the surface with 3% BSA in PBS for 1 hr. Then remove the BSA solution, and apply samples and incubate for 2 hr.
   3. Wash off the samples using 3% BSA in PBS three times, and then add detection antibodies at a concentration provided by the product datasheet. Incubate for 2 hr.
   4. Wash off the detection antibodies by 3% BSA in PBS three times, and then add Cyanine 5(Cy5)-streptavidin at 1 µg/ml, followed by incubation for 1 hr.
   5. Repeat step (3.2.4) to clean and dry the slide for scanning.

Wyniki

The designs for the PDMS molds (Figure 1A-1B) were drawn using a CAD program (AutoCAD). Two designs shown feature channels for flow patterning, one horizontal and one vertical. The left and right parts of each design are symmetric; either of them could be inlets or outlets. Each of 20 channels is winding from one end all the way to the other end. Each design is printed on a chrome photomask (Figure 1C). The fabricated SU-8 master on a wafer is shown in

Dyskusje

Flow pattern design is the first critical step in fabricating the 2-D microarray. To generate two overlapping DNA patterns on a glass substrate, the channel features of the first design should be perpendicular to those of the second (Figure 1A-B). The designs also consider the downstream applications of the microarray. In the case of single cell analysis, the microarray is used to detect proteins from single cells enclosed in microchambers, therefore the channel dimensions are made compatible wi...

Materiały

Name	Company	Catalog Number	Comments
Sylgard 184 silicone elastomer base	Dow Corning	3097366-1004
Sylgard 184 silicone elastomer curing agent	Dow Corning	3097358-1004
SU-8 2025 photoresist	MicroChem	Y111069
Silicon wafers	University Wafers	452
Poly-L-lysine coated glass slides	Thermo Scientific	C40-5257-M20
Oligonucleotides	Integrated DNA Technologies		*Custom-ordered from Integrated DNA Technologies, see Table 2.
Poly-L-lysine adhesive stock solution	Newcomer Supply	1339
Bis (sulfosuccinimidyl) suberate  (BS3)	Thermo Scientific	21585
1x Phosphate buffered saline, pH 7.4	Quality Biological	114-058-101
Äkta Explorer 100 Fast Protein Liquid Chromatography (FPLC) System	GE (Amersham Pharmacia)	18-1112-41
Superose 6 10/300 GL column	GE Healthcare Life Sciences	17-5172-01
Capture antibodies	various	various	*Antibody selection depends on application
Succinimidyl-6-hydrazino-nicotinamide (S-HyNic)	Solulink	S-1002
Succinimidyl-4-formylbenzamide (S-4FB)	Solulink	S-1004
N,N-dimethylformamide	Sigma-Aldrich	227056
Citric acid, anhydrous	Acros	42356
Sodium hydroxide	Fisher Scientific	S318
Amicon Ultra spin filter 10 kDa MWCO	EMD Millipore	UFC201024
Spin coater	Laurell Technologies	WS-650-MZ
Biopsy punch with plunger (1.0 mm diameter)	Ted Pella, Inc.	15110-10
Diamond scribe (Style 60)	SPI supplies	6004
Trimethylchlorosilane	Sigma Aldrich	92361