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Method Article

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

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DOI:

10.3791/53644

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January 6th, 2016

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In This Article

Summary

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.

Abstract

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.

Introduction

Antibody microarrays have been widely used in proteomic studies for decades to examine the presence of targeted proteins, including protein biomarkers1-3. 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 thrive4-7. For instance, the barcode microarray integrated into a s....

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Protocol

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 t....

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Results

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

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Discussion

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.......

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Disclosures

The authors have no competing interests to disclose.

Acknowledgements

The authors would like to acknowledge the startup fund from SUNY Albany and the access of facilities at the University at Albany Cancer Research Center.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Sylgard 184 silicone elastomer baseDow Corning3097366-1004
Sylgard 184 silicone elastomer curing agentDow Corning3097358-1004
SU-8 2025 photoresistMicroChemY111069
Silicon wafers University Wafers452
Poly-L-lysine coated glass slidesThermo ScientificC40-5257-M20
OligonucleotidesIntegrated DNA Technologies*Custom-ordered from Integrated DNA Technologies, see Table 2.
Poly-L-lysine adhesive stock solutionNewcomer Supply1339
Bis (sulfosuccinimidyl) suberate  (BS3)Thermo Scientific21585
1x Phosphate buffered saline, pH 7.4Quality Biological114-058-101
Äkta Explorer 100 Fast Protein Liquid Chromatography (FPLC) SystemGE (Amersham Pharmacia) 18-1112-41
Superose 6 10/300 GL columnGE Healthcare Life Sciences17-5172-01
Capture antibodiesvariousvarious*Antibody selection depends on application
Succinimidyl-6-hydrazino-nicotinamide (S-HyNic)SolulinkS-1002
Succinimidyl-4-formylbenzamide (S-4FB)SolulinkS-1004
N,N-dimethylformamideSigma-Aldrich227056
Citric acid, anhydrousAcros42356
Sodium hydroxideFisher ScientificS318
Amicon Ultra spin filter 10 kDa MWCOEMD MilliporeUFC201024
Spin coaterLaurell TechnologiesWS-650-MZ
Biopsy punch with plunger (1.0 mm diameter)Ted Pella, Inc.15110-10
Diamond scribe (Style 60)SPI supplies6004
TrimethylchlorosilaneSigma Aldrich92361

References

  1. Alhamdani, M. S. S., Schroder, C., Hoheisel, J. D. Oncoproteomic profiling with antibody microarrays. Genome Med. 1 (7), (2009).
  2. Angenendt, P. Progress in protein and antibody microarray technology. Drug Discov Today. 10 (7), 503-511 (2005).
  3. Sun, H. Y., Chen, G. Y. J., Ya....

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