Unit
UNIT 27.3 Protein Microarrays for Identification of Novel Extracellular Protein-Protein Interactions
Published Online: 1 APR 2013
DOI: 10.1002/0471140864.ps2703s72
Copyright © 2013 by John Wiley & Sons, Inc.
Lab Protocol Title

Current Protocols in Protein Science
Additional Information
How to Cite
Tom, I., Lewin-Koh, N., Ramani, S. R. and Gonzalez, L. C. 2013. Protein Microarrays for Identification of Novel Extracellular Protein-Protein Interactions. Current Protocols in Protein Science. 72:27.3:27.3.1–27.3.24.
Publication History
- Published Online: 1 APR 2013
- Published Print: APR 2013
- Abstract
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Abstract
Functional protein microarrays offer the capability for high-throughput protein interaction analysis and have long promised to be a powerful tool for understanding protein interactions at the proteome scale. Although popular techniques for protein-protein interaction mapping like yeast-two-hybrid and affinity-purification mass spectrometry have performed well for identifying intracellular protein-protein interactions, the study of interactions between extracellular proteins has remained challenging for these methods. Instead, the use of protein microarrays appears to be a robust and efficient method for the identification of interactions among the members of this class of protein. This unit describes methods for extracellular protein microarray production, screening, and analysis. A protocol is described for enhanced detection of low-affinity interactions by generating multivalent complexes using Fc-fusion bait proteins and protein A microbeads, along with a statistical method for hit scoring and identification of nonspecific interactions. Curr. Protoc. Protein Sci. 72:27.3.1-27.3.24. © 2013 by John Wiley & Sons, Inc.
Keywords:
- protein microarray;
- microarray analysis;
- extracellular protein;
- multivalent binding;
- protein-protein interaction
