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Protein microarrays for identification of novel extracellular protein-protein interactions.

Current protocols in protein science (2013-04-03)
Irene Tom, Nicholas Lewin-Koh, Sree R Ramani, Lino C Gonzalez
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.

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Sigma-Aldrich
Protein A from Staphylococcus aureus, Soluble, Cowan strain, recombinant, expressed in E. coli, aqueous solution, ≥95% (HPLC)