Identifying protein-protein interaction sites using peptide arrays

• Published in: Journal of visualized experiments no. 93; p. e52097
• Main Authors: Amartely, Hadar, Iosub-Amir, Anat, Friedler, Assaf
• Format: Journal Article
• Language: English
• Published: United States MyJove Corporation 18.11.2014
• Subjects: Binding Sites; Molecular Biology; Peptides - chemistry; Peptides - metabolism; Protein Array Analysis - methods; Protein Binding; Protein Interaction Mapping - methods; Protein Structure, Tertiary; Proteins - chemistry; Proteins - metabolism; Signal Transduction
• ISSN: 1940-087X; 1940-087X
• DOI: 10.3791/52097

Protein-protein interactions mediate most of the processes in the living cell and control homeostasis of the organism. Impaired protein interactions may result in disease, making protein interactions important drug targets. It is thus highly important to understand these interactions at the molecular level. Protein interactions are studied using a variety of techniques ranging from cellular and biochemical assays to quantitative biophysical assays, and these may be performed either with full-length proteins, with protein domains or with peptides. Peptides serve as excellent tools to study protein interactions since peptides can be easily synthesized and allow the focusing on specific interaction sites. Peptide arrays enable the identification of the interaction sites between two proteins as well as screening for peptides that bind the target protein for therapeutic purposes. They also allow high throughput SAR studies. For identification of binding sites, a typical peptide array usually contains partly overlapping 10-20 residues peptides derived from the full sequences of one or more partner proteins of the desired target protein. Screening the array for binding the target protein reveals the binding peptides, corresponding to the binding sites in the partner proteins, in an easy and fast method using only small amount of protein. In this article we describe a protocol for screening peptide arrays for mapping the interaction sites between a target protein and its partners. The peptide array is designed based on the sequences of the partner proteins taking into account their secondary structures. The arrays used in this protocol were Celluspots arrays prepared by INTAVIS Bioanalytical Instruments. The array is blocked to prevent unspecific binding and then incubated with the studied protein. Detection using an antibody reveals the binding peptides corresponding to the specific interaction sites between the proteins.