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Method Article

Identifying Protein-protein Interaction Sites Using Peptide Arrays

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DOI:

10.3791/52097

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November 18th, 2014

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In This Article

Summary

Peptide array screening is a high throughput assay for identifying protein-protein interaction sites. This allows mapping multiple interactions of a target protein and can serve as a method for identifying sites for inhibitors that target a protein. Here we describe a protocol for screening and analyzing peptide arrays.

Abstract

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.

Introduction

Protein-protein interactions mediate most of the processes in the living cell. 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. This is because peptides can be easily synthesized and allow the focusing on a specific interactio....

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Protocol

1. Designing a Peptide Array

  1. Divide the sequence of the target protein into partly overlapping 10-20 residues peptides. Vary the amount of overlap on the specific experiment and the resources of the performing lab, but in principle the longer the overlap the better. When designing the peptides take into account known secondary structure elements in the protein that can be responsible for the interaction.
  2. Order the designed peptide array through commercial vendors. Here, use peptides covalently bound to the array through the C-terminus.

2. Blocking Non-specific Binding

  1. Make a 50 mM Tris or Phosphate b....

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Results

STIL is a highly important centrosomal protein. It controls normal cell division and cell proliferation13,15–19. STIL interacts with several proteins 18,20,21, and most of the interactions occur through its central part, which is an intrinsically disordered region (IDR)14. We designed an array composed of peptides derived from the STIL binding protein CHFR. CHFR is a tumor suppressor that is induced in response to mitotic stress22. Since the structure of t.......

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Discussion

Peptide array screening is an excellent tool for identifying the binding sites of a target protein in its partners. This assay is fast and easy to perform and the results can be obtained in one or two working days. Peptide array screening is versatile and can be used for many purposes. It can be used for characterizing post translation modifications such as phosphorylation and identifying substrates of kinases. For example: the FLT3 kinase, which is related to acute myeloid leukemia, phosphorylates Tyr-containing substra.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

AF was supported by a starting grant from the European Research Council under the European Community's Seventh Framework Programme (FP7/2007-2013) / ERC Grant agreement n° 203413 and by the Minerva Center for Bio-hybrid complex systems.HA and AI are supported by the Dalia and Dan Maydan Fellowship for advanced degree students at the Hebrew University of Jerusalem.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Peptide arrayINTAVIS Bioanalytical Instruments
His-probe Antibody (H-3) HRPSanta Cruz Biotechnologysc-8036 HRP
EZ-ECL KitBiological industries20-500-120
Skim MilkBecton, Dickinson and Company232100
LAS-3000 camera FUJI film

References

  1. Benyamini, H., Friedler, A. Using peptides to study protein–protein interactions. Future Medicinal Chemistry. 2 (6), 989-1003 (2010).
  2. Geysen, H. M., Wagner, C. D. Isotope or mass encoding of combinatorial libraries. Chemistry & Biology. 3 (8), 679-688 (....

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