Luciferase Complementation Assay for Protein-Protein Interactions in Plants

Curr Protoc Plant Biol. 2018 Mar;3(1):42-50. doi: 10.1002/cppb.20066.

Abstract

Constitutive and dynamic protein-protein interactions are fundamental to all aspects of cellular processes. Compared to other techniques measuring protein-protein interactions in plants, the luciferase complementation assay has a number of advantages: it detects plant protein-protein interactions in real time, requires little hands-on manipulation of samples, is highly quantitative, has extremely low background, and can be easily scaled up for high-throughput interactome studies. Here, we describe a protocol that includes two alternate data collection methods to quantify luminescence results based on Agrobacterium-mediated transient luciferase expression in Nicotiana benthamiana. One data collection method employs a charge-coupled device imaging system that allows the interactions to be presented as images, and the other employs a luminometer, which enables the assay to be conducted in a 96-well plate. Technical parameters related to frequently encountered problems and common errors, presented here, are important for performing this assay successfully. © 2018 by John Wiley & Sons, Inc.

Keywords: Nicotiana benthamiana; interactome; luciferase complementation assay; protein-protein interactions; split luciferase assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agrobacterium / genetics*
  • Genetic Complementation Test
  • Luciferases / genetics*
  • Nicotiana / enzymology
  • Nicotiana / genetics*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Protein Interaction Mapping*

Substances

  • Plant Proteins
  • Luciferases