| Literature DB >> 30040251 |
Zhaoyang Zhou1, Guozhi Bi1, Jian-Min Zhou1.
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.Entities:
Keywords: Nicotiana benthamiana; interactome; luciferase complementation assay; protein-protein interactions; split luciferase assay
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Year: 2018 PMID: 30040251 DOI: 10.1002/cppb.20066
Source DB: PubMed Journal: Curr Protoc Plant Biol