Method Article

Split Luciferase Complementation Assay to Identify Specific Protein-Protein Interactions

July 8th, 2025

In This Article

Abstract

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Source: Wiertelak, W. et.al., Demonstration of Heterologous Complexes formed by Golgi-Resident Type III Membrane Proteins using Split Luciferase Complementation Assay. J. Vis. Exp. (2020)

This video demonstrates the split luciferase complementation assay to detect protein-protein interactions. In this assay, the proteins of interest are tagged to small and large fragments of the luciferase enzyme. When the proteins interact, the large and small fragments combine to form an active enzyme complex, which in the presence of a specific substrate, releases bright luminescence that can be measured.

Protocol

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1. Transient transfection of the expression plasmids into the cells

  1.  Harvest the adherent HEK293T cell culture by trypsinization and resuspend the cells in a dedicated complete growth medium. Plate the cells (2 x 104/100 µL/well) onto a clear bottom, white side 96-well plate. Adjust the total number of wells to accommodate all tested combinations and controls including replicates.
    NOTE: Attempt to use only the inner 60 wells of the plate to minimize thermal shifts and avoid overnight evaporation. Using poly-D-lysine-coated plates is highly recommended such as the ones indicated in the Table of Materials<....

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
0.25% trypsin-EDTA solutionCell culture
Adherent mammalian cell lineCell culture
BioCoat Poly-D-Lysine 96-well White/Clear Flat Bottom TC-treated Microplate, with LidCorning356651Plastic ware
Cell culture centrifugePlastic ware
Cell culture supplements (heat-inactivated fetal bovine serum, L-glutamine, penicillin, streptomycin)Cell culture
CO2 incubatorDevice
Expression plasmids encoding protein(s) of interest not tagged with NanoBiT fragmentsAssay
FuGENE HD Transfection ReagentPromegaE2311Assay
GloMax Discover Microplate Reader (or a different luminescence microplate reader)PromegaGM3000Device
Growth medium dedicated to the cell line usedCell culture
Materials and reagents for standard molecular cloning (bacteria, thermostable polymerase, restriction enzymes, DNA ligase, materials and reagents for nucleic acid purification)Assay
NanoBiT MCS Starter SystemPromegaN2014This kit contains vectors enabling tagging of the proteins of interest with NanoBiT fragments at different orientations as well as the control plasmid encoding HaloTag protein fused with SmBiT and a positive control plasmid pair.
Nano-Glo Live Cell Assay SystemPromegaN2011This kit contains furimazine, which is a substrate enabling detection of the NanoLuc activity in living cells, and a dedicated dilution buffer.
Opti-MEM I Reduced Serum Medium, no phenol redGibco11058021Cell culture
Orbital shakerDevice

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Tags

Transmembrane ProteinsLuciferase Enzyme FragmentsFurimazine SubstrateMicroplate ReaderHEK293T Cell CultureSerum Free MediumLuminescence MeasurementPlasmid Transfection

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