Method Article

Measuring Transcellular Interactions through Protein Aggregation in a Heterologous Cell System

DOI:

10.3791/61237

May 22nd, 2020

In This Article

Summary

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Here, we present an optimized protocol to rapidly and semiquantitatively measure ligand-receptor interactions in trans in a heterologous cell system using fluorescence microscopy.

Abstract

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Protein interactions at cellular interfaces dictate a multitude of biological outcomes ranging from tissue development and cancer progression to synapse formation and maintenance. Many of these fundamental interactions occur in trans and are typically induced by heterophilic or homophilic interactions between cells expressing membrane anchored binding pairs. Elucidating how disease relevant mutations disrupt these fundamental protein interactions can provide insight into a myriad of cell biology fields. Many protein-protein interaction assays do not typically disambiguate between cis and trans interactions, which potentially leads to an overestimation of the extent of binding that is occurring in vivo and involve labor intensive purification of protein and/or specialized monitoring equipment. Here, we present an optimized simple protocol that allows for the observation and quantification of only trans interactions without the need for lengthy protein purifications or specialized equipment. The HEK cell aggregation assay involves the mixing of two independent populations of HEK cells, each expressing membrane-bound cognate ligands. After a short incubation period, samples are imaged and the resulting aggregates are quantified.

Introduction

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Synaptic interactions facilitated by synaptic adhesion molecules are foundational for the development, organization, specification, maintenance and function of synapses and the generation of neural networks. The identification of these transsynaptic cell adhesion molecules is rapidly increasing; thus, it is fundamentally important to identify binding partners and understand how these new adhesion molecules interact with each other. Additionally, genome sequencing has identified mutations in many of these adhesion molecules that are commonly linked to a multitude of neurodevelopmental, neuropsychiatric, and addiction disorders1. Mutations in gen....

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Protocol

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1. Cell culture and transfection

  1. Make HEK cell media with DMEM, 1x (Dulbecco's Modification of Eagle's Medium) supplemented with 4.5 g/L glucose, L-glutamine & sodium pyruvate and 10% FBS. Sterile filter.
  2. Predetermine suitable ligands and receptors for aggregation assay.
    NOTE: Neurexin3α SS4+/- and one of its known ligands, LRRTM2, were used in this study. Ligands and receptors of interest were expressed from cDNAs in pcDNA3.1. A Gibson assembly was used to insert Neurexin3α into pcDNA3.112. Neurexin3α F/R: TTTAAACTTAAGCTTGGTACCGAGCTCGGATCCGCCACCATGAGCTTTACCCTCCACTC/
    GAGCGGCCGCCACTG....

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Results

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The A687T mutation increases Neurexin3α SS4- binding to LRRTM27
To investigate how intercellular interactions of two known synaptic proteins are affected by the introduction of a point mutation found in a patient with intellectual disability and epilepsy, we used the above HEK cell aggregation assay (Figure 1). Cells were transfected according to section 1 and prepared for imaging according to sections 1 and 2 of the protocol. Cells were imaged at baseline whe.......

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Discussion

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Dissecting the protein-protein interactions that occur in trans during cell adhesion can lead to a better understanding of the molecular mechanisms underlying basic cellular processes including the formation, function and maintenance of synapses during maturation and remodeling. The implications of cell-to-cell interactions expand beyond neurobiology and have broader roles in signal transduction, cell migration and tissue development14. Aberrations in cell adhesion can disrupt cellular processes i.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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This work was supported by Grants from the National Institute of Mental Health (R00MH103531 and R01MH116901 to J.A.), a predoctoral training Grant from the National Institute of General Medicine (T32GM007635 to S.R.), and a Lyda Hill Gilliam Fellowship for Advanced Study (GT11021 to S.R.). We thank Dr. Kevin Woolfrey for help with the microscope, Dr. K Ulrich Bayer for the use of his epifluorescent microscope, and Thomas Südhof (Stanford University) for the LRRTM2 plasmid.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1.5 mL disposable microtubes with snap capsVWR89000-028Incubation of mixed population of HEK cells
1000 mL Rapid—Flow Filter Unit, 0.2 um aPES membraneThermo Fisher567-0020Sterilization of HEK media
15 mL SpectraTube centrifuge tubesWard’s Science470224-998Harvesting HEK cells
6 well sterile tissue culture platesVWR100062-892culturing HEK cells
Calcium ChlorideSigma223506-500GCalcium phosphate transfection, HEK cell resuspension
Centrifuge- Sorvall Legend RTKendro Laboratory Products75004377Harvesting HEK cells
CO2 cell incubatorThermo ScientificHERACELL 150iIncubation of HEK cells during growth
DMEM, 1x (Dulbecco's Modification of Eagle's Medium) with 4.5 g/L glucose, L-glutamine & sodium pyruvateCorning10-013-CVHEK cell maintenance
Dulbecco’s Phosphate Buffered Saline PBS (1X)Gibco14190-144Passaging/harvesting HEK cell
Ethylenediaminetetraacetic acidSigmaED-500GHarvesting HEK cells
Falcon Vented culture flasks, 75cm2 growth areaCorning9381M26Culturing HEK cells
Fetal Bovine SerumSigma17L184HEK cell maintenance
HEK293T cellsATCCModel system
ImageJNIHV: 2.0.0-rc-69/1.52pImage analysis
Magnesium Chloride hexahydrateSigmaM9272-500GHEK cell resuspension
Sodium phosphate dibasic anhydrousFisher BioReagentsBP332-500Calcium phosphate transfection
Trypsin 0.25% (1X) SolutionGE Healthcare Life SciencesSH30042.01Passaging HEK cells
Tube rotatorIncubation of mixed population of HEK cells
UltraClear Microscope slides. White Frosted, Positive ChargedDenville Scientific Inc.M1021Image acquisition
Wide-field microscopeZeissAxio Vert 200MImage acquisition

References

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  1. Südhof, T. C. Neuroligins and neurexins link synaptic function to cognitive disease. Nature. 455 (7215), 903-911 (2008).
  2. Lakey, J. H., Raggett, E. M. Measuring protein-protein interactions. Current Opinion in Structural Biology. 8 (1), 119-123 (1998).
  3. ....

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Tags

Transcellular InteractionsProtein AggregationHEK Cell AggregationTrans Adhesion AssayFluorescence ImagingCell CountingEDTA TreatmentCentrifugation ProtocolGFP mCherry LabelingAdhesion Molecule Screening

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