A subscription to JoVE is required to view this content. Sign in or start your free trial.

Method Article

A Yeast 2-Hybrid Screen in Batch to Compare Protein Interactions

13.7K views

⸱

DOI:

10.3791/57801

⸱

June 6th, 2018

 ,  , 

In This Article

Summary

Batch processing of yeast 2-hybrid screens allows for direct comparison of the interaction profiles of multiple bait proteins with a highly complex set of prey fusion proteins. Here, we describe refined methods, new reagents, and how to implement their use for such screens.

Abstract

Screening for protein-protein interactions using the yeast 2-hybrid assay has long been an effective tool, but its use has largely been limited to the discovery of high-affinity interactors that are highly enriched in the library of interacting candidates. In a traditional format, the yeast 2-hybrid assay can yield too many colonies to analyze when conducted at low stringency where low affinity interactors might be found. Moreover, without a comprehensive and complete interrogation of the same library against different bait plasmids, a comparative analysis cannot be achieved. Although some of these problems can be addressed using arrayed prey libraries, the cost and infrastructure required to operate such screens can be prohibitive. As an alternative, we have adapted the yeast 2-hybrid assay to simultaneously uncover dozens of transient and static protein interactions within a single screen utilizing a strategy termed DEEPN (Dynamic Enrichment for Evaluation of Protein Networks), which incorporates high-throughput DNA sequencing and computation to follow the evolution of a population of plasmids that encode interacting partners. Here, we describe customized reagents and protocols that allow a DEEPN screen to be executed easily and cost-effectively.

Introduction

A complete understanding of cell biological processes relies on finding the protein interaction networks that underlie their molecular mechanisms. One approach to identify protein interactions is the yeast 2-hybrid (Y2H) assay, which works by assembling a functioning chimeric transcription factor once two protein domains of interest bind to one another1. A typical Y2H screen is performed by creating a population of yeast that houses both a library of plasmids encoding interacting proteins fused to a transcriptional activator (e.g., 'prey' fusion protein) and a given 'bait' plasmid comprised of the protein of interest fu....

Access restricted. Please log in or start a trial to view this content.

Protocol

1. Preparation of Media and Plates

NOTE: All plates need to be made minimally 2 days before beginning the protocol. The media can be made at any point. However, the buffered yeast extract peptone dextrose adenine (bYPDA) needs to be made the day of which it will be used. Some media is made using a supplement mix containing a level of adenine that is larger than what is typically used. Most minimal media supplements specify 10 mg/L adenine. Supplements labeled '+40Ade' specify a total of 40 mg/L adenine.

  1. Prepare Glucose Solution (50% w/v). For 1 L, dissolve 500 g of D-(+)-Glucose in 800 mL of distilled wa....

Access restricted. Please log in or start a trial to view this content.

Results

The Y2H assay has been widely used for finding protein:protein interactions and several adaptations and systems have been developed. For the most part, the same considerations that help ensure success with these previous approaches are important for DEEPN. Some of the important benchmarks include: ensuring expression of DNA-binding domain fusion proteins, ensuring a low background of spurious His+ growth in the diploids containing the bait of interest with an empty prey plasmid, a high ma.......

Access restricted. Please log in or start a trial to view this content.

Discussion

Here we provide a guide for how to perform Y2H assays in batch using optimized methods. There are a few critical steps in the procedure to help ensure that the population of yeast that would be placed under selection is representative of the starting library and that enough of the starting yeast population is used to undergo selection to limit variability. Importantly, these benchmarks are relatively easy to achieve alongside adapting the methods and materials for a traditional Y2H assay, thus making this approach access.......

Access restricted. Please log in or start a trial to view this content.

Disclosures

The authors have nothing to disclose

Acknowledgements

We thank the staff within the Institute of Human Genetics for NGS library preparation and sequencing. We thank Einat Snir for her expertise in preparing genomic library fragments for the Y2H plasmid library made here. This work was supported by National Institutes of Health: NIH R21 EB021870-01A1 and by NSF Research Project Grant: 1517110.

....

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Illumina HiSeq 4000Illuminadeep sequencing platform
Monoclonal anti-HA antibodiesBiolegend901514Primary Antibody to detect expression of HA in pGal4AD constructs
Polyclonal anti-myc antibodiesQED Biosciences Inc18826Primary Antibody to detect expression of MYC in pTEF-GBD constructs
NarINew England BioLabsR0191S
EcoRI-HFNew England BioLabsR3101S
BamHI-HFNew England BioLabsR3236S
XhoINew England BioLabsR0146S
Polyethylene Glycol 3350, powderJ.T. BakerU2211-08
Salmon Sperm DNATrevigen, Inc sold by Fisher Scientific50-948-286carrier DNA for yeast transformation section 3.2.1.
Kanamycin MonosulfateResearch Products InternationalK22000
LE AgaroseGeneMateE-3120-500used for making DNA agarose gels
Sodium ChlorideResearch Products InternationalS23025
TryptoneResearch Products InternationalT60060
D-SorbitolResearch Products InternationalS23080
Lithium Acetate DihydrateMP Biomedicals155256
Calcium ChlorideThermoFisherC79
EDTA Sodium SaltResearch Products InternationalE57020
Yeast Extract PowderResearch Products InternationalY20020
Yeast Nitrogen Base (ammonium sulfate) w/o amino acidsResearch Products InternationalY20040
CSM-Trp-Leu+40ADEFormediumDCS0789
CSM-Trp-Leu-His+40ADEFormediumDCS1169
CSM-Leu-MetFormediumDCS0549
CSM-Trp-MetBio 101, Inc4520-922
L-MethionineFormediumDOC0168
AdenineResearch Products InternationalA11500
D-(+)-GlucoseResearch Products InternationalG32045
Bacto AgarBD214010used for making media plates in section 1
PeptoneResearch Products InternationalP20240
3-amino-1,2,4 TriazoleSigmaA8056
2-Mercaptoehanol (BME)Sigma-AldrichM6250
Zymolyase 100TUSBiologicalZ1004
Potassium phosphate dibasicSigmaP8281
Phenol:Chloroform:IAAAmbionAM9732
Ammonium AcetateSigma-Aldrich238074
EthanolDecon Laboratories, INC2716
RNAse AThermoFisherEN0531
UreaResearch Products InternationalU20200
SDSResearch Products InternationalL22010
glycerolSigma AldrichG5516
Tris-HClGibco15506-017
bromophenol blueAmresco449
Gibson Assembly Cloning KitNew England BiolabsE5510SRapid assembly method for cloning of plasmids in section 2
NEBNext High-Fidelity 2x PCR Master MixNew England BiolabsM0541SUsed for amplification of products for Gibson Assembly in Section 2.3 as well assample preparation for DEEPN deep sequencing in section 6.2.1
Ethidium BromideAmresco0492-5G
QIAquick PCR purification kitQiagen28104Used for purification of pcr products in section 6.2.3
Qiaquick DNA Gel Extraction KitQiagen28704Used for purification of digested pTEF-GBD in section 2.1
KAPA Hyper Prep kitKAPA BiosystemsKK8500preparation kit for deep sequencing
Codon optimizationhttp://www.jcat.de
Codon optimizationhttps://www.idtdna.com/CodonOpt
gBlocksIntegrated DNA TechnologiesDNA fragments used for cloning in Section 2.2
StringsThermofisherDNA fragments used for cloning in Section 2.2
GenCatch Plasmid DNA mini-prep KitEPOCH Life SciencesUsed to prepare quantities of DNA in Section 2.3
Covaris E220Covarishigh performance ultra-sonicator in section 7
oligo nucelotide 5’- CGGTCTT
CAATTTCTCAAGTTTCAG -3’
Integrated DNA Technologies or Thermofisherused for pcr amplification and sequencing 5' insert pTEF-GBD during plasmid construction
oligo nucelotide 5’-GAGTAACG
ACATTCCCAGTTGTTC-3’
Integrated DNA Technologies or Thermofisherused for pcr amplification and sequencing 5' insert pTEF-GBD during plasmid construction
oligo nucelotide 5’-CACCGTAT
TTCTGCCACCTCTTCC-3’
Integrated DNA Technologies or Thermofisherused for pcr amplification and sequencing 3' insert pTEF-GBD during plasmid construction
oligo nucelotide 5’-GCAACCGC
ACTATTTGGAGCGCTG-3’
Integrated DNA Technologies or Thermofisherused for pcr amplification and sequencing 3' insert pTEF-GBD during plasmid construction
oligonucleotide 5’-GTTCCGATG
CCTCTGCGAGTG-3’
Integrated DNA Technologies or Thermofisher5' Pimer used for insert amplification of pGAL4AD
oligonucelotide 5’-GCACATGCT
AGCGTCAAATACC-3’
Integrated DNA Technologies or Thermofisher3' Pimer used for insert amplification of pGAL4AD
oligonucelotide 5’-ACCCAAGCA
GTGGTATCAACG-3’
Integrated DNA Technologies or Thermofisher5' Pimer used for insert amplification of pGADT7
oligonucelotide 5’- TATTTAGA
AGTGTCAACAACGTA -3’
Integrated DNA Technologies or Thermofisher3' Pimer used for insert amplification of pGADT7
PJ69-4A MatA yeast strainhttp://depts.washington.edu/yeastrc/ James P, Halladay J, Craig EA: Genomic Libraries and a host strain designed for highly efficient two-hybrid selection in yeast. GENETICS 1996 144:1425-1436MATA leu2-3,112 ura3-52 trp1-901 his3-200 gal4D, gal80D, GAL-ADE2 lys2::GAL1-HIS3 met2::GAL7
pTEF-GBDDr. Robert Piper LabGal4-DNA binding doimain expression plasmid
pGal4AD (pPL6343)Dr. Robert Piper LabGal4-activation domain expression plasmid
100 mm petri dishesKord-Vallmark sold by VWR2900
125 mL PYREX Erlenmeyer flaskFisher ScientificS63270
250 mL PYREX Erlenmeyer flaskFisher ScientificS63271
1,000 mL PYREX Erlenmeyer flaskFisher ScientificS63274
2,000 mL PYREX Erlenmeyer flaskFisher ScientificS63275
20 X 150 mm Disposable Culture TubeThermofisher14-961-33
pipet-aidDrummond4-000-100
5 mL Serological PipetteDenvilleP7127
10 mL Serological PipetteDenvilleP7128
25 mL Serological PipetteDenvilleP7129
1,000 mL PYREX Griffin BeakerFisher Scientific02-540P
1,000 mL PYREX Reuasable Media Storage BottleFisher Scientific06-414-1D
1,000 mL graduated cylinderFisher Scientific08-572-6G
SpectraMax 190Molecular Devicesused to measure the Optical Density of cells
NanoDrop 2000Thermo ScientificND-2000Spectrophotometer used to quantify amount of DNA
Electronic UV transilluminatorUltra LumMEB 20used to visualize DNA in an Ethidium Bromide agarose gel
P1000 Gilson PIPETMANFisher ScientificF123602G
P200 Gilson PIPETMANFisher ScientificF123601G
P20 Gilson PIPETMANFisher ScientificF123600G
P10 Gilson PIPETMANFisher ScientificF144802G
1250 µL Low Retention Pipette TipsGeneMateP-1236-1250
200 µLLow Retention Pipette TipsVWR10017-044
10 µL XL Low Retention Pipette TipsVWR10017-042
50 mL conical tubeVWR490001-627
15 mL conical tubeVWR490001-621
cell scraperDenville ScientificTC9310
1.5 mL Microcentrifuge tubesUSA Scientific1615-5500
HClFluka Analytical318949-1L
NaOHJ.T. Baker5674-02
Wooden applicatorsSolon Care55900
Eppendorf microcentrifuge 5424Fisher Scientific05-400-005microcentrifuge
Sorvall ST16RThermo Fisher Scientific75004381benchtop centrifuge
Amersham ECL Rabbit IgG, HRP-linked whole Ab (from donkey)GE HealthcareNA934-1MLSecondary Antibody
Amersham ECL Mouse IgG, HRP-linked whole Ab (from sheep)GE HealthcareNA931-1MLSecondary Antibody
SuperSignal West Pico Chemiluminescent SubstrateThermo Fisher Scientific34080ECL detection solution
Isotemp IncubatorThermo Fisher ScientificIncubator
Mutitron 2INFORS HTShaking incubator
Isotemp Digital-Control Water Bath Model 205Fisher Scientificwater bath
Y2H mouse cDNA library in Y187 (pan tissue)Clontech630482commercially available cDNA Library
Y2H mouse cDNA library in Y187 (mouse brain)Clontech630488commercially available cDNA Library
pGADT7 AD VectorClontech630442commercially available AD Vector housing many cDNA libraries
pGBKT7 DNA-BD VectorClontech630443commercially available DNA-BD Vector
Biolase DNA PolymeraseBiolineBIO-21042DNA polymerase used for section 2.4
GeneMate GCL-60 Thermal CyclerBioExpressP-6050-60pcr machine
TempAssure 0.5 mL PCR tubesUSA Scientific1405-8100

References

  1. Fields, S., Song, O. A novel genetic system to detect protein-protein interactions. Nature. 340 (6230), 245-246 (1989).
  2. Bruckner, A., Polge, C., Lentze, N., Auerbach, D., Schlattner, U. Yeast two-hybrid, a powerful tool for systems biology. International Journal of Mo....

Access restricted. Please log in or start a trial to view this content.

Reprints and Permissions

Explore More Articles

Protein-Protein InteractionsDEEPN MethodDeep SequencingBait Plasmid ConstructionPrey Library PreparationYeast Mating ReactionsDNA Extraction ProtocolPCR AmplificationBioinformatics Processing