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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This article provides a straightforward and clear protocol to label Salmonella secreted effectors using genetic code expansion (GCE) site-specifically and image the subcellular localization of secreted proteins in HeLa cells using direct stochastic optical reconstruction microscopy (dSTORM)

Abstract

Type three secretion systems (T3SSs) enable gram-negative bacteria to inject a battery of effector proteins directly into the cytosol of eukaryotic host cells. Upon entry, the injected effector proteins cooperatively modulate eukaryotic signaling pathways and reprogram cellular functions, enabling bacterial entry and survival. Monitoring and localizing these secreted effector proteins in the context of infections provides a footprint for defining the dynamic interface of host-pathogen interactions. However, labeling and imaging bacterial proteins in host cells without disrupting their structure/function is technically challenging.

Constructing fluorescent fusion proteins does not resolve this problem, because the fusion proteins jam the secretory apparatus and thus are not secreted. To overcome these obstacles, we recently employed a method for site-specific fluorescent labeling of bacterial secreted effectors, as well as other difficult-to-label proteins, using genetic code expansion (GCE). This paper provides a complete step-by-step protocol to label Salmonella secreted effectors using GCE site-specifically, followed by directions for imaging the subcellular localization of secreted proteins in HeLa cells using direct stochastic optical reconstruction microscopy (dSTORM)

Recent findings suggest that the incorporation of non-canonical amino acids (ncAAs) via GCE, followed by bio-orthogonal labeling with tetrazine-containing dyes, is a viable technique for selective labeling and visualization of bacterial secreted proteins and subsequent image analysis in the host. The goal of this article is to provide a straightforward and clear protocol that can be employed by investigators interested in conducting super-resolution imaging using GCE to study various biological processes in bacteria and viruses, as well as host-pathogen interactions.

Introduction

Bacterial infections have long been regarded as a serious hazard to human health. Pathogens use highly evolved, extremely powerful, and intricate defense systems, as well as a variety of bacterial virulence factors (referred to as effector proteins) to evade host immune responses and establish infections1,2. However, the molecular mechanisms underlying these systems and the role of individual effector proteins are still largely unknown due to the dearth of suitable approaches for directly following the crucial protein components and effectors in host cells during pathogenesis.

One t....

Protocol

1. Plasmid construction

  1. Clone the gene expressing the POI into an expression plasmid (e.g., pET28a-sseJ10TAG) that expresses the POI in E. coli BL21 (DE3). This step facilitates in determining that the mutants are functional. 
  2. For the visualization of Salmonella secreted effectors in host cells, construct an expression plasmid (pWSK29-sseJ-HA) that expresses the target POI SseJ under the control of its native promoter, as described in previous reports7,12,24. Using site-directed mutagenesis, repla....

Results

This protocol paper describes a GCE-based method for site-specific fluorescent labeling and visualization of Salmonella secreted effectors, as depicted in Figure 1. Chemical structure of the ncAA bearing trans-cyclooctene bioorthogonal group (TCO) and the fluorescent dye are shown in Figure 1A. SseJ labeling was achieved by genetic incorporation of bioorthogonal ncAAs at an amber stop codon (see Figu.......

Discussion

The approach described herein was used to track the precise location of effector proteins injected into the host cell by the bacterial T3SS after infection. T3SSs are employed by intracellular pathogens such as Salmonella, Shigella, and Yersinia to transport virulence components into the host. The development of super-resolution imaging technologies has made it possible to visualize virulence factors at a previously unimaginable resolution12,.......

Disclosures

The authors declare that they have no competing financial interests.

Acknowledgements

This work was supported by start-up funds from the University of Texas Medical branch, Galveston, TX, and a Texas STAR award to L.J.K. We thank Prof. Edward Lemke (European Molecular Biology Laboratory, Heidelberg, Germany) for plasmid pEVOL-PylRS-AF. Images in Figure 1 were created using BioRender.

....

Materials

NameCompanyCatalog NumberComments
10x Tris/Glycine SDS running bufferBIO-RAD1610732
Ammonium chlorideFischer ScientificA661-500
Ammonium sulphateFischer ScientificBP212R-1
Ampicillin SodiumSigma-AldrichA01665 g
Antibiotic-Antimycotic (100x)ThermiFischer Scientific15240096
ArabinoseSigma-AldrichA3256500 g
Avanti J-26XP (High-Performance Centrifuge)Beckman Coulter
Bacto-AgarBD Diagnostics, Franklin Lakes, USA214010
BDP-FL-tetrazineLumiprobe (USA)2.14E+02
β-mercaptoethanolMillipore444203250 mL
Bromophenol blueSigma-AldrichB8026
BSASigma-AldrichA4503500 g
CaseinSigma-AldrichC8654
CatalaseSigma-AldrichC9322
ChloramphenicolSigma-AldrichC1919
Click Amino Acid / trans-Cyclooct-2-en – L - Lysine (TCO*A)SiChem GmbHSC-8008Size: 500 mg
DAPI (Hoechst33342)InvitrogenH3570
DeNovix DS-11+ SpectrophotometerDeNovix
DMEM*Corning10-013-CV* Used for maintaining HeLa Cell
DMEM**Gibco11965-092**Used for bacterial infection in presence of ncAA, see section 5.4.
DMSOSigma-AldrichD8418250 g
Donkey anti-rabbit Alexa fluoro555 secondary antibodyInvitrogenA-31572
DPBS, 1xCorning21-031-CV
E. coli strain BL21 (DE3)Novagen (Madison, WI)
EMCCD CameraAndoriXon Ultra 897-BV
Eppendorf Safe-Lock Tube 1.5 mL (PCR clean)Eppendorf, Hamburg, Germany30123.328
Fetal Bovine Serum (FBS)Fischer10082147
Fisherbrand Syringe Filters - Sterile (PVDF 0.22 µm)Fischer Scientific97203Pack of 100
Gene Pulser Xcell ElectroporatorBIO-RAD1652660
GentamycinSigma-AldrichG127210 mL
Gibco L-Glutamine (200 mM), 100xFischer Scientific25-030-081
Glucose oxidaseSigma-AldrichG7141-50KU
GlycerolFischer ScientificBF229-4
HeLa cellsATTCCCL-2
HEPES BufferCorning25-060-C1100 mL
Hydrocloric acidFischer ScientificA144-212
ImageJImage processing and analysis:  http://rsbweb.nih.gov/ij
IntantBlueExpedeonISB1LCoomassie-based stain
Isopropyl β-D-1-thiogalactopyranoside (IPTG)Sigma-AldrichI5502
Janelia Fluoro 646-tetrazineTocris Bioscience7279
KanamycinSigma-Aldrich606155 g
LB BrothBD Difco244620500 g
LysozymeSigma-AldrichL6876
μManager (v. 1.4.2)https://micro-manager.org/Download_Micro-Manager_Latest_Release
MESSigma-AldrichM3671250 g
Micro pulser cuvetteBIO-RAD165-20860.2 cm electrode gap, pkg. of 50
Nikon N-STORMNikon Instruments Inc.https://www.microscope.healthcare.nikon.com/products/super-resolution-microscopes/n-storm-super-resolution
Nunc EasYFlask Cell Culture FlasksThermiFischer Scientific156499
Omnipur Casamino AcidCalbiochem2240500 g
Paraformaldehhyde (PFA)Electron Microscopy Sciences 15710
PBS (10x)Roche11666789001
Penicillin-Streptomycin Solution (100x)GenDEPOT CA005-010100 mL
pEVOL-PylRS-AFFor plasmid construction and map see following references
1. Angew Chem Int Ed Engl. 2011, 50(17), 3878-81.
2. Angew Chem Int Ed Engl., 2012, 51, 4166-70.
Plasmid Mini-prep KitQiagen27106
plasmid pWSK29-sseJ10TAG-HARef.: elife. 2021, 10, e67789.
plasmid pWSK29-sseJ-HARef.: elife. 2021, 10, e67789.                                                                   Vector map of PWSK29: https://www.addgene.org/172972/
Pluronic F-127Millipore540025Protein grade, 10% Solution
Potassium phosphate monobasicFischer ScientificP285-500
Potassium sulphateAcros Organic424220250
Protease Inhibitor Cocktail Set I - CalbiochemSigma-Aldrich539131100x Solution
Rabbit anti-HA primary antibodySigma-AldrichH6908
S. enterica. serovar Typhimurium 14028sRef.: PLoS Biol. 2015, 13, e1002116.
SaponinSigma-Aldrich47036-50G-F
Sodium dodecyl sulfate (SDS)Sigma-AldrichL3771
Sodium hydroxideFischer ScientificSS255-1
Sodium Pyruvate (100 mM), 100xCorning25-060-C1100 mL
Sonic Dismembrator Model 100Fischer Scientific24932
STED microsocpe (Leica TCS SP8 STED 3X system)Leica Microsystems, Wetzlar, Germanyhttps://www.leica-microsystems.com/products/confocal-microscopes/p/leica-tcs-sp8-sted-one/
ThunderSTORMhttps://zitmen.github.io/thunderstorm/
Trizma BaseSigma-AldrichT1503
Trypsin-EDTA (1x), 0.25%  GenDEPOT CA014-010
Tween-20Sigma-AldrichP9416100 mL
X-well tissue culture chamber slidesSARSTEDT94.6190.802

References

  1. Marlovits, T. C., et al. Structural insights into the assembly of the type III secretion needle complex. Science. 306 (5698), 1040-1042 (2004).
  2. Kubori, T., et al. Supramolecular structu....

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