Escherichia coli -Based Complementation Assay to Study the Chaperone Function of Heat Shock Protein 70

Summary

This protocol demonstrates the chaperone activity of heat shock protein 70 (Hsp70). E. coli dnaK756 cells serve as a model for the assay as they harbor a native, functionally impaired Hsp70, making them susceptible to heat stress. The heterologous introduction of functional Hsp70 rescues the growth deficiency of the cells.

Abstract

Heat shock protein 70 (Hsp70) is a conserved protein that facilitates the folding of other proteins within the cell, making it a molecular chaperone. While Hsp70 is not essential for E. coli cells growing under normal conditions, this chaperone becomes indispensable for growth at elevated temperatures. Since Hsp70 is highly conserved, one way to study the chaperone function of Hsp70 genes from various species is to heterologously express them in E. coli strains that are either deficient in Hsp70 or express a native Hsp70 that is functionally compromised. E. coli dnaK756 cells are unable to support λ bacteriophage DNA. Furthermore, their native Hsp70 (DnaK) exhibits elevated ATPase activity while demonstrating reduced affinity for GrpE (Hsp70 nucleotide exchange factor). As a result, E. coli dnaK756 cells grow adequately at temperatures ranging from 30 °C to 37 °C, but they die at elevated temperatures (>40 °C). For this reason, these cells serve as a model for studying the chaperone activity of Hsp70. Here, we describe a detailed protocol for the application of these cells to conduct a complementation assay, enabling the study of the in cellulo chaperone function of Hsp70.

Introduction

Heat shock proteins play an important role as molecular chaperones by facilitating protein folding, preventing protein aggregation, and reversing protein misfolding^1,2. Heat shock protein 70 (Hsp70) is one of the most prominent molecular chaperones, playing a central role in protein homeostasis^3,4. DnaK is the E. coli Hsp70 homologue⁵.

Various biophysical, biochemical, and cell-based assays have been developed to explore the chaperone activity of Hsp70 and to screen for inhibitors targeting this chaperone^6,7,8. Hsp70 is a highly conserved protein. For this reason, several Hsp70s of eukaryotic organisms, such as Plasmodium falciparum (the main agent of malaria), have been reported to substitute for DnaK function in E. coli^6,9. In this way, an E. coli-based complementation assay has been developed involving the heterologous expression of Hsp70s in E. coli to explore their cytoprotective function. Typically, this assay involves the utilization of E. coli cells that are either deficient for DnaK or that express a native DnaK that is functionally compromised. While DnaK is not essential for E. coli growth under normal conditions, it becomes essential when the cells are grown under stressful conditions such as elevated temperatures or other forms of stress^10,11.

E. coli strains that have been developed to study Hsp70 function using a complementation assay include E. coli dnaK103 (BB2393 [C600 dnaK103(Am) thr::Tn10]) and E. coli dnaK756. E. coli dnaK103 cells produce a truncated DnaK that is non-functional, and as such, the cells grow adequately at 30 °C, while the strain is sensitive to cold and heat stress^12,13. Similarly, the E. coli dnaK756/BB2362 (dnaK756 recA::TcR Pdm1,1) strain does not grow above 40 °C^14,15. The E. coli dnaK756 strain expresses a mutant native DnaK (DnaK756) characterized by three glycine-to-aspartate substitutions at positions 32, 455, and 468, giving rise to compromised proteostatic outcomes. Consequently, this strain is resistant to bacteriophage λ DNA¹⁴. Additionally, E. coli dnaK756 exhibits elevated ATPase activity, while its affinity for the nucleotide exchange factor, GrpE, is reduced¹⁶. E. coli DnaK mutant strains serve as ideal models for investigating the chaperone activity of Hsp70 through a complementation approach. Since DnaK is only essential under stressful conditions, the complementation assay is typically conducted at elevated temperatures (Figure 1). Some advantages of using E. coli for this study include its well-characterized genome, rapid growth, and the low cost of culturing and maintenance¹⁷.

In this article, we describe in detail a protocol involving the use of E. coli dnaK756 cells to study the function of Hsp70. The Hsp70s we employed in the assay are wild-type DnaK and its chimeric derivative, KPf (made up of the ATPase domain of DnaK fused to the C-terminal substrate-binding domain of Plasmodium falciparum Hsp70-1^6,18). KPf-V436F was heterologously expressed as a negative control since the mutation essentially blocks it from binding substrates, thus abrogating its chaperone activity⁹.

Protocol

1. Transformation

NOTE: Use sterile glassware for culture, pipette tips, and freshly prepared and autoclaved media. Prepare cultures of the E. coli cells in 2x yeast tryptone (YT) [1.6% tryptone (w/v), 1% yeast extract (w/v), 0.5% NaCl (w/v), 1.5% agar (w/v)] agar. General reagents used in the protocol and their sources are provided in the Table of Materials.

1. Label 2.0 mL microcentrifuge tubes and aliquot 50 µL of competent E. coli dnaK756cells, keeping the cells on ice.
2. To the 2.0 mL microcentrifuge tubes with competent cells, aliquot 10-50 ng of pQE60/DnaK, pQE60/KPf, and pQE60/KPf-V436F plasmid DNA⁹ into separate tubes.
3. Keep the 2.0 mL microcentrifuge tubes containing the competent cells and plasmid DNA on ice for 30 min.
4. Heat shock the competent cells-DNA mix for 60 s at 42 °C and return the microcentrifuge tubes back on ice for 10 min.
5. Add 950 µL of fresh 2x YT broth (pre-incubated at 37 °C) and incubate at 37 °C while shaking at 150 revolutions/min for 1 h. Leave the cells to grow for much longer to encourage their recovery if necessary.
   NOTE: Avoid shaking the cells vigorously.
6. Pipette 100 µL of the cells and spread them onto 2x YT agar plates containing 50 µg/mL kanamycin, 10 µg/mL tetracycline for the respective strain, and 100 µg/mL ampicillin (see Table of Materials) for plasmid selection.
7. Centrifuge the rest of the cells (whose volume is now approximately 900 µL) for 1 min at 5000 x g (at 4 °C) using a benchtop microcentrifuge.
8. Decant about 800 µL of the broth and use the remaining medium to resuspend the pelleted cells.
9. Plate the recovered cells onto the 2x YT agar plate.
10. Incubate both agar plates overnight (or approximately 17 h) at 37 °C.
    NOTE: These cells grow very slowly and may need to be incubated for much longer. Be careful to spot the colonies which may start off very small. The plate containing cells resuspended after centrifugation (step 1.7) serves as a back-up in case the transformation efficiency of the cells is poor, in which case the pelleted cells may improve the recovery of any transformed cells. However, if the transformation efficiency is excellent, the agar plate onto which concentrated cells were plated may be characterized by an overgrown culture upon incubation, making it difficult to identify single colonies. In that case, the other agar plate may be the one on which well-spaced colonies grow.

2. Cell plating

1. Pick up a single colony from the transformants and inoculate it into 10 mL of 2x YT broth supplemented with 50 µg/mL of kanamycin, 10 µg/mL of tetracycline for the selection of the E. coli dnaK756 cells, and 100 µg/mL ampicillin for plasmid selection.
   NOTE: Use flasks (≥50 mL) to ensure aeration when agitating the culture. Incubate the inoculum overnight (17 h) at 37 °C while shaking at 150 rotations/min.
2. Take an absorbance reading at OD₆₀₀ the following morning.
3. Clean the workbench surface using 75% ethanol to swab the surface in preparation for cell spotting.
4. Using a 2 mL microcentrifuge tube, standardize the culture to an OD₆₀₀ reading of 2.0 using 2x YT broth.
   NOTE: Ensure that the OD readings are taken correctly as this step is important for standardizing cell density across the various samples.
5. Using 2 mL microcentrifuge tubes, prepare serial dilutions of the cells from 10⁰ to 10^-5.
6. Incubate the agar plates to be used to spot the cells onto in an oven set at 40 °C to allow the plates to dry with lids partially open to ensure water vapor escapes.
   NOTE: To ensure the cells are spotted at uniformly separated distances, draw lines on a piece of paper onto which a template of spotting sites is printed.
7. Spot 2 µL of the serially diluted cells onto the agar plates supplemented with 50 µg/mL kanamycin, 10 µg/mL tetracycline, 100 µg/mL ampicillin, and 0.5 mM IPTG (for the induction of expression of the recombinant proteins) (see Table of Materials).
8. Spot each sample onto two separate plates (one to be incubated at 37 °C and the other at 43.5 °C).
   NOTE: Avoid piercing the agar plate.
9. Spot control samples onto the same plate as the experimental samples to minimize environmental effects.
10. Conduct the spotting quickly to ensure the process is completed before the cells start growing, as this may generate skewed growth patterns.
    NOTE: It is important to avoid aerosols when spotting, as these would contaminate the plates. It is also important to keep the plates closed in between the spotting to avoid contamination.
11. Incubate one plate at 37 °C (permissive growth temperature) and the other at the non-permissive growth temperature of 43.5 °C.
    NOTE: Incubate the plates facing upside down to avoid steam collecting onto the lid, as the condensed water would wash the spotted colonies off their positions.
12. Place all the plates in the incubators at the same time and avoid opening the incubator until the following morning.
    NOTE: Opening the incubator door several times during incubation of the plates is discouraged. This is because the access of air into the incubator may result in temperature fluctuations that adversely impact cell growth.

3. Confirming expression of recombinant proteins

1. Using a sterile loop, pick up part of the remaining cells from the same colony of transformed E. coli dnaK756 cells.
2. Inoculate the cells into 10 mL YT broth supplemented with 50 µg/mL kanamycin, 10 µg/mL tetracycline, and 100 µg/mL ampicillin. Incubate overnight (17 h) at 37 °C while shaking at 150 revolutions/min.
3. Transfer the culture into 90 mL of sterile 2x YT broth containing the necessary antibiotics as mentioned in step 3.2. Let the cells grow to mid-log phase (OD₆₀₀ = 0.4-0.6).
4. Take 2 mL of the sample culture before induction (0 h induction sample).
5. Add IPTG to a final concentration of 1 mM to induce protein production and re-incubate the cells at 37 °C.
6. Take a second 2 mL sample 6 h post-induction.
7. Harvest the cells by centrifuging at 5000 x g for 10 min. Keep the centrifuge temperature at 4 °C.
8. Discard the supernatant.
9. Resuspend the pellet in PBS buffer (137 mM NaCl, 27 mM KCl, 4.3 mM Na₂HPO₄, 1.4 mM KH₂PO₄) and store at -20 °C.

4. SDS-PAGE and western blot analyses

1. Prepare 2x 10% SDS gels as previously described¹⁹.
2. Keep one of the SDS-PAGE gels for subsequent staining using Coomassie stain to view the protein bands. Use the second SDS-PAGE gel to conduct western blot analysis.
3. Aliquot 80 µL of the resuspended samples and mix it with 20 µL of 4x Laemmli SDS loading buffer.
4. Boil the suspension at 100 °C for 10 min. Then load 10 µL of each sample onto the precast SDS gel (see Table of Materials).
5. Perform electrophoresis at room temperature for 1 h using a voltage of 120 V in a 1x solution of SDS running buffer (25 mm Tris, 250 mm glycine, 0.1% (w/v) SDS).
6. Stain the gel with Coomassie stain (see Table of Materials) for 1 h, followed by destaining using destaining buffer (50% (v/v) methanol, 10% (v/v) acetic acid in distilled water) for 2 h.
7. Visualize the protein bands present in the gel using a gel imaging system (see Table of Materials). Rerun another SDS-PAGE gel with the same samples following the above-mentioned protocol.
8. When the electrophoretic run ends, take SDS-PAGE gels to conduct western blot analysis as previously described¹⁹.
9. Wash the nitrocellulose membrane onto which the proteins were transferred three times in wash buffer (TBS-Tween, pH 7.4 [50 mM Tris, 150 mM NaCl, 1% (v/v) Tween]).
10. Use α-DnaK (see Table of Materials) to detect DnaK and α-PfHsp70-1⁷ to detect KPf and its mutant, KPf-V436F), respectively.
11. Use the antibodies at a 1:2000 dilution in 5% non-fat milk. Incubate at 4 °C while shaking at 60 revolutions/min for 1 h.
12. Remove non-specifically bound antibody by washing the nitrocellulose membrane in TBS-Tween 3 times in 15 min.
13. Incubate the membrane in the secondary antibody (α-rabbit, see Table of Materials) under the same conditions as the previous step. This is followed by subsequent washing under the same conditions as the primary antibody.
14. Resolve the bands using enhanced chemiluminescence (ECL) detection reagent.
15. Visualize the bands using a gel imager.

Results

Figure 2 presents an image of the scanned agar containing cells that were spotted and cultured at the permissive growth temperature of 37 °C and 43.5 °C, respectively. On the right-hand side of Figure 2, excised western blot components represent the expression of DnaK, KPf, and KPf-V436F in E. coli dnaK756 cells. As expected, all the E. coli dnaK756 cells cultured at the permissive growth temperature of 37 °C manag...

Discussion

The protocol demonstrates the utility of E. coli dnaK756cells in exploring the chaperone function of heterologously expressed Hsp70. This assay could be adopted to screen inhibitors targeting Hsp70 function in cellulo. However, one limitation of this method is that Hsp70s unable to substitute for DnaK in E. coli are not compatible with this assay. Lack of post-translational modification²¹ of some non-native Hsp70s may account for their lack of function within the

Materials

Name	Company	Catalog Number	Comments
2-β-Mercaptoethanol	Sigma-Aldrich	8,05,740	Constituent for sample loading dye
Acetic acid	Labchem	101005125	Constituent of destainer
Acrylamide	Sigma-Aldrich	8008300100	Component of SDS
Agar	Merck	HG000BX1.500	Constituent of medium and liquid growth assay
Agarose	Clever Scientific	14131031	Certified molecular biology agarose
Ammonium persulfate	Sigma-Aldrich	101875295	Constituent for SDS-PAGE gel
Ampicillin	VWR International	0339—EU—25G	Selective antibiotic
Bis	Sigma-aldrich	1015460100	Component of SDS
Bromophenol	Sigma-Aldrich	0449-25G	Constituent for sample loading dye
CaCl2	Sigma-Aldrich	10043-52-4	For competent cells preparation
Coomassie brilliant blue	VWR International	443293X	SDS-PAGE dye
Dibasic sodium phosphate	Sigma-Aldrich	RB10368	Constituent of PBS buffer
ECL	Thermofischer Scientific	32109	Western blot detection reagent
Ethidium Bromide	Thermofischer Scientific	17898	DNA intercalating dye
Glycerol	Merck	SAAR2676520L	Constituent for sample loading dye
Glycine	VWR International	10119CU	Component of SDS
IPTG	Glentham life sciences	162IL	inducer
Kanamycin	Melford	K0126	Selective antibiotic
Magnesium Chloride	Merck	SAAR4123000EM	Constituent of medium and liquid growth assay
Methanol	Labchem	113140129	Constituent of destainer
Monobasic potassium phosphate	Merck	1,04,87,30,250	Constituent of PBS buffer
Peptone	Merck	HG000BX4.250	Constituent of medium and liquid growth assay
Potassium chloride	Merck	SAAR5042020EM	Constituent of PBS buffer
PVDF membrane	Thermofischer scientific	PB7320	Western blot membrane
Sodium Chloride	Merck	SAAR5822320EM	Constituent of medium and liquid growth assay
Sodium dodecyl sulphate	VWR International	108073	To resolve expressed proteins
Spectramax iD3	Separations	373705019	Automated plate reader
TEMED	VWR international	ACRO420580500	Component of SDS gel
Tetracycline	Duchefa Biochemies	T0150.0025	Selective antibiotic
Tris	VWR International	19A094101	Component of SDS gel
Tween20	Merck	SAAR3164500XF	Constituent for Western wash buffer
Western transfer chamber	Thermofisher Scientific	PB0112	Transfer of protein to nitrocellulose membrane
Yeast extract	Merck	HG000BX6.500	Constituent of medium and liquid growth assay
α-DnaK antibody	Inqaba	BK CAC09317	Primary antibody
α-rabbit antibody	Thermofischer scientific	31460	Secondary antibody