In Situ Monitoring of Transiently Formed Molecular Chaperone Assemblies in Bacteria, Yeast, and Human Cells

Summary

Cognate J-domain proteins cooperate with the Hsp70 chaperone to assist in a myriad of biological processes ranging from protein folding to degradation. Here, we describe an in situ proximity ligation assay, which allows the monitoring of these transiently formed chaperone machineries in bacterial, yeast and human cells.

Abstract

J-domain proteins (JDPs) form the largest and the most diverse co-chaperone family in eukaryotic cells. Recent findings show that specific members of the JDP family could form transient heterocomplexes in eukaryotes to fine-tune substrate selection for the 70 kDa heat shock protein (Hsp70) chaperone-based protein disaggregases. The JDP complexes target acute/chronic stress induced aggregated proteins and presumably help assemble the disaggregases by recruiting multiple Hsp70s to the surface of protein aggregates. The extent of the protein quality control (PQC) network formed by these physically interacting JDPs remains largely uncharacterized in vivo. Here, we describe a microscopy-based in situ protein interaction assay named the proximity ligation assay (PLA), which is able to robustly capture these transiently formed chaperone complexes in distinct cellular compartments of eukaryotic cells. Our work expands the employment of PLA from human cells to yeast (Saccharomyces cerevisiae) and bacteria (Escherichia coli), thus rendering an important tool to monitor the dynamics of transiently formed protein assemblies in both prokaryotic and eukaryotic cells.

Introduction

A vast amount of genomic information remains uninterpretable due to our incomplete understanding of cellular interactomes. Conventional protein-protein interaction detection methodologies such as protein co-immunoprecipitation with/without chemical cross-linking and protein co-localization, though widely used, pose a range of disadvantages. Some  of the main disadvantages include poor quantification of the interactions and the potential introduction of non-native binding events. In comparison, emerging proximity-based techniques provide an alternative and a powerful approach for capturing protein interactions in cells. The proximity ligation assay (PLA)¹, now available as a proprietary kit, employs antibodies to specifically target protein complexes based on the proximity of the interacting subunits.

PLA is initiated by the  formation of a scaffold consisting of primary and secondary antibodies with small DNA tags (PLA probes) on the surface of the targeted protein complex (Figure 1, steps 1-3). Next, determined by the proximity of the DNA tags, a circular DNA molecule is generated via hybridization with connector oligonucleotides (Figure 1, step 4). The formation of the circular DNA is completed by a DNA ligation step. The newly formed circular piece of DNA serves as a template for the subsequent rolling circle amplification (RCA)-based polymerase chain reaction (PCR) primed by one of the conjugated oligonucleotide tags. This generates a single-stranded concatemeric DNA-molecule attached to the protein complex via the antibody scaffold (Figure 1, step 6). The concatemeric DNA molecule is visualized using fluorescently labeled oligonucleotides that hybridize to multiple unique sequences scattered across the amplified DNA (Figure 1, step 7)². The generated PLA signal, which appears as a fluorescent dot (Figure 1, step 7), corresponds to the location of the targeted protein complex in the cell. As a result, the assay could detect protein complexes with high spatial accuracy. The technique is not limited to simply capturing protein interactions, but could also be utilized to detect single molecules or protein modifications on proteins with high sensitivity^1,2.

Hsp70 forms a highly versatile chaperone system fundamentally important for maintaining cellular protein homeostasis by participating in an array of housekeeping and stress-associated functions. Housekeeping activities of the Hsp70 chaperone system include de novo protein folding, protein translocation across cellular membranes, assembly and disassembly of protein complexes, regulation of protein activity and linking different protein folding/quality control machineries³. The same chaperone system also refolds misfolded/unfolded proteins, prevents protein aggregation, promotes protein disaggregation and cooperates with cellular proteases to degrade terminally misfolded/damaged proteins to facilitate cellular repair after proteotoxic stresses^4,5. To achieve this functional diversity, the Hsp70 chaperone relies on partnering co-chaperones of the JDP family and nucleotide exchange factors (NEFs) that fine-tune the Hsp70’s ATP-dependent allosteric control of substrate binding and release^3,6. Further, the JDP co-chaperones play a vital role in selecting substrates for this versatile chaperone system. Members of this family are subdivided into three classes (A, B and C) based on their structural homology to the prototype JDP, the E. coli DnaJ. Class A JDPs contain an N-terminal J-domain, which interacts with Hsp70, a glycine-phenylalanine rich region, a substrate binding region consisting of a Zinc finger-like region (ZFLR) and two β-barrel domains, and a C-terminal dimerization domain. JDPs with an N-terminal J-domain and a glycine-phenylalanine rich region, but lacking the ZFLR, fall into class B. In general, members of these two classes are involved in chaperoning functions. Members falling under the catchall class C, which contains JDPs that only share the J-domain⁴, recruit Hsp70s to perform a variety of non-chaperoning functions. The important role of JDPs as interchangeable substrate recognition “adaptors” of the Hsp70 system is reflected by an expansion of the family members during evolution. For example, humans have over 42 distinct JDP members⁴. These JDPs function as monomers, homodimers and/or homo/hetero oligomers^4,5. Recently, a functional cooperation via transient complex formation between class A (e.g., H. sapiens DNAJA2; S. cerevisiae Ydj1) and class B (e.g., H. sapiens DNAJB1; S. cerevisiae Sis1) eukaryotic JDPs was reported to promote efficient recognition of amorphous protein aggregates in vitro^7,8. These mixed class JDP complexes presumably assemble on the surface of aggregated proteins to facilitate the formation of Hsp70- and Hsp70+Hsp100-based protein disaggregases^7,8,9,10. The critical evidence to support the existence of these transiently formed mixed class JDP complexes in eukaryotic cells was provided with PLA⁸.

PLA is increasingly employed for assessing protein interactions in metazoa, primarily in mammalian cells. Here, we report the successful expansion of this technique to monitor transiently formed chaperone complexes in eukaryotic and prokaryotic unicellular organisms such as the budding yeast S. cerevisiae and the bacterium E. coli. Importantly, this expansion highlights the potential use of PLA in detecting and analyzing microbes that infect human and animal cells.

Protocol

1. HeLa Cell Preparation

1. Prepare the following materials: PBS (137 mM NaCl, 2.7 mM KCl, 10 mM Na₂HPO₄, 1.8 mM KH₂PO₄), pH 7.4; DMEM, supplemented with 10% FCS and 1% Pen-Strep; 4% paraformaldehyde in PBS; 0.5% Triton-X100 in PBS; TBS-T (150 mM NaCl, 20 mM Tris, 0.05% Tween), pH 7.4; 0.0001% sterile poly-L-Lysine solution; 10-well diagnostic slides; a humid chamber; tissue paper; and Coplin slide-staining jars.
   NOTE: To ensure optimal fixation efficiency, paraformaldehyde solutions should be prepared fresh before every experiment.
2. Prepare a humid chamber by covering the bottom of a closed box with wet tissues. Place the humid chamber at 37 °C before starting the experiment, to ensure that the chamber temperature is at 37 °C while incubating the enzymatic reactions.
3. Culture HeLa cells in T25 flasks, in 5 mL of DMEM (High Glucose, Glutamate and Sodium Pyruvate supplemented) supplemented with 10% FCS and 1% Pen-Strep, in a 37 °C CO₂ incubator containing 5% CO₂. Dissociate adherent cells using 0.05% Trypsin-EDTA. After addition of fresh DMEM to dissociated cells, count cells using a cell counting chamber and grow on diagnostic slides inside a humid chamber.
4. Sterilize diagnostic slides by UV-irradiation in a sterile cell culture hood for 30 min.
5. Add 100 µL of sterile filtered 0.0001% poly-L-lysine to each well required for the experiment. Incubate for 30 min. Wash away excess poly-L-lysine by washing each well 3x with 50 µL ultrapure water.
6. Trypsinize the HeLa cells and add approximately 15,000 cells to each well. If necessary, dilute cells to at least 30-50 µL of DMEM per well.
7. Grow cells in a humid chamber within a 37 °C 5% CO₂ incubator for approximately 24 h. Cells should be 60%–80% confluent before commencing the PLA.
   NOTE: Too high a confluency decreases the absorption of reagents, decreasing the obtained signal at the end of the protocol.
8. Remove medium by placing a tissue paper at the edge of the well. Wash wells 3x with 50 µL of PBS.
   NOTE: Cells are subject to detaching when liquids are added harshly. This can be prevented by not letting the wells dry completely before adding new liquid and by adding the new liquid gently to the edge of the well.
9. Fix cells by adding 50 µL of freshly prepared 4% paraformaldehyde in PBS to each well. Incubate for 10 min at room temperature.
10. Wash slides 3x in PBS. Perform washes in a Coplin slide-staining jar containing 100 mL of PBS. For each wash, incubate for 5 min at room temperature without shaking.
11. Permeabilize the cell membrane by submerging the slides in 100 mL of 0.5% Triton-X100 in PBS in a Coplin slide-staining jar. Incubate for 10 min at room temperature without shaking.
12. Wash slides 3x in TBS-T. Perform washes in a Coplin slide-staining jar containing 100 mL of TBS-T. For each wash, incubate for 5 min at room temperature without shaking.
13. After the last wash, remove excess buffer with a tissue paper. At this point the cells are ready for the Proximity Ligation Assay protocol that will be discussed in section 4.

2. S. cerevisiae Cell Preparation

1. Prepare the following materials: 100 mM KPO₄, pH 6.5, referred to as Wash Buffer; 37% formaldehyde; 4% paraformaldehyde in 100 mM KPO₄, pH 6.5; 1.2 M sorbitol in 100 mM KPO₄, pH 6.5; lyticase solution (500 µg/mL lyticase, 20 mM β-mercaptoethanol, 100 mM KPO₄, pH 6.5); 0.0001% poly-L-Lysine solution; 1% Triton-X100 in 100 mM KPO₄, pH 6.5; 10-well diagnostic slides; a humid chamber (prepared as in step 1.2); tissue paper; and Coplin slide-staining jars.
   NOTE: To ensure optimal fixation efficiency, paraformaldehyde solutions should be prepared fresh before every experiment.
2. Grow an overnight culture in non-selective Yeast Extract, Peptone and Dextrose (YPD) medium at 30 °C while shaking.
   NOTE: Depending on experimental requirements S. cerevisiae cells can be grown in Synthetic Complete (SC) medium or selective Synthetic Minimal (SM) medium instead.
3. Dilute the stationary culture to an OD₆₀₀ of 0.1 in 20 mL medium. Grow the cells at 30 °C while shaking until the OD₆₀₀ reaches 0.5.
4. Transfer the 20 mL culture to a 50 mL centrifuge tube. Pellet the cells by centrifugation at 665 x g for 3 min. Remove the supernatant. Resuspend the cells in 5 mL of fresh medium.
5. Fix the cells by adding 550 µL of 37% formaldehyde to the culture. Incubate at room temperature for 15 min.
6. Pellet the cells by centrifugation at 665 x g for 3 min. Remove the supernatant. Resuspend the pellet in 1 mL of freshly prepared 4% paraformaldehyde in Wash Buffer. Incubate for 45 min at room temperature.
7. During the incubation, prepare the diagnostic slides by adding 100 µL of 0.01% poly-L-lysine solution to each well. Incubate the slides for 30 min at room temperature.
8. After 30 min, wash away excess poly-L-lysine with ultrapure water and let the slides air dry. The dry slides are ready for use.
9. Wash cells twice with 1 mL of Wash Buffer. Perform washes by centrifugation of the cells at 665 x g for 3 min. Remove the supernatant and resuspend the cells in Wash Buffer.
10. Pellet the cells by centrifugation at 665 x g for 3 min. Remove the supernatant. Resuspend the cells in 1 mL of 1.2 M sorbitol in Wash Buffer.
11. Pellet the cells by centrifugation at 665 x g for 3 min. Remove the supernatant. Resuspend the pellet in 250 µL of freshly prepared Lyticase solution to digest the cell wall. Incubate the cells in Lyticase solution for 15 min at 30 °C while shaking.
12. After digestion, wash cells 3x by centrifugation at 665 x g for 3 min and remove the supernatant. Resuspend the cells in 250 µL of 1.2 M sorbitol in Wash Buffer.
    NOTE: Because cells are fragile after cell wall digestion, resuspend them very carefully to not damage the cells.
13. Add 20 µL of resuspended cells to the poly-L-lysine coated slides. Allow them to attach to the slides for 30 min. Wash away non-adherent cells by washing the wells 3x with 50 µL of Wash Buffer.
14. Permeabilize the cell membrane by washing 3x with 50 µL of 1% Triton-X in Wash Buffer.
    NOTE: At this point the cells are ready for the proximity ligation assay protocol that will be discussed in section 4.

3. E. coli Cell Preparation

1. Prepare the following materials: PBS-T (140 mM NaCl, 2 mM KCl, 8 mM K₂HPO₄, 1.5 mM KH₂PO₄, 0.05% Tween-20), pH 7.4; lysozyme solution (2 mg/mL lysozyme, 25 mM Tris-HCl pH 8.0, 50 mM Glucose, 10 mM EDTA); 0.0001% poly-L-Lysine solution; 99% ice-cold methanol; 99% room temperature methanol; 99% acetone; 10-well diagnostic slides; a humid chamber (prepared as in step 1.1.1); tissue paper; and Coplin slide-staining jars.
2. Grow an overnight culture in Luria-Bertani (LB) medium at 30 °C while shaking.
3. Dilute the stationary culture to an OD₆₀₀ of 0.02 in fresh LB medium. Grow the cells at 30 °C while shaking until the OD₆₀₀ reaches 0.4 for log phase cells.
4. Approximately 15 min before cells reach an OD₆₀₀ of 0.4, prepare poly-L-lysine coated slides by adding 100 µL of 0.0001% poly-L-lysine to each well. Incubate the slides for 30 min at room temperature.
5. After 30 min wash away excess poly-L-lysine with ultrapure water and let slides air dry. The dry slides are ready for use.
6. When the cells reach an OD₆₀₀ of 0.4, transfer 1 mL of the culture to a sterile microcentrifuge tube and pellet cells at 2,650 x g for 2 min.
7. Resuspend cells in 50 µL of LB medium.
8. Fix cells by adding 1 mL of ice-cold 99% methanol. Mix very gently by hand. Incubate cells for 30 min at -20 °C.
9. After fixation add 20 µL of the cells to the poly-L-lysine coated slides. Let the slides air dry for 30 min.
10. Add 50 µL of freshly prepared lysozyme solution to each well to digest the cell wall. Incubate in a humid chamber for 30 min at 25 °C.
11. Remove the lysozyme solution from the wells by adding a tissue paper to the edge of the well. Wash slides 3x in 100 mL of PBS-T. Perform each wash in a Coplin slide-staining jar for 30 s, without shaking.
12. Remove wash buffer from the slides by tapping the slides on a tissue paper.
13. Permeabilize the cell membranes by adding 50 µL of 99% methanol to each well. Incubate for 1 min at room temperature.
14. Remove methanol by placing a tissue paper to the edge of the well.
15. Add 50 µL of 99% acetone to each well. Incubate for 1 min.
16. Remove excess acetone by placing a tissue paper to the edge of the well. Allow slides to air dry. At this point the cells are ready for the proximity ligation assay protocol that will be discussed in section 4.

4. Proximity Ligation Assay

1. Prepare the following materials: Blocking Buffer; Antibody Dilution Buffer; Wash Buffer ‘A’ – (10 mM Tris, 150 mM NaCl, 0.05% Tween-20) pH 7.4; Wash Buffer ‘B’ – (200 mM Tris, 100 mM NaCl) pH 7.4; Anti-Rabbit Secondary Antibody PLUS; Anti-Mouse Secondary Antibody MINUS; 5x Ligation Buffer; ligase; 5x Amplification Buffer (Orange: λ_ex 554 nm; λ_em 576 nm); polymerase; ultrapure water; and mounting medium containing DAPI.
   NOTE: The PLA detection reagents are also available in the variants Green (λ_ex 495 nm; λ_em 527 nm), Red (λ_ex 594 nm; λ_em 624 nm), FarRed (λ_ex 644 nm; λ_em 669 nm) or Brightfield (horseradish peroxidase (HRP) conjugated).
2. Block the cells by adding a drop of Blocking Buffer to each well. Incubate for 30 min at 37 °C in a humid chamber.
3. Prepare antibody solutions by diluting stock antibodies in Antibody Dilution Buffer. For each well 40 µL of antibody solution is required.
4. Remove blocking buffer by placing a tissue paper at the edge of the well. Add 40 µL of antibody diluted in Antibody Dilution Buffer to each well. Incubate for 60 min in a humid chamber at 37 °C or overnight at 4 °C.
5. Remove antibody solution from the wells by placing a tissue paper at the edge of the well. Wash slides 2x in 100 mL of Wash Buffer ‘A’ in a Coplin slide-staining jar for 5 min, without shaking.
6. During the wash steps, dilute 5x secondary antibody probes, anti-rabbit PLUS & anti-mouse MINUS (the species specificity of the probes depends on the primary antibodies used), in Antibody Dilution Buffer. Prepare 40 µL of antibody solution per well.
7. Add 40 µL of secondary antibody solution to each well. Incubate for 60 min at 37 °C in a humid chamber.
8. Remove secondary antibody solution from the wells by placing a tissue paper at the edge of the well. Wash slides 2x in 100 mL of Wash Buffer ‘A’ in a Coplin slide-staining jar for 5 min, without shaking.
9. During the washes prepare 40 µL of ligation mixture per well, by mixing 8 µL of 5x Ligation Buffer, 31 µL of ultrapure water and 1 µL of ligase.
10. Add 40 µL of ligation mixture to each well. Incubate for 30 min at 37 °C in a humid chamber.
11. Remove ligation mixture from the wells by placing a tissue paper at the edge of the well. Wash slides 2x in 100 mL of Wash Buffer ‘A’ in a Coplin slide-staining jar for 2 min, without shaking.
12. During the washes prepare 40 µL of amplification mixture per well, by mixing 8 µL of 5x amplification solution, 31.5 µL of ultrapure water, and 0.5 µL of polymerase.
    NOTE: The 5x amplification contains fluorescent probes. Protect this mixture from light. Also, protect the slides from light during each of the following steps. If using translucent Coplin slide-staining jars and humid chambers, wrap them in aluminum foil.
13. Add 40 µL of amplification mixture per well. Incubate for 100 min at 37 °C in a humid chamber.
14. Remove amplification mixture from the wells. Wash slides 2x in 100 mL of Wash Buffer ‘B’ in a Coplin slide-staining jar for 10 min without shaking.
15. Wash slides in 100 mL of Wash Buffer ‘B’ diluted 1:100 in ultrapure water in a Coplin slide-staining jar for 30 s.
16. Add 20 µL of DAPI containing mounting medium per well to the slides. Close slides with a coverslip and seal slides with nail polish.
17. If imaging, immediately incubate DAPI containing mounting medium for 10–15 min, while protected from light. If not, store the slides at -20 °C for up to 1 week, protected from light.

5. Detection

1. Use confocal microscopy to acquire images of HeLa, S. cerevisiae and E. coli cells with 20x/0.8 NA, 63x/1.4 NA and 100x/1.4 NA Plan Apochromat objectives, respectively. Excite DNA-stained DAPI with a 405 nm pulsed diode laser. For the PLA signal (for this study) excite with a 561 nm solid-state laser.

Results

Our previous in vitro studies using purified proteins revealed that a subset of human class A and class B JDPs form transient mixed class JDP complexes to efficiently target a broad range of aggregated proteins and possibly facilitate the assembly of Hsp70-based protein disaggregases⁷. We employed PLA to determine whether mixed class (A+B) JDP complexes occur in human cervical cancer cells (HeLa). Human JDPs DNAJA2 (class A) and DNAJB1 (class B) were targeted with highly specific primary antibodie...

Discussion

Co-immunoprecipitation and co-localization based approaches have been used as long-standing methods to characterize protein assembles. The detection of transiently formed specific chaperone complexes is a major challenge with such conventional methods, and as a result, previous findings are largely restricted to qualitative  interpretations. The cell lysis-based co-immunoprecipitation techniques often require cross-linking to stabilize protein-protein interactions. Cell lysis increases the risk of disrupting tr...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
37% Formaldehyde	Merck	103999
Acetone	Sigma-Aldrich	32201
anti-DNAJA2 antibody	Abcam	ab157216
anti-DNAJB1 Antibody	Enzo Life Sciences	ADI-SPA-450
anti-DnaK antibody	In house
anti-mCherry antibody	Abcam	ab125096
anti-Sis1 Antibody	Cosmo Bio Corp	COP-080051
anti-Ydj1 antibody	StressMarq Biosciences	SMC-150,
anti-YFP antibody	In house
Coplin slide-staining jar	Sigma-Aldrich	S5516
Diagnostic slides	Marienfeld	1216530
DMEM	Thermo-Fischer	31966021
DuoLink In Situ Detection Reagents Orange	Sigma-Aldrich	DUO92007
DuoLink In Situ Mounting Medium + DAPI	Sigma-Aldrich	DUO82040
DuoLink In Situ PLA Probe Anti-Mouse MINUS	Sigma-Aldrich	DUO92004
DuoLink In Situ PLA Probe Anti-Rabbit PLUS	Sigma-Aldrich	DUO92002
DuoLink In Situ Wash Buffers, Fluorescence	Sigma-Aldrich	DUO82049
Fetal Calf Serum	Thermo-Fischer	10082147
Lysozyme	Sigma-Aldrich	62971
Methanol	Sigma-Aldrich	32213
Paraformaldehyde	Sigma-Aldrich	P6148
Penicillin/Streptomycin	Thermo-Fischer	15070063
Poly-L-Lysine	Sigma-Aldrich	P47-07
Sorbitol	Sigma-Aldrich	S7547
Triton-X100	Merck	108643
Trypsin	Thermo-Fischer	25300096
Tween-20	Sigma-Aldrich	P1379
Zymolase 100T / / Lyticase	United States Biological	Z1004