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Mammalian Toll-like receptors (TLRs) 3, 7, 8 and 9 initiate immune responses to infection by recognizing microbial nucleic acids1, 2; however, these responses come at the cost of potential autoimmunity due to inappropriate recognition of self nucleic acid3. The localization of TLR9 and TLR7 to intracellular compartments appears to play a role in facilitating responses to viral nucleic acids while maintaining tolerance to self nucleic acid, yet the cell biology regulating the trafficking and localization of these receptors remains poorly understood4-6. Here, we define the route by which TLR9 and TLR7 exit the endoplasmic reticulum (ER) and traffic to endolysosomes. Surprisingly, the ectodomains of TLR9 and TLR7 are cleaved in the endolysosome, such that no full-length protein is detectable in the compartment where ligand is recognized. Remarkably, though both the full-length and cleaved forms of TLR9 are capable of binding ligand, only the processed form recruits MyD88 upon activation, arguing that this truncated receptor, rather than the full-length form, is functional. Furthermore, conditions that prevent receptor proteolysis, including forced TLR9 surface localization, render the receptor non-functional. We propose that ectodomain cleavage represents a strategy to restrict receptor activation to endolysosomal compartments and prevent TLRs from responding to self nucleic acid.
The sub-cellular localization of TLR9 and TLR7 is highly regulated. While ligand recognition occurs in endolysosomes, it has been reported that most, if not all, TLR9 resides in the ER of resting cells5, 6. Curiously, analyses of N-linked glycosylation on TLR9 indicates that the protein does not traffic through the Golgi, even in activated cells5, 6. These observations have led to a model in which TLR9 is recruited directly to endolysosomes from the ER, bypassing the classical secretory pathway5. However, general mechanistic details accounting for such unusual cell biology are lacking, and the specific details of how TLR9 transport is regulated between these compartments remain largely unknown.
In order to separate ER-resident TLR9 from receptors in the endolysosome, we purified phagosomes from cells fed latex beads. To track TLR9, we used macrophage-like RAW264 cells stably expressing TLR9 with a C-terminal HA tag (RAW-TLR9 cells). We have previously shown that this epitope tag does not affect TLR9 function4. As expected, phagosome preparations were enriched for the lysosomal protein Lamp-1 while devoid of markers of other intracellular organelles and the cytosol (Fig. 1a). Surprisingly, we did not observe any TLR9 at the expected molecular weight, 150 kilodaltons (kDa). Instead, an approximately 80 kDa protein was highly enriched in the phagosomal preparation (Fig. 1a). The presence of ligand did not alter receptor translocation, as we could not detect full-length TLR9 in phagosomes containing latex beads coated with CpG oligos (Fig. 1b), despite the fact that these beads induced TLR9 signalling (Sup. Fig. 1a). In contrast, the 80 kDa protein was evident in phagosomes at the earliest timepoint examined (10 minutes) and remained equally abundant over 4 hours (Fig. 1b).
To demonstrate directly that the 80 kDa band in our phagosome preparations represented a cleaved form of TLR9, we performed pulse-chase analysis. The 80 kDa band was first detectable after 3 hours of chase, concomitant with the onset of full length receptor degradation (Fig. 1c). The 80 kDa band continued to accumulate in parallel with the degradation of full-length TLR9, peaking at 6 hours when the full-length protein was no longer detectable. These data formally demonstrate that the 80 kDa protein is a cleavage product of full-length TLR9 consisting of approximately half of the ectodomain, the transmembrane domain, and the entire cytoplasmic domain. Based on molecular weight, we estimate that cleavage occurs within or distal to leucine rich repeat (LRR) 14. Structural modelling of TLR9 suggests that the cleaved receptor adopts an abbreviated ”horseshoe” fold encompassing a region that corresponds to residues implicated in ligand-binding by TLR37, 8 (Fig. 1d). A C-terminal cleavage product of TLR9 was also present in M-CSF derived macrophages, GM-CSF derived DCs, and Flt3L-derived plasmacytoid DCs, indicating that similar processing events occur in many immunologically relevant cell types (Fig. 1e). We observed a similar cleavage product of TLR7, but not of TLR4, suggesting that receptor processing may be a general feature shared by nucleic acid sensing TLRs (Fig. 1f).
We next sought to determine where within the cell TLR9 cleavage occurs. While N-linked sugars on full-length TLR9 were sensitive to endoglycosidaseH (EndoH), the majority of the sugars on the cleaved form of TLR9 were resistant to EndoH, indicating that the truncated form of the receptor has passed through the Golgi (Fig. 2a). A similar glycosylation pattern was observed for TLR7 (Sup. Fig. 1b). In addition, a small fraction of full-length TLR9 consistently migrated slightly slower than the majority of the full-length protein (Fig. 2b, see asterisk). Interestingly, this high molecular weight band was almost entirely EndoH-resistant, in contrast to the rest of the full-length TLR9 protein, indicating that this small pool of full-length protein has also passed through the Golgi. We also observed this high molecular weight, EndoH-resistant band in pulse/chase experiments (asterisks in Fig. 1c & Sup. Fig. 1c). The band appeared after 1½ hours of chase, immediately preceding formation of the cleavage product. Furthermore, the intensity of the high molecular weight band appeared to match the intensity of the accumulated cleavage product. Collectively, these data suggest that this high molecular weight band represents the small fraction of TLR9 that exits the ER, passes through the Golgi, and is cleaved. In support of this model, cells treated with brefeldin A (BFA), a reagent that disrupts the Golgi, contained neither the high molecular weight band (1.5h chase) nor the 80 kDa cleavage product (5h chase) (Fig. 2c). Analysis of TLR9 localization by immunofluorescence microscopy corroborated our biochemical findings (Sup. Figs. 2 & 3).
To address the mechanism responsible for TLR9 sorting from the ER, we examined Unc93b19-11. Mice with a deficiency in Unc93b1 no longer respond to TLR3, TLR7 and TLR9 ligands11, and Unc93b1 can associate with TLR3, TLR7 and TLR9 which may facilitate trafficking to endolysosomes9, 10. We generated RAW cells in which Unc93b1 mRNA was knocked down by retrovirally-encoded shRNA (Fig. 3a). As expected, these cells exhibited reduced TNF-α production in response to CpG and R848 relative to control cells (Fig. 3b). Strikingly, the TLR9 cleavage product was greatly reduced in Unc93b1 knockdown cells, though full-length TLR9 was expressed at levels comparable to control cells (Fig. 3c). The high molecular weight, full-length TLR9 band was also absent in Unc93b1 knockdown cells (Fig. 3c), and TLR9 was not present in phagosomes purified from Unc93b1 knockdown cells (Fig. 3d). These data demonstrate that Unc93b1 is required for TLR9 exit from the ER. To test whether Unc93b1 is also sufficient for this exit, we overexpressed Unc93b1 in mouse embryonic fibroblasts (MEFs), which signal poorly in response to CpG oligos. Whereas we detected very little TLR9 cleavage in control cells, simply over-expressing Unc93b in MEF-Unc93b cells resulted in a 75-fold increase in the 80 kDa band (Fig. 3e). The increase in cleaved TLR9 corresponded with a robust increase in responsiveness to CpG oligos (Fig. 3f). Thus, Unc93b1 appears to control the functional pool of TLR9 by regulating exit from the ER. Furthermore, the fraction of TLR9 that exits the ER and is cleaved appears to be responsible for TLR9 signalling.
We next attempted to block TLR9 cleavage by inhibiting various cellular proteases. BafilomycinA1, an inhibitor of the vacuolar ATPase, blocks endolysosomal acidification as well as signalling by TLR9, TLR7, and TLR312. Pulse/chase analysis of RAW-TLR9 cells treated with bafilomycinA1 revealed TLR9 cleavage was completely blocked when endolysosomal acidification was inhibited (Fig. 4a). Blocking TLR9 proteolysis with baflomycinA1 also resulted in a 20-fold accumulation of the high molecular weight TLR9 species, further supporting the idea that this band is the precursor to the cleavage product.
Two recent reports have shown that inhibitors of cathepsin K (CtsK) and cathepsin B (CtsB) block TLR9 signal transduction in DCs and macrophages, respectively13, 14. To address whether specific cathepsins may be involved in TLR9 processing, we tested whether recombinant cathepsins could cleave TLR9 in vitro. We observed that recombinant CtsK and CtsS could cleave full-length TLR9 in vitro to generate an approximately 80 kDa cleavage product (Fig. 4b). While these experiments implicate cathepsin family members in TLR9 processing, we were unable to block processing using cathepsin inhibitors. Pulse/chase analysis showed that the cleaved form of TLR9 was still present in RAW-TLR9 cells treated with the broad spectrum inhibitors E64d, pepstatinA, and leupeptin as well as with specific inhibitors of CtsK, CtsB, and CtsS (Sup. Fig. 4). With the exception of a CtsB inhibitor, these compounds did not affect TLR9 signalling (Sup. Fig 4 and data not shown). Finally, we observed no defect in TLR9 signalling in macrophages and DCs from CtsS-, CtsSxL-, CtsK-, and CtsB-deficient mice (Sup. Fig. 5). Notably, these results disagree with recent work implicating CtsK and CtsB in TLR9 function13, 14, though these works relied heavily on protease inhibitors which may have off-target effects. Instead, our data suggest that none of these proteases are solely responsible for cleaving TLR9 and are consistent with an interpretation that multiple proteases are capable of processing the receptor.
The results described above strongly implicate proteolysis as a step required for TLR9 function, but they do not directly demonstrate that processed TLR9 is a functional receptor. To address this possibility, we tested whether the cleaved form of TLR9 can bind stimulatory CpG oligos. We found that TLR9 purified from phagosomes and incubated with biotinylated-CpG oligos could be efficiently precipitated using streptavidin beads (Fig. 4c). Thus, this processed form of TLR9, which is exclusively in the phagosome, is capable of recognizing ligand. We next compared CpG-binding between the full-length and cleaved forms of TLR9. The truncated receptor was pulled down more efficiently than full-length, suggesting that it may have a higher affinity for ligand (Fig 4d). This interaction was specific, as binding was disrupted by addition of non-biotinylated CpG oligo (Fig. 4d).
Since both full-length and processed TLR9 can bind ligand, we sought to determine which form is responsible for signal transduction. The adaptor MyD88 associates with TLR9 after activation, so we examined which form of the receptor recruits MyD88 in response to CpG stimulation. Remarkably, immunoprecipitation of MyD88 in activated cells pulled down only the processed form of TLR9 (Fig. 4e). We were unable to detect any association between MyD88 and the full-length receptor, demonstrating that the processed form of TLR9 is the functional form of the receptor. We next hypothesized that requiring proteolysis may reduce the likelihood that functional receptors will leak to the cell surface and encounter self nucleic acid. To test this possibility, we used a recently reported strategy of fusing Unc93b1 to a yeast protein domain, Ist2, that directs trafficking of both Unc93b1 and TLR9 to the plasma membrane10. While Unc93b1-Ist2 localized to the plasma membrane (Sup. Fig. 6a), we did not observe significantly altered TLR9 processing or signalling in Unc93b1-Ist2 expressing cells (Fig. 4f & Sup. Fig. 6b). These results suggest that a significant portion of TLR9 may avoid relocalization in Unc93b1-Ist2 cells and signal from internal compartments. Thus, we fused TLR9 directly to the Ist2 secretion sequence and examined the signalling and localization of this fusion protein. Consistent with relocalization of the receptor to the cell surface, endoH analysis indicated that the TLR9-Ist2 fusion protein passed through the Golgi but remained unprocessed (Fig. 4g. Remarkably, TLR9-Ist2 no longer responded to CpG oligos (Fig. 4h). To ensure that this lack of signalling was not due to the Ist2 domain simply interfering with the TLR9 TIR domain, we generated a TLR9-Ist2 fusion protein in which the key amino acids necessary for plasma membrane targeting have been deleted (TLR9-Ist2δ18)15. This receptor was processed (Fig. 4g) and regained the ability to respond to CpG oligos (Fig. 4h), despite the presence of the non-functional Ist2 domain at its C-terminus.
Our results reveal that compartmentalized proteolysis of TLR9 represents a key step in nucleic acid recognition. Though both full-length and processed forms of the receptor can bind ligand, only the cleaved form of TLR9 is competent for signal transduction. It remains unclear why processing is necessary for TLR9 activation. In a previous study we showed that a surface localized chimeric receptor TLR9N4C (consisting of the TLR9 ectodomain and TLR4 TM and cytosolic domains) was hyperresponsive to self DNA4. Unlike TLR9-Ist2, this receptor signals from the cell surface even when fused to Ist2 but is not processed (Fig. 4h lower panel and Ref 4). Swapping the transmembrane (TM) and cytosolic domains of TLR9 for those of TLR4 has apparently released this receptor from the processing requirement. Recent work suggests that TLR9 undergoes a membrane-proximal conformational change upon ligand binding and activation16. One possibility is that TLR9 cleavage is a prerequisite for this conformational change. This regulatory mechanism may not be required for cell surface receptors like TLR4, explaining the ability of full-length TLR9N4C to signal. Analyses comparing the structure and conformational changes of the full-length and truncated TLR9 receptors will be necessary to resolve these possibilities.
The proteolytic regulatory step described here is consistent with a model in which TLRs involved in nucleic acid sensing are translated as ”pro-receptors” in the ER and only function after being processed in the endolysosomal compartment (Fig. 4i). This scenario is conceptually analogous to the production of proteases as pro-enzymes that must be processed before they gain enzymatic activity. In this way, compartmentalized processing of TLR9 may regulate where within the cell TLR9 activation can occur. We and others have argued that restricting activation of TLR9 and TLR7 to intracellular compartments may limit responses to self nucleic acid while preserving the ability to recognize foreign nucleic acid4, 17, 18. Thus, the requirement for processing of TLR9 and TLR7 may represent an evolutionary strategy to ensure proper self/non-self discrimination based on nucleic acid recognition.
Detailed descriptions of reagents and experiments can be found in Supplementary Methods. All stable cell lines were generated by retroviral gene transfer. For phagosome isolation, RAW cells were fed latex beads (Polysciences), the cells were disrupted by Dounce homogenization, and latex bead containing phagosomes were purified on a 62%−10% sucrose step gradient in a Beckman SW40Ti centrifuge. After purification, phagosomes were lysed by addition of TritonX-100, and proteins in phagosomes were separated by SDS-PAGE and visualized by immunoblot. Pulse/chase analyses were performed by starving cells of cysteine/methionine for 1 hour, pulsing with 35S-cysteine/methionine for 45 minutes, and chasing in molar excess of unlabeled cysteine/methionine for the indicated time periods. After lysis, radiolabeled proteins were immunoprecipated and visualized by SDS-PAGE. Deglycosylation assays were performed on immunoprecipitated proteins using endoglycosidaseH or PNGaseF (both from NEB) with supplied buffers according to manufacturer's instructions. Proteins were separated by SDS-PAGE and visualized by immunoblot. In vitro proteolysis with recombinant cathepsins (Biomol) was performed according to manufacturer guidelines. For MyD88/TLR9 coimmunoprecipitations, cells were lysed in RIPA Buffer before or after stimulation with CpG, and protein complexes were precipitated with anti-FLAG matrix. For CpG binding assays, TLR9-HA containing lysates were incubated with Biotin-CpG followed by precipitation with streptavidin matrix. In both cases, precipitated proteins were visualized by SDS-PAGE followed by immunoblot. NF-κB luciferase assays were performed by transient transfection of HEK293T cells with an NF-κB luciferase reporter plasmid and the indicated expression plasmids using LTX transfection reagent (Invitrogen) according to manufacturer's instructions. C57/Bl/6 mice were purchased from Jackson Laboratories. All knockout mice have been previously described19-22. Mice were housed within animal facilities at UC Berkeley or UCSF according to IACUC guidelines.
All chemicals and reagents, unless noted otherwise, were purchased from Fisher Scientific. Anti-HA (Clone 3F10) and anti-FLAG (M2) affinity matrices were purchased from Roche and Sigma, respectively. Latex beads were purchased from Polysciences. CpG oligonucleotides (TCCATGACGTTCCTGACGTT) with phosophorothioate linkages and 5’-biotinylated CpG oligos (of the same sequence) were purchased from Invitrogen and IDT. LPS, R848, BLP and biotinylated LPS were purchased from Invivogen. All antibodies for flow cytometry and ELISAs were purchased from eBioscience. The following antibodies were used for immunoblotting: anti-HA (Roche), anti-FLAG M2 (Sigma), anti-calnexin (Stressgen), anti-HSP90B (Thermo Scientific), anti-Lamp1 (Santa Cruz), anti-tubulin (EMD), anti-nuclear pore complex (Covance), goat anti-rat-HRP and sheep anti-mouse HRP (GE Amersham).
C57Bl/6 and 129Sv mice were purchased from Jackson Laboratories. TLR2−/−xTLR4−/−xTLR9−/− mice were generated by intercrossing individual knockout mice, kindly provided by Dr. S. Akira (Osaka University). CtsK−/−21, CtsS−/−22, and CtsSxL−/−20 mice (all backcrossed to C57Bl/6) and CtsB−/−19 mice (on the 129Sv background) have been previously described. All mice were housed within the animal facilities at the University of California at Berkeley or University of California at San Francisco according to IACUC guidelines.
RAW264 cells were purchased from ATCC and cultured in RPMI supplemented with 10% FCS, L-glutamine, penicillin/streptomycin, sodium pyruvate, and HEPES (all from Invitrogen). Unless otherwise noted, stable lines were generated by transducing cells with MSCV2.2 retroviruses encoding the target cDNA. For RAW-TLR9, RAW-TLR7 and RAWTLR4 cells, cDNA encoding the HA epitope was inserted at the 3’ end of each TLR. FLAG-TLR9 and FLAG-MyD88 have been previously described23. Unc93b-Ist2 was constructed as previously described10. TLR9-Ist2 and TLR9N4C-Ist2 were made by fusing the 69-residue Ist2 tag to the 3’ end of TLR9-HA or TLR9N4C-HA, respectively.
Bone marrow-derived conventional DCs (cDCs), macrophages, and plasmacytoid DCs (pDCs) were differentiated, as previously described4, in RPMI supplemented with GM-CSF containing supernatant, M-CSF containing supernatant, or 25ng/ml recombinant Flt3L (R&D), respectively. To generate cDCs and pDCs expressing TLR9-HA, hematopoetic stem cells (HSCs) from TLR2−/−xTLR4−/−xTLR9−/− mice were transduced with retroviruses encoding TLR9-HA as previously described4. Briefly, mice were injected with 5-flourouracil (Sigma) to enrich for HSCs. HSCs were cultured in IL-6, IL-3 and SCF (all from R&D) over 4 days and transduced with retroviruses. After 5 days, HSCs were differentiated into cDCs or pDCs as described above.
Splenic DCs were isolated from C57Bl/6 or CtsK−/− mice by magnetic cell sorting using anti-CD11c conjugated magnetic beads (Miltenyi Biotech) and an AutoMACS cell sorter (Miltenyi Biotech). Enrichment, as measured by FACS, was greater than 70%.
Cells were lysed in RIPA buffer (50mM Tris pH 8, 150mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, 0.1% SDS) supplemented with Complete protease inhibitor cocktail (Roche). After incubation on ice, lysates were cleared of insoluble material by centrifugation. For immunoprecipitations, lysates were incubated with anti-HA matrix or anti-FLAG matrix and precipitated proteins were separated by SDS-PAGE and transferred to Immobilon PVDF membrane (Millipore). Membranes were probed with the indicated antibodies and developed by ECL chemiluminescence (Pierce). Relative band intensities were quantified by counting pixels per band using ImageJ software.
Steptavidin pull-downs were performed on cells or purified phagosomes lysed in TNT buffer (20mM Tris pH 8.0, 200mM NaCl, 1% Triton X-100) and cleared of insoluble debris. Lysates were incubated for 1h with 0.2μM biotin-CpG and/or unlabeled CpG on ice, added to streptavidin-agarose (Invitrogen, pre-blocked with 1% BSA-PBS), rotated 1h at 4°C, and washed 4 times in lysis buffer. Precipitates were boiled in SDS buffer, separated by SDS-PAGE, and probed by anti-HA immunoblot.
Co-localization studies were performed on a Zeiss 510 Axioplane META microscope. Coverslips were coated with poly-D-lysine (Sigma), washed extensively with water and allowed to dry (1h). Cells were allowed to settle overnight. The next day, coverslips were washed with PBS, fixed with 4% PFA/PBS, and permeabilized with 0.5% Triton-X/PBS. After washing with 0.1% Triton-X/PBS, cells were blocked (5% goat sera, 2% BSA, 0.1% sodium azide, 0.1% Triton-X/PBS). Slides were stained in blocking buffer with anti-FLAG, anti-HA, anti-calnexin or anti-Lamp (see antibodies used for western blot). Secondary antibodies were donkey anti-rabbit Cy5, donkey anti-rabbit Cy3, goat anti-rat Cy3, goat anti-mouse Cy3 (Jackson) or donkey anti-rat Alexa680 (Invitrogen).
Visualization of Unc93b1-GFP and Unc93b1-GFP-Ist2 was performed on a Nikon E800 fluorescent microscope. Cells were plated and fixed as described above.
Transient transfections were performed in OptiMem (Invitrogen) with LTX transfection reagent (Invitrogen) according to manufacturer's guidelines. 293T cells were transiently co-transfected with the indicated expression plasmid(s) and a plasmid encoding an NF-κB luciferase reporter (with 5 tandem NF-κB binding sites, kindly provided by Russell Vance). Cells were stimulated with 3μM CpG oligo after 24 hours and lysed by passive lysis after an additional 12 hours. Luciferase activity was measured on a LMaxII-384 luminometer (Molecular Devices).
Cells were starved for 1h in cysteine/methionine-free media, then pulsed with 0.1mCi 35S-cysteine/methionine (Perkin-Elmer). After a 45 minute pulse, cells were washed and cultured in 5mL chase media with 10,000-fold molar excess L-cysteine, L-methionine or harvested as the zero timepoint. Time points were harvested as follows: cells were washed twice in 2mL PBS and lysed in 1mL RIPA plus protease inhibitor cocktail. For protease inhibitor experiments, inhibitors were added in chase media and supplemented every two hours at the following concentrations: 50μM E64d (EMD); 100μM pepstatin A (Sigma); 100μM leupeptin (Sigma); 10nM cathepsin K inhibitor III (Cbz-Leu-NH-CH2-CO-CH2-NH-Leu-Cbz, Sigma); 30μM CtsB inhibitor (Me047, EMD); 2μM CtsS inhibitor (-Phe-Leu-COCHO • H2O, EMD). BaflomycinA1 (Sigma) was used at 50nM and BrefeldinA (Sigma) was used at 10μg/mL.
4x107 RAW cells were incubated with ~108 2μM latex beads (Polysciences) for various time points. After rigorous washing in PBS, RAW cells were scraped into 3ml sucrose homogenization buffer (SHB: 250μM sucrose, 3mM imidazole pH7.4) and pelleted by centrifugation. Cells were resuspended in 1mL SHB plus protease inhibitor cocktail (Roche) and EDTA and disrupted by 25 strokes in a steel dounce homogenizer. The disrupted cells were gently rocked for 10 minutes on ice and centrifuged at 8,000xg to remove intact cells, nuclei and gross debris. The remaining supernatant was further processed to separate intact phagosomes. 40μL was set aside as the ”lysate” sample and lysed by addition of 1% TritonX-100. The remaining supernatant was mixed with an equal volume of 60% sucrose, and applied to a sucrose step gradient as follows: 1mL 60% sucrose, 2mL homogenate, 2mL 32% sucrose, 2mL 20% sucrose, 2mL 10% sucrose. The gradient was spun at 100,000xg for 1h in a SW40 rotor. Following centrifugation, phagosomes were harvested from the 20%-10% sucrose interface. Phagosomes were diluted in 10mL PBS and spun at 40,000xg for 15 minutes in an SW40 rotor. The phagosome pellet was resuspended in 40μL SHB, protease inhibitor cocktail, EDTA and 1% TritonX-100. Protein concentrations were normalized by BCA assay, and lysates were analysed by western blot.
Recombinant cathepsin S and recombinant pro-cathepsin K were purchased from BioMol. 293T cells stably expressing TLR9-HA were lysed in RIPA buffer and TLR9 was immunoprecipitated with anti-HA agarose. Immunoprecipitates were washed 4 times in cathepsin reaction buffer (50mM potassium phosphate pH 6.5, 50mM NaCl, 2mM EDTA, 0.01% TritonX-100, 0.5mM DTT) followed by incubation with or without cathepsins. Pro-cathepsin K was activated according to manufacturer's instructions (i.e., incubation in 32.5mM NaOAc pH3.5 for 25 minutes at 24 degrees). Activated cathepsin K was immediately incubated with immunoprecipitated TLR9-HA in cathepsin reaction buffer for 45 minutes at 24°C. Cathepsin S (0.0024 units) was added directly to immunoprecipitated TLR9-HA in cathepsin reaction buffer and incubated for 45 minutes at 40°C. Enzymes were inactivated by the addition of SDS loading buffer and boiling. Reactions were resolved by SDS-PAGE and anti-HA immunoblot (as described above).
We thank members of the Barton and Vance Labs for discussions, S. Akira for providing TLR knockout mice, and R. Vance and R. Medzhitov for advice. We acknowledge the CHPS Imaging Core and Paul Herzmark for assistance with microscopy. This work was supported by a Novel Research Grant from The Lupus Research Institute (G.M.B.), the Hellman Faculty Fund (G.M.B), and NIH grants HL67204 (H.A.L), CA009179 (S.E.E.), and AI072429 (G.M.B.).
S.E.E and G.M.B. planned experiments and wrote the manuscript. S.E.E., B.L.L., L.L, and K.E.W. performed the experiments. G-P.S. and H.A.C. contributed reagents. All authors read and commented on the manuscript.