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Original Article |
Address correspondence to Joseph Sodroski, Dana-Farber Cancer Institute, 44 Binney St., JFB 824, Boston, MA 02115. Phone: 617-632-3371; Fax: 617-632-4338; E-mail: Joseph_Sodroski{at}dfci.harvard.edu
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Abstract |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
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Key Words: CCR5 • O-Glycosylation • sialic acid • tyrosine sulfation • HIV
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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, MIP-1ß, regulated on activation normal T cell expressed (RANTES), and some other ß-chemokines has been found on several cell types including memory T cells, B cells, macrophages, microglia, mast cell precursors, and dendritic cells (1–4). Together with CD4, CCR5 serves as a coreceptor facilitating the entry of HIV-1, HIV-2, and simian immunodeficiency virus (SIV) into target cells (5, 6). Primary infection with these viruses is predominantly mediated by so-called R5 viral strains that utilize CCR5. Later in the course of HIV-1 infection, X4 viral strains often emerge that utilize another chemokine receptor, CXC chemokine receptor (CXCR)4. The emergence of X4 or dual tropic R5X4 viral subtypes is typically associated with rapid deterioration of the immune system and development of AIDS (7). Approximately 1% of Caucasians are homozygous for a 32-base pair deletion in the CCR5 gene. These individuals produce a nonfunctional protein and thus are highly resistant to HIV-1 infection, demonstrating the pivotal role of CCR5 for viral transmission (8). Individuals lacking CCR5 are immunologically competent, a phenotype that may reflect the high degree of redundancy in the chemokine system. The ability of healthy individuals to withstand the absence of CCR5 has stimulated efforts to develop specific CCR5 inhibitors for antiretroviral therapy (9). Natural chemokine ligands, monoclonal antibodies, and small nonpeptide compounds like TAK-779 can inhibit HIV-1 entry in vitro (10, 11) and are being considered for in vivo applications.
Precise knowledge of the structural basis for chemokine and HIV-1 envelope glycoprotein binding to CCR5 would advance our understanding of the role of CCR5 in physiology and disease, and inform efforts to develop potent drugs for therapeutic intervention. Like other GPCRs, CCR5 has an amino terminus and three extracellular loops. The NH2 terminus and the second extracellular loop of CCR5 contribute to high affinity binding of chemokines and the HIV-1 gp120 exterior envelope glycoprotein, but other CCR5 domains can also influence these associations (12–14). A current model for chemokine binding suggests a two-step mechanism involving an initial association with the probably more exposed CCR5 NH2 terminus and a subsequent, more specific, interaction with the CCR5 extracellular loops leading to receptor activation (12, 15, 16). Deletion of the NH2-terminal sequences of CCR5 strongly impairs chemokine binding, but substitution of this domain with corresponding regions from related receptors, including CCR1, CCR2b, CXCR2, and CXCR4, can restore chemokine binding and receptor activation (12, 13, 17). Therefore, similar determinants in the NH2 terminus shared among related receptors likely contribute to high affinity binding of chemokines (13). Negatively charged and aromatic residues in the NH2-terminal region of CCR5 are crucial for the association with chemokines and the HIV-1 gp120 envelope glycoprotein (13, 14, 17–20). Sulfate moieties on tyrosines contribute extra negative charges to this region and facilitate HIV-1 entry (21). Inhibition of tyrosine sulfation substantially decreases the affinity of MIP-1, MIP-1ß, and HIV-1 gp120/CD4 complexes for CCR5 (21).
In addition to tyrosine sulfation, CCR5 is also modified by O-linked oligosaccharides (O-glycans), which are typically added to serine or threonine residues in the Golgi compartment of the cell (21). In the cell types examined to date, the O-glycans on CCR5 are not sulfated themselves but contain negatively charged terminal sialic acid residues (21). The functions of O-glycans are as diverse as their structure. These include the maintenance of protein conformation, protection of proteins from proteases, control of active epitopes and antigenicity, blood clotting, embryogenesis, development, participation in cell-egg binding, and microbe attachment to cells (22, 23). Of special interest is the contribution of sialylated O-glycans to the adhesion of activated immune cells and to the metastatic potential of cancer cells (24).
In this paper, we report the location of the major O-glycosylation site of CCR5 expressed in several cell lines as well as in primary macrophages. We analyze the contribution of CCR5 O-glycosylation to chemokine binding and HIV-1 entry. Finally, we extend our studies on tyrosine sulfation in the CCR5 NH2 terminus and investigate its role in chemokine binding.
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Materials and Methods |
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Monocyte-derived rhesus macrophages were obtained and cultured as described previously (25). Approximately 5 x 106 mononuclear cells, isolated on a Ficoll-Paque gradient, were seeded in each well of a 6-well plate and cultured in macrophage-driving medium (25) containing 50 U GM-CSF and 5 U M-CSF. Nonadherent cells were removed every second day by extensive washes with PBS.
Plasmids.
A previously described pcDNA3.1-based expression plasmid (26) for human codon-optimized CCR5 with a COOH-terminal C9 tag (TETSQVAPA) was used as a template to generate CCR5 mutants. The mutations specifying changes in the CCR5 NH2 terminus were introduced by PCR amplification using Pfu-polymerase and 5'-primers with changes of serine/threonine codons into alanine codons, along with appropriate restriction sites for cloning. The 5' primers were as follows, with the mutated nucleotides underlined: AATS mutant: GAATTCAAGCTTGCCGCCGCCATGGACTACCAGGTGGCGGCGCCCATCTACGACATCAACTACTAC; SSAA mutant: GAATTCAAGCTTGCCGCCGCCATGGACTACCAGGT-GTCCTCCCCATCTACGACATCAACTACTACGCGGCG- GAGCCCTGCCAGAAGATC; AAAA mutant: GAATTCAAGCTTGCCGCCGCCATGGACTACCAGGTGGCGGCG-CCCATCTACGACATCAACTACTACGCGGCGGAGCCCTGCCAGAAGATC; ASTS mutant: GAATTCAAGCTTGCCGCCGCCATGGACTACCAGGTGGCGTCCCCCATCTACGACATCAACTACTAC; SATS mutant: GAATTC-AAGCTTGCCGCCGCCATGGACTACCAGGTGTCCGCGCCCATCTACGACATCAACTACTAC.
The 3' primer for all of the above mutants anneals to the region encoding the C9 tag of the CCR5 gene and has the following sequence: CCTCTAGACTCGAGCGGCCGCTTAGGCGGGGGC. The mutated CCR5 genes were amplified by PCR and ligated into the pcDNA 3.1 vector using the HindIII and NotI restriction sites. Analogous amplified fragments were also cloned into the pSIvec1
env plasmid (25) using AgeI and NotI restriction sites and sequenced to confirm the alterations. The plasmids pSIvec1envhuCCR5, pHCM-vesicular stomatitis virus G protein (VSV-G), and psrev used to generate VSV G-pseudotyped viruses encoding huCCR5 are described in (25) and references therein.
The QuikChange Mutagenesis kit (Stratagene) was used to generate the CCR5 mutants with serine/threonine residues in the second and third extracellular loops changed to alanine. The primers were as follows (only one primer for each mutant is shown, as the second primer was simply the reverse complement): second extracellular loop mutant: CAGAAGGAGGGCCTGCACTACGCGTGCGCCGCCCACTTCCCCTACTC-CCAG; third extracellular loop mutant: CAGGAGTTCTTCGGCCTGAACAATTGCGCCGCCGCCACCGCCTGG-ACCAGGC. MluI and MfeI restriction sites were engineered into the respective primers to allow for identification of positive clones, which were subsequently sequenced. The mutant CCR52–17 was generated in a similar way, using a 5'-primer encoding a deletion of the sequence coding for amino acids 2–17.
Cf2Th cells stably expressing human CCR5 variants were established by transfection using the calcium phosphate method and G418 selection. Cells expressing high and comparable surface levels of wild-type and CCR5 mutants, based on staining with dialyzed phycoerythrin-conjugated 2D7 antibody (BD PharMingen), were selected by sorting on a MoFlo FACS® (Cytomatics) machine and cultured in the presence of G418. To maintain consistent expression levels, it was necessary to resort the stable cell lines intermittently. LdlD cells stably expressing human CCR5 were established using the same approach.
Transient expression of CCR5 variants was achieved by transfecting Cf2Th, Cf2Th-CD4, HEK 293T, HeLa, and CHO cells with 25 µg of each expression vector using the calcium phosphate method. Two days after transfection, the surface expression level of CCR5 was determined using phycoerythrin-conjugated 2D7 or 3A9 antibodies (BD PharMingen). Transfectants showing less than 25% variation in expression of the different CCR5 variants were used for immunoprecipitation, chemokine binding, or virus entry experiments.
To express human CCR5 and glycosylation mutants in primary rhesus macrophages, recombinant VSV G-pseudotyped viruses were produced in HEK 293T cells. Recombinant viruses were generated using the SHIV-derived vector pSIvec1envhuCCR5 or analogous vectors (25) with changes of serines/threonines in the CCR5 sequence, as described above. Macrophages were transduced overnight with 30,000 reverse transcriptase (RT) units of virus. 48 h later, the macrophages were lysed and the CCR5 protein was immunoprecipitated.
Labeling, Immunoprecipitation, and Glycosidase Treatment of CCR5 Variants.
To label and immunoprecipitate the CCR5 proteins, all cells but macrophages were grown to confluency in 10-cm dishes. Primary macrophages were cultured in 6-well plates and 2–3 wells were used for each CCR5 variant. Cells were washed with PBS and labeled overnight with [35S]cysteine/methionine in cysteine- and methionine-free medium or with [3H]galactose in glucose-free medium. Cells were then washed with PBS and lysed using 1 ml lysis buffer consisting of 100 mM (NH4)2SO4, 20 mM Tris-HCl (pH 7.5), 10% glycerol, 1% Cymal-5 (Anatrace), 0.1% SDS, and one tablet of CompleteTM Protease Inhibitor Mixture (Roche) per 50 ml. Labeled receptor was immunoprecipitated using the C9 tag-specific 1D4 antibody (National Cell Culture Center) covalently linked to Sepharose beads (Amersham Pharmacia Biotech). Precipitates were washed five times in lysis buffer, incubated at 56°C for 20 min in reducing sample buffer, analyzed by 10% SDS-PAGE, and visualized by autoradiography.
For removal of O-glycan chains, Sepharose beads containing the immunoprecipitated CCR5 proteins were washed twice with PBS to remove detergent, divided, and one half was treated overnight at 37°C with an O-glycosidase mix (2–3,6,8,9-neuraminidase, ß1,4-galactosidase, endo--N-acetylgalactosaminidase, and ß-N-acetylglucosaminidase present in the Glycoprotein Deglycosylation Kit from Calbiochem.
To remove sialidase moieties from CCR5 present on the cell surface, 2 x 107 cells were detached with 5 mM EDTA in PBS, washed once with medium, and 50% of the cells were treated for 1.5 h at 37°C with 0.3 U of sialidase from Arthrobacter ureafaciens (Roche) in 200 µl medium without FCS and 0.1% sodium azide. The other 50% were incubated in the same medium under the same conditions, but without enzyme. Cells were then used for immunoprecipitation or for chemokine binding assays.
Chemokine Binding Assay.
Cells were detached from the flasks with 5 mM EDTA in PBS, washed with medium without FCS, counted, and resuspended in binding buffer (50 mM HEPES, pH 7.5, 150 mM NaCl, 1 mM CaCl2, 5 mM MgCl2, and 5% dialyzed FCS). Competition binding assays were performed for 1 h at 37°C with 5 x 105 cells, 0.1 nM 125I-labeled chemokine (Dupont NEN) and varying concentrations of cold chemokine (100 pM-1 µM) in 100 µl volumes. Cells with bound chemokines were washed twice with binding buffer and counted in a gamma counter. In parallel with the binding experiment, the expression level of each CCR5 variant was analyzed with phycoerythrin-conjugated 2D7 and/or 3A9 antibody on a FACScanTM cytometer (Becton Dickinson) with CELLQuestTM software. Binding data were analyzed using GraphPad Prism software running an algorithm for nonlinear regression of homologous one-site competition binding with ligand depletion (27) to obtain relative Kd values.
Calcium Mobilization by CCR5 Variants.
Chemokine-induced Ca2+ influx in Cf2Th cells stably expressing different CCR5 variants was measured after transfecting these cells with a plasmid encoding the G protein component G16. Preliminary experiments showed that G16 expression strongly enhanced ligand-triggered Ca2+ influx into CCR5-expressing Cf2Th cells. Cells were loaded with the indicator dye Fura 2/AM (Molecular Probes) for 1 h at 37°C in 20 mM Hepes, pH 7.4, 125 mM NaCl, 1 mM CaCl2, 1 mM MgCl2, 5 mM KCl, 0.5 mM glucose, and 0.2% BSA. Cells were then washed twice in the same buffer without dye and resuspended in new buffer at a density of 2 x 106/ml. Changes in intracellular Ca2+ concentration in response to chemokine binding were measured by monitoring the emission at 510 nm of the excitations at 340 and 380 nm as a function of time.
Virus Entry Assay.
The efficiency of HIV-1 entry into cells was determined using pseudotyped single-round viruses encoding a chloramphenicol acetyltransferase (CAT) reporter gene in a previously published env complementation assay (6). The recombinant HIV-1 were generated in HeLa cells by using the pHXBH10envCAT vector and plasmids encoding HIV-1 or SIVmac envelope glycoproteins as previously described (6, 25). Cf2Th cells stably expressing human CD4 were transiently transfected with plasmids encoding the CCR5 variants to be tested. Cells expressing similar CCR5 levels, as determined by staining a cell sample with the 2D7 antibody at 48 h after transfection, were seeded in 6-well plates and infected with 5,000 RT units of a single-round virus for 1 h. 3 d after infection, CAT activity was measured to assess the efficiency of virus entry.
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Results |
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2–17) that was efficiently expressed on the cell surface, as documented by staining with the 2D7 anti-CCR5 antibody (data not shown). The CCR52–17 protein migrated with an apparent molecular mass that is 4–5 kD less than the 43 kD mass of the wild-type CCR5 (Fig. 1 B). The CCR52–17 mutant did not incorporate galactose, a sugar found in most O-glycosylated mammalian membrane proteins. This implies that in Cf2Th cells the extracellular loops of CCR5 are not modified by galactose-containing carbohydrate chains. This interpretation was supported by our analysis of CCR5 mutants with alterations of clusters of serines/threonines in the second and third extracellular loops (residues 177/179/180 and 270–272, respectively; Fig. 1 A). When these residues were altered to alanines, no change in the migration of the CCR5 protein on SDS-polyacrylamide gels was observed (data not shown). We conclude that efficient O-linked glycosylation of CCR5 is dependent upon NH2-terminal sequences.
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2-kD decrease in molecular mass. The identical result was observed for the SSAA mutant, indicating that threonine 16 and serine 17 are not required for O-glycosylation of CCR5 in Cf2Th cells. The AATS and AAAA mutants migrated with an apparent molecular mass that was 2 kD less than that of wild-type CCR5. Compared with the wild-type protein, an increase in the amount of the CCR5 precursor was observed for these mutants. The migration of the AATS and AAAA mutants was not affected by glycosidase treatment. Similar results were obtained by labeling the cells with [35S]sulfate (data not shown), indicating that the introduced amino acid changes and consequent effects on O-glycosylation do not prevent tyrosine sulfation of CCR5. The results suggest that a major O-glycosylation site on human CCR5 expressed in Cf2Th cells involves serines 6 and 7. To characterize the site of CCR5 O-glycosylation further, we created the ASTS and SATS mutants, which have single serine residues at positions 6 and 7, respectively, converted to alanines. Cf2Th cells expressing comparable surface levels of CCR5 variants were labeled either with [35S]cysteine/methionine or [3H]galactose, lysed and used for precipitation by the 1D4 antibody directed against the C9 peptide tag. Comparison of Figs. 1 D ([35S]cysteine/methionine labeling) and 1 E ([3H]galactose labeling) indicates that the ASTS and SATS mutants resembled the wild-type CCR5 both in mobility characteristics and in the intensity of labeling with [3H]galactose. These results suggest that either serine 6 or 7 can be modified by O-linked glycans, and that only one of these two potential sites is extensively modified on the wild-type CCR5 protein.
As expected, the AAAA mutant did not incorporate [3H]galactose (Fig. 1 E), consistent with the results obtained with the CCR52–17 mutant suggesting that all of the galactose-containing glycans on CCR5 are located in the NH2 terminus of the protein. Of interest, the AATS mutant did incorporate [3H]galactose, but much less efficiently than wild-type CCR5. The lack of [3H]galactose labeling of the AAAA mutant indicates that galactose addition to the AATS mutant is dependent upon threonine 16 and/or serine 17. The lower level of galactose incorporation and the absence of detectable migration differences after glycosidase treatment of the AATS mutant suggest that glycosylation at threonine 16 and/or serine 17 is much less efficient or involves a smaller O-glycan with fewer galactose moieties, compared with O-glycosylation of serines 6 and 7.
O-glycosylation of CCR5 in Different Cells.
The O-glycosylation pattern of a protein may vary, depending on the expressing cell type (24). To examine the O-glycosylation pattern in other cell types and compare it with the results obtained in Cf2Th cells, we transiently expressed wild-type CCR5 as well as the AATS and SSAA mutants in the human embryonic kidney line 293T (HEK 293T), in HeLa cells (a human cervical carcinoma line), and in primary rhesus monkey macrophages. The expressed proteins were precipitated from lysates of [35S]cysteine/methionine-labeled cells and analyzed by SDS-PAGE. Similar to the results seen in Cf2Th cells, the AATS variant migrated, in all cells tested, with an apparent molecular mass 2 kD less than that of the wild-type protein (Fig. 2). We conclude that in all the cell types examined, the CCR5 serines at positions 6 and 7 are major sites of O-glycosylation.
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15–25% reduced compared with that of wild-type CCR5. Because virus entry associated with even the glycosylated SSAA mutant was affected, this marginal reduction is not necessarily caused by a lack of O-glycosylation and might represent a result of the amino acid alterations per se.
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and MIP-1ß. Cf2Th cells stably expressing comparable levels of wild-type, AATS, SSAA, and AAAA variants of CCR5 were selected by fluorescence-activated cell sorting, using a phycoerythrin-conjugated 2D7 antibody that recognizes a conformation-dependent epitope in the second extracellular loop of CCR5. The expression level of CCR5 on these cells was tested in parallel with each binding experiment, using the 2D7 antibody and the 3A9 antibody, which recognizes a linear epitope in the CCR5 NH2 terminus (data not shown). As shown in Fig. 4 A, [125I]MIP-1 bound to cells expressing the SSAA mutant with a slightly higher affinity than to cells expressing wild-type CCR5 (measured dissociation constants of 0.91 ± 0.8 nM and 1.6 ± 0.9 nM for SSAA and wild-type CCR5, respectively). More interestingly, MIP-1 exhibited dramatically impaired binding to cells expressing the AATS and AAAA mutants, which are not efficiently O-glycosylated (Fig. 4 A). Almost identical binding results were obtained using MIP-1ß (Fig. 4 B). MIP-1ß also bound slightly more efficiently to the SSAA mutant (Kd value of 2.06 ± 0.5 nM) than to the wild-type receptor (Kd of 7.2 ± 0.6 nM). Binding of MIP-1ß to the AATS and AAAA mutants was significantly impaired but was higher than the negligible binding of MIP-1 to these variants.
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and MIP-1ß with the glycosylation-deficient AATS mutant resulted in reduced efficiency of Ca2+ mobilization. As shown in Fig. 4, C and D, the peak Ca2+ influx after a stimulation of Cf2Th cells expressing the AATS variant with 10 nM chemokine is 3–5 times lower than that seen in cells expressing similar levels of wild-type receptor or the SSAA mutant. We also examined the binding affinities of MIP-1ß to the SATS and ASTS mutants, which can be O-glycosylated at serine 6 and 7, respectively. Cf2Th transfectants transiently expressing similar surface levels of the CCR5 variants were used for binding assays. The SATS variant bound MIP-1ß with an affinity comparable to that of wild-type CCR5, but MIP-1ß association with the ASTS mutant was significantly less efficient (relative Kd value of 19.9 ± 1.3 nM) (Fig. 4 E). Thus, O-glycosylation of serine 6 on CCR5 is optimal for MIP-1ß binding.
Chemokine Binding to O-glycosylation–defective CHO Cells Expressing Human CCR5.
The CHO-derived ldlD cells lack the epimerase needed to synthesize UDP-galactose and UDP-N-acetylgalactosamine from UDP-glucose or UDP-N-acetylglucosamine, respectively (29). This defect completely prevents O-glycosylation of proteins and impairs maturation of N-linked carbohydrate chains (29). This phenotype can be reversed by addition of Gal and GalNAc to the cell culture media. To confirm that O-glycosylation of CCR5 is necessary for high affinity binding of chemokines, we generated ldlD cells stably expressing human CCR5 with a C9 tag to perform binding experiments. The 1D4 antibody directed against the C9 peptide tag was used to precipitate CCR5 from the lysates of labeled ldlD-CCR5 cells cultured in Gal/GalNAc-deficient medium. CCR5 in these cells migrated with an apparent molecular mass 2–3 kD smaller than that of CCR5 from cells grown in the same medium supplemented with 50 µM Gal/500 µM GalNAc (Fig. 5 A). The CCR5 from the ldlD-CCR5 cells cultured in Gal/GalNAc-supplemented medium migrated comparably to CCR5 expressed in the parental CHO cells. These results are consistent with the expected O-glycosylation of CCR5 in the ldlD-CCR5 cells that is conditionally dependent upon the availability of Gal/GalNAc.
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and MIP-1ß were performed with the ldlD-CCR5 cells. Addition of Gal/GalNAc to the medium did not significantly change the staining of the cells with phycoerythrin-conjugated 2D7 antibody (Fig. 5 legend), suggesting that the glycosylation state of CCR5 does not greatly affect surface expression of the protein in ldlD cells. Binding of both MIP-1 and MIP-1ß was significantly lower to ldlD-CCR5 cells grown in Gal/GalNAc-deficient medium than to these cells cultured in Gal/GalNAc-containing medium (Fig. 5, B and C). No specific binding of either chemokine was detected to ldlD cells lacking CCR5. These results confirm the importance of O-glycosylation for the ability of wild-type CCR5 to bind its chemokine ligands.
Contribution of Sialic Acid Moieties on the CCR5 O-glycan to Chemokine Binding.
A common modification of O-linked carbohydrate chains is the addition of sialic acid residues by sialyltransferases. The important role that negative charges in the NH2 terminus of CCR5 play with respect to ligand binding prompted us to examine the effect on chemokine binding of removing only sialic acids from the CCR5 O-glycan. A 1.5-h treatment of 35S-labeled Cf2Th cells expressing wild-type CCR5 with 0.3 units of sialidase from Arthrobacter ureafaciens, which hydrolyzes terminal 2–3, 2–6, and 2–8-linked acylneuraminic acids, led to a visible shift in migration of the immunoprecipitated CCR5 band on SDS-PAGE (Fig. 6 A). In the presence of 0.1% sodium azide to prevent receptor internalization, sialidase treatment had no effect on the expression level of CCR5, as determined by staining cells with phycoerythrin-conjugated 2D7 antibody (data not shown). Binding of MIP-1 and MIP-1ß to sialidase-treated Cf2Th cells expressing wild-type CCR5 was almost completely abolished (Fig. 6, B and C). As expected, no specific binding of chemokines to the CCR5 NH2-terminal deletion mutant, CCR52–17, could be detected (Fig. 6 B, and data not shown).
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and MIP-1ß (21). To examine the contribution of specific CCR5 NH2-terminal tyrosine sulfates to chemokine binding, CCR5 mutants with alterations in one or more of the tyrosines at positions 3, 10, 14, and 15 were used. Cf2Th cell lines expressing comparable levels of the mutants were established, and equivalent surface expression of the CCR5 variants was verified by 2D7 antibody staining in parallel with the binding assays. The CCR5 mutants are named according to the amino acid residues located at positions 3, 10, 14, and 15. Previous studies (21) demonstrated that alteration of all four NH2-terminal CCR5 tyrosines to phenylalanine (FFFF) or to aspartic acid (DDDD) resulted in a loss of sulfate incorporation. Restoration of individual tyrosines in the context of the DDDD mutant resulted in mutant proteins (YDDD, DYDD, DDYD, and DDDY) that incorporated sulfate (21). Thus, all of the CCR5 NH2-terminal tyrosines can potentially be sulfated, and the study of mutants (FDDD, DFDD, DDFD, and DDDF) in which the restored tyrosines are converted to phenylalanine allows an assessment of the contribution of sulfation of a specific tyrosine to a phenotype. Changes in all four NH2-terminal CCR5 tyrosines resulted in 70–200-fold decreases in the affinity of MIP-1 and RANTES (Table I). Restoration of tyrosine 3 in the YDDD mutant did not restore the efficient binding of MIP-1. Restoration of tyrosines 10, 14, and 15 all resulted in improved chemokine binding in the context of the DDDD mutant. In the case of tyrosine 14, this improvement was significantly better for the restoration of tyrosine than for a phenylalanine substitution. This suggests that, for both MIP-1 and RANTES, the presence of sulfation on tyrosine 14 contributes to the interaction with CCR5. By similar reasoning, the data in Table I suggest that the sulfation of tyrosine 15 contributes to the binding of RANTES but not that of MIP-1. Thus, chemokine binding is facilitated by sulfation of NH2-terminal CCR5 tyrosines, particularly tyrosine 14 and, for RANTES, tyrosine 15.
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Discussion |
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As an initial step in evaluating the functional significance of CCR5 glycosylation, we characterized the location and extent of this modification. Glycan chains are commonly added to chemokine receptors, either by N-linkage to an asparagine residue in the sequon asparagine-X-serine/threonine or by O-linkage to a serine or threonine. CCR5 contains one potential N-linked glycosylation site (asparagine 268 - cysteine 269 - serine 270) in the third extracellular loop, but this site is not used (21, 31). Cysteine 269 in the consensus sequence is thought to be involved in the formation of a disulfide bond with cysteine 20 in the NH2 terminus, perhaps limiting the accessibility of this region to glycosyltransferases. CCR5 has been shown to be O-glycosylated (21) and has four serine/threonine-rich regions in its extracellular domains. Our mutagenic analysis of these regions indicates that the major CCR5 O-glycosylation site in all cells tested, including primary macrophages, involves a pair of serines at positions 6 and 7. A mutant CCR5 protein with serine to alanine changes at these positions demonstrated an 2-kD shift on SDS-PAGE and migrated with the same mobility as enzymatically deglycosylated wild-type protein. The ASTS and SATS mutants, in which serine 6 and 7, respectively, are individually converted to alanine, migrated similarly to the wild-type CCR5 protein. This result indicates that either serine 6 or serine 7 can be glycosylated but only one of them is modified in wild-type CCR5.
Our studies suggest that a second potential O-glycosylation site in the CCR5 NH2 terminus, at threonine 16/serine 17, can be modified by galactose-containing glycans under some circumstances. The AATS mutant, in which serines 6 and 7 are converted to alanines, incorporated galactose at a reduced level compared with the wild-type CCR5. This galactose incorporation was abolished by the additional conversion of threonine 16 and serine 17 to alanines in the AAAA mutant, indicating the dependence of this modification on the second potential O-glycosylation site in the CCR5 NH2 terminus. The AATS and AAAA mutants labeled with [35S]cysteine/methionine migrated indistinguishably on SDS-polyacrylamide gels. Furthermore, enzymatic deglycosylation of the AATS mutant does not result in a detectable shift in its migration. These observations suggest that the sugar moiety added to either threonine 16 or serine 17 in the AATS mutant is relatively small and likely consists of a T antigen structure (Gal ß1–3 GalNAc - Ser/Thr).
It is unclear whether O-glycosylation of either threonine 16 or serine 17 occurs in wild-type CCR5. The comparable migration and efficiency of galactose incorporation observed for wild-type CCR5 and the SSAA mutant in which threonine 16 or serine 17 are both converted to alanines, indicate that any O-glycosylation at this site involves short glycan chains. It is also quite possible that preventing glycosylation at the preferred site, serines 6 and 7, in the AATS mutant promotes aberrant glycosylation at threonine 16/serine 17. A similar effect has been reported for vasopressin receptor 2, where the removal of one glycosylation site resulted in other sites becoming available to glycosyltransferases (32). Our most extensive studies were performed in Cf2Th cells and it should be kept in mind that utilization of the potential O-glycosylation site at threonine 16 and serine 17 could vary with cell type or the differentiation or activation state of the cell (24).
Efficient O-glycosylation of CCR5 appears to be limited to the NH2 terminus, based on the phenotypes of the CCR52–17 and AAAA mutants. The serine/threonine-rich regions in the CCR5 second and third extracellular loops occur adjacent to cysteine residues involved in disulfide bonds. Like the potential N-glycosylation site, these potential sites of O-glycosylation may not be accessible due to close interactions of these regions with other elements of the CCR5 ectodomain.
To date, only a few instances of O-glycosylation of GPCRs have been documented (32) and little is known about the presence of this modification on chemokine receptors and its potential contribution to the physiologic function of these proteins. The results of our homologous competition binding experiments and Ca2+ mobilization assays performed with MIP-1 and MIP-1ß demonstrate that O-glycosylation of CCR5 at serine 6 or 7 is necessary for high affinity binding of both chemokines. Results analogous to those obtained with CCR5 mutants were observed for the wild-type CCR5 expressed in ldlD cells, which are conditionally defective for O-linked sugar addition. Most of the contribution of the O-linked glycans on CCR5 to chemokine binding appears to depend upon the negatively charged sialic acids. The sialic acids likely make specific contacts with basic residues on the chemokine surface thought to interact with CCR5 (33, 34). The binding of MIP-1 was disrupted more than that of MIP-1ß by removal of the CCR5 O-glycans or sialic acid, suggesting different degrees of contact between the negatively charged glycans and the binding surfaces of different chemokine ligands.
The chemokine binding studies provide clues that serine 6 is the preferred site of O-glycosylation on wild-type CCR5. The SATS mutant, in which serine 7 is changed to alanine, bound chemokine with an affinity comparable to that of wild-type CCR5. This is consistent with other mutagenic studies of CCR5 in which serine 7 was altered (13). By contrast, replacement of serine 6 with alanine (ASTS mutant) resulted in a decreased chemokine binding affinity of 3–4-fold, despite the O-glycosylation of this mutant at serine 7. A similar decrease in chemokine binding has been observed for a CCR5 mutant in which serine 6 is converted to proline (33). Thus, although O-glycosylation at serine 7 contributes somewhat to chemokine binding, the presence of O-linked glycans on serine 6 is optimal for the interaction of CCR5 with chemokine ligands. Because MIP-1ß binds comparably to wild-type CCR5 and the SATS mutant, but binds less well to the ASTS mutant, the wild-type CCR5 probably is O-glycosylated predominantly on serine 6.
Further studies will be required to define the structure of the O-glycans added to CCR5. CHO cells do not express core 2 ß1,6-N-acetylglucosaminyltransferase and 1,3-fucosyltransferase (35) and, as a result, O-linked carbohydrates added to proteins produced in CHO cells are typically relatively short, core-1 O-glycans (36–43). Our data demonstrating MIP-1 and MIP-1ß binding to CCR5 expressed in CHO or IdID cells indicate that the addition of such core-1 structures is sufficient to allow the interaction with chemokines.
It has been shown previously that glycosylation is required to maintain high-affinity SDF-1 binding (44) and influences the ability of CXCR4 to serve as a coreceptor for T-tropic (X4) and dual-tropic (R5X4) HIV-1 strains (45). Removal of a site of N-linked glycosylation allows CXCR4 to serve as a more universal coreceptor, allowing efficient entry of several HIV-1 isolates that normally use only CCR5 (45). We tested the impact of O-glycosylation on the ability of CCR5 to serve as a coreceptor for HIV-1 and SIV. The absence of O-glycans on CCR5 did not significantly influence HIV-1 and SIV entry efficiency. It is possible that such an influence might be revealed in target cells with lower receptor density. O-glycosylation–deficient CCR5 mutants did not support the entry of viruses pseudotyped with the T-tropic (X4) HXBc2 envelope glycoproteins (data not shown).
The binding of HIV-1 envelope glycoproteins to CCR5 and the entry of R5 viruses into CCR5-expressing cells is greatly influenced by the sulfation of tyrosines 10, 14, and 15 in the CCR5 NH2 terminus (21). Treatment of CCR5-expressing cells with sodium chlorate, an inhibitor of tyrosine sulfation, decreased the binding affinity of the HIV-1 gp120 envelope glycoprotein and ß-chemokines (21). Here, using a mutagenic approach, we provide evidence for the contribution of sulfation of tyrosine 14 in the CCR5 NH2 terminus to the binding of both MIP-1 and RANTES. Although the presence of a phenyl group in the side chain of CCR5 residue 15 contributes to both MIP-1 and RANTES binding, the sulfate moiety on tyrosine 15 appears to be more important for the binding of RANTES than that of MIP-1. Our data are also consistent with a contribution of the tyrosine sulfate at position 10 to MIP-1 binding, although the specific contribution of sulfate was not addressed. Finally, as was previously seen for HIV-1 gp120 binding (21), the tyrosine sulfate at position 3 of CCR5 makes little contribution to chemokine binding.
Together, our results demonstrate a significant role of posttranslational modification of the CCR5 NH2 terminus in binding the natural chemokine ligands. Sialylated O-linked oligosaccharides and sulfated tyrosines provide an array of negative charges on a potentially flexible substructure, allowing electrostatic interactions with the structurally diverse, basic surfaces of different chemokines. High-affinity binding must, in addition, require more specific contacts between the chemokine and the CCR5 sulfotyrosines and sialic acids; this conclusion follows from the observation that acidic amino acid residues cannot effectively substitute for these moieties. A potential ß-turn involving proline 8 on CCR5 may bring the O-glycans attached to serine 6 into proximity with the tyrosine sulfate–rich stretch at residues 10–15, facilitating such specific contacts. The NH2 termini of several chemokine receptors are rich not only in tyrosines that can be potentially sulfated (21), but also in serines and threonines. This suggests that post-translational modifications by sulfate and O-linked oligosaccharides may be common among the chemokine receptors and play roles in ligand binding similar to those demonstrated for CCR5.
Striking parallels exist between the structures implicated in chemokine binding by CCR5 and those contributing to selectin-mediated intercellular adhesion. Sialyl lewis X structures on core 2 branched O-linked oligosaccharides, together with the sulfation of closely located amino-terminal tyrosines, provide the basis for specific interaction of some type of selectin ligands with their counter-receptors. For example, PSGL-1 (P-selectin glycoprotein ligand-1) contains three tyrosines close to the NH2-terminal mucin-like glycosylation site. Sulfation of one of these tyrosines in addition to the sialyl lewis X glycan(s) is essential for P-selectin binding (46–49). In this case, the position, structure, and chirality of the O-linked carbohydrate can influence the affinity of the interaction (49–52).
All - and ß-chemokines, including MIP-1, MIP-1ß, and RANTES, bind sulfated glycosaminoglycans (53, 54). These less specific electrostatic associations may serve to concentrate the chemokines near the target cell surface, setting the stage for more specific interactions with the chemokine receptor. It is possible that the properties of individual chemokines may similarly impact binding to both glycosaminoglycans and chemokine receptors. In this context, it is interesting that Ali and colleagues reported that MIP-1, but not MIP-1ß, bound to CCR5-expressing cells much more efficiently when glycosaminoglycans were present on the cell surface (55). This might reflect some of the differences that we observed in the impact of O-glycosylation on MIP-1 and MIP-1ß binding. Additional work should further elucidate the molecular interactions that allow chemokines to exert their effects on diverse targets.
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Acknowledgments |
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This work was supported by grants from the National Institutes of Health AI41851 and by a Center for AIDS Research grant AI28691. Additional support was provided by the G. Harold and Leila Y. Mathers Foundation, the late William F. McCarty-Cooper, the Friends 10, and Douglas and Judith Krupp. N. Bannert was supported by a fellowship from the Deutsche Forschungsgemeinschaft (DFG).
Submitted: July 26, 2001
Revised: September 27, 2001
Accepted: October 22, 2001
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