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Volume 17, Number 13, Issue of July 1, 1997 pp. 5038-5045
Copyright ©1997 Society for Neuroscience

Tyrosine Phosphorylation of Nicotinic Acetylcholine Receptor Mediates Grb2 Binding

Marcie Colledge and Stanley C. Froehner

Department of Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599

ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
FOOTNOTES
REFERENCES

ABSTRACT

Tyrosine phosphorylation of the nicotinic acetylcholine receptor (AChR) is associated with an altered rate of receptor desensitization and also may play a role in agrin-induced receptor clustering. We have demonstrated a previously unsuspected interaction between Torpedo AChR and the adaptor protein Grb2. The binding is mediated by the Src homology 2 (SH2) domain of Grb2 and the tyrosine-phosphorylated delta  subunit of the AChR. Dephosphorylation of the delta  subunit abolishes Grb2 binding. A cytoplasmic domain of the delta  subunit contains a binding motif (pYXNX) for the SH2 domain of Grb2. Indeed, a phosphopeptide corresponding to this region of the delta  subunit binds to Grb2 SH2 fusion proteins with relatively high affinity, whereas a peptide lacking phosphorylation on tyrosine exhibits no binding. Grb2 is colocalized with the AChR on the innervated face of Torpedo electrocytes. Furthermore, Grb2 specifically copurifies with AChR solubilized from postsynaptic membranes. These data suggest a novel role for tyrosine phosphorylation of the AChR in the initiation of a Grb2-mediated signaling cascade at the postsynaptic membrane.

Key words: acetylcholine receptor; tyrosine phosphorylation; Grb2; SH2 domain; postsynaptic specialization; signal transduction

INTRODUCTION

Tyrosine phosphorylation is a critical event in the transduction of signals in many cell types. This reversible post-translational modification often functions to trigger the assembly of transient protein-protein complexes. The identification of protein-binding modules that specifically recognize phosphotyrosine has led to the characterization of downstream effectors of tyrosine kinases. The Src homology 2 (SH2) domain (Koch et al., 1991) and the more recently identified protein tyrosine binding (PTB) domain (Blaikie et al., 1994; Kavanaugh and Williams, 1994) each recognize phosphotyrosine in the context of a specific sequence of amino acids (Songyang et al., 1993, 1995b; Kavanaugh et al., 1995). These domains are found in diverse intracellular signaling molecules, including protein kinases and phosphatases, as well as modular adaptor proteins. The latter proteins, which include Shc, p85, and Grb2, lack any apparent enzymatic activity but are composed almost entirely of multiple protein-binding domains (Pawson, 1995). Thus, recruitment of adaptor proteins to tyrosine-phosphorylated proteins provides a scaffold on which signal transduction components can be assembled (for review, see Cohen et al., 1995; Pawson, 1995).

Ligand-driven dimerization of growth factor receptors leads to autophosphorylation of the receptor on tyrosine residues, creating a high-affinity docking site for SH2 domain-containing proteins (for review, see Ullrich and Schlessinger, 1990; Heldin, 1995). The adaptor protein Grb2 is composed of a central SH2 domain flanked by two Src homology 3 (SH3) domains (Lowenstein et al., 1992). In the cytoplasm of unstimulated cells Grb2 is complexed via its two SH3 domains, with the Sos (son of sevenless) protein. On receptor activation, the complex is recruited to the cell membrane via the SH2 domain of Grb2, bringing Sos to the cellular location of its substrate protein Ras. Sos, a guanine-nucleotide exchange factor, converts Ras from its inactive GDP-bound state to its active GTP-bound state, leading to the activation of Ras-dependent signaling pathways (for review, see Schlessinger, 1993, 1994).

The identification of ion channels, including potassium channels (Lev et al., 1995; Holmes et al., 1996), NMDA receptors (Moon et al., 1994; Wang and Salter, 1994; Lau and Huganir, 1995), and nicotinic acetylcholine receptors (AChRs) (Huganir et al., 1984; Qu et al., 1990), as substrates for tyrosine kinases suggests that this modification may play an important role in the regulation of synaptic function throughout the nervous system. The bulk of our knowledge about the functional consequences of tyrosine phosphorylation of ion channels comes from studies of the AChR at the neuromuscular junction (NMJ) and its homologous synapse in the electric organ of Torpedo. The AChR is a ligand-gated ion channel, composed of four homologous subunits in the stoichiometry alpha 2beta gamma delta , arranged around a central ion pore. Each subunit spans the membrane four times, with both N and C termini extending extracellularly (Galzi et al., 1991; Chavez and Hall, 1992). A large cytoplasmic loop between transmembrane domains three and four contains consensus sites for phosphorylation by multiple kinases (for review, see Swope et al., 1992). A single tyrosine residue in this region of the beta , gamma , and delta  subunits of Torpedo AChR is phosphorylated by endogenous kinase activity in the postsynaptic membrane (Huganir et al., 1984; Wagner et al., 1991). Phosphorylation of the AChR by both serine and tyrosine kinases is associated with an increased rate of receptor desensitization (Huganir et al., 1986; Hopfield et al., 1988). In addition, agrin-induced tyrosine phosphorylation of the AChR may play a role in its clustering to high densities in the postsynaptic membrane of the neuromuscular junction (Qu et al., 1990; Wallace et al., 1991; Qu and Huganir, 1994; Wallace, 1994; Ferns et al., 1996).

In this study we provide evidence for an adaptor protein, Grb2, binding to the AChR, a ligand-gated ion channel. We show high-affinity binding between the SH2 domain of Grb2 and the phosphotyrosine site of the delta  subunit of the AChR. The two proteins are colocalized on the innervated face of the electrocyte; furthermore, Grb2 specifically copurifies with the AChR solubilized from Torpedo postsynaptic membranes. Together these data demonstrate an association between the AChR and Grb2, which suggests a role for the AChR in initiating a signal transduction pathway involved in the assembly or maintenance of specializations at the synapse.

MATERIALS AND METHODS

Preparation of Torpedo membranes and isolation of AChR. Frozen Torpedo nobiliana electric organ was obtained from Biofish (Georgetown, MA). AChR-rich membranes were isolated as previously described (Porter and Froehner, 1983) with the omission of the second sucrose gradient step. This omission has negligible effect on the purity of the preparation. Iodoacetamide and N-ethylmaleimide also were omitted from all solutions. For isolation of AChR, membranes (2 mg/ml) were solubilized by incubation on ice for 30 min in extraction buffer [1% Triton X-100, 150 mM NaCl, and 10 mM phosphate, pH 7.4, including protease (Kramarcy et al., 1994) and phosphatase inhibitors (Lamphere and Lienhard, 1992)]. Insoluble material was removed by centrifugation at 40,000 × g for 30 min at 4°C. AChRs were isolated by incubating the supernatant with alpha -bungarotoxin coupled to CNBr-activated Sepharose 4B (Sigma, St. Louis, MO) for 2 hr at 4°C. As a control for specificity of binding to the resin, an equivalent sample of supernatant was incubated with excess alpha -bungarotoxin (25 µM) for 1 hr at 4°C before incubation with the toxin-Sepharose. Beads were washed extensively with extraction buffer and equilibrated in the same buffer without detergent. Bound proteins were eluted with SDS sample buffer.

Dephosphorylation of Torpedo membrane proteins. Torpedo postsynaptic membranes (100 µg) were diluted 10-fold in phosphatase buffer (10 mM MgCl2, 10 mM ZnCl2, and 100 mM glycine, pH 10.4) and centrifuged at 40,000 × g for 30 min at 4°C. The pellet was resuspended in 200 µl of phosphatase buffer containing 0.1% Triton X-100 to increase accessibility to the intravesicular compartment. Calf intestinal alkaline phosphatase (20 U; Pierce, Rockford, IL) was added to one-half of the sample (100 µl) and incubated at 30°C for 2 hr. The reaction was stopped by the addition of SDS sample buffer. The second half of the sample was treated identically but with the omission of enzyme. Equivalent amounts (5 µg) of phosphatase-treated and untreated Torpedo membrane proteins were resolved by SDS-PAGE, transferred to nitrocellulose, and analyzed by protein overlay assay and immunoblotting.

Protein overlay assay and immunoblotting. Proteins of Torpedo postsynaptic membranes or subunits of purified AChR were separated on 9% SDS gels and transferred to nitrocellulose membranes. Nitrocellulose blots were incubated for 1 hr in blocking buffer (5% milk, 0.1% Tween 20, 150 mM NaCl, and 100 mM Tris, pH 7.5). Protein overlay assays were performed by using glutathione S-transferase (GST) fusion proteins of mouse Grb2 (GST-Grb2, amino acids 1-217) or individual domains of Grb2 (GST-Grb2 N-SH3, amino acids 1-68; GST-Grb2 SH2, amino acids 54-164; GST-Grb2 C-SH3, amino acids 156-199) (Santa Cruz Biotechnology, Santa Cruz, CA). Nitrocellulose membrane strips were incubated with GST fusion proteins (200 nM) in overlay buffer containing 3% BSA and (in mM) 150 NaCl, 2 MgCl2, 1 dithiothreitol, and 20 HEPES, pH 7.5, overnight at 4°C. Bound fusion proteins were detected with anti-GST monoclonal antibodies (mAb; 1:1000; Santa Cruz Biotechnology). Parallel membrane strips were analyzed by Western blotting with mAb 88B (90 pM) (Froehner et al., 1983), which recognizes both the gamma  and delta  subunits of the AChR or anti-phosphotyrosine mAb, 4G10 (1 µg/ml; Upstate Biotechnology, Lake Placid, NY), or PY20 (1 µg/ml; Transduction Laboratories, Lexington, KY). Grb2 was identified by immunoblotting with an anti-Grb2 mAb (1:4000; Transduction Laboratories). All primary antibody incubations were followed by incubation with horseradish peroxidase-conjugated secondary antibodies (1:3000; Jackson ImmunoResearch, West Grove, PA), and immunoreactive bands were visualized with enhanced chemiluminescence substrate (ECL; Pierce).

Immunofluorescence and confocal microscopy. Cryosections (6 µm) of fixed Narcine brasiliensis electric organ were incubated in blocking buffer (1% fish gelatin and 1% BSA in PBS, pH 7.3) containing BODIPY FL-conjugated alpha -bungarotoxin (1:300; Molecular Probes, Eugene, OR) and rabbit anti-Grb2 antibodies (1:100; Santa Cruz Biotechnology), followed by incubation with Texas Red-conjugated anti-rabbit antibodies (1:200; Jackson ImmunoResearch). Digital images were acquired via a Leica TCS 4D confocal microscope.

Preparation of Grb2 SH2 fusion proteins. A GST fusion protein cDNA construct (pGEX-2t; Pharmacia, Piscataway, NJ) encoding the SH2 domain of Grb2 (amino acids 56-105) was generously provided by Dr. Lawrence Quilliam (Indiana University, IN). Large-scale protein expression in transformed Escherichia coli JM109 cells was induced with 1 mM isopropyl beta -D-thiogalactopyranoside. Cells were lysed by sonication on ice, and fusion proteins were purified on glutathione-Sepharose beads (Pharmacia), followed by elution with 5 mM reduced glutathione. Protein concentration was determined by Bradford assay (Bio-Rad, Hercules, CA). Purified GST-Grb2 SH2 fusion proteins were exchanged into HEPES-buffered saline (HBS; 150 mM NaCl, 3.4 mM EDTA, 0.005% surfactant P20, and 10 mM HEPES, pH 7.4) and used immediately in surface plasmon resonance assays.

Surface plasmon resonance---BIAcore. Surface plasmon resonance was used to determine quantitatively the strength of the interaction between Grb2 SH2 fusion proteins and delta  subunit peptides in real time. This technique has been described in detail previously (Fagerstam, 1991; Johnsson et al., 1991). Biotinylated peptides corresponding to amino acids 388-401 (SKAQEYFNIKSRSE) of the Torpedo AChR delta subunit were synthesized (University of North Carolina Peptide Synthesis Facility) with either tyrosine or phosphotyrosine at position 393. Peptides were immobilized on a streptavidin-coated SA5 flow cell. HBS solutions containing different concentrations of GST-Grb2 SH2 (31.3, 62.5, 125, 250, 500, and 1000 nM) were injected onto the peptide surface, and subsequent binding was measured as an increase in resonance units (RU). The basic method for estimation of association and dissociation rate constants by BIAcore analysis has been described (Karlsson et al., 1991).

RESULTS

Grb2 fusion proteins bind to the delta  subunit of the AChR

Many proteins important for synaptic function have their counterparts in the electric organ of marine rays, a tissue homologous to skeletal muscle. Postsynaptic membranes of this tissue have provided a rich source for the identification and characterization of many synaptic proteins, including rapsyn, syntrophin, and agrin (Sobel et al., 1977; Godfrey et al., 1984; Froehner et al., 1987). To identify potential binding partners for Grb2 in Torpedo postsynaptic membranes, we used a protein overlay assay in which GST fusion proteins were used to probe membrane proteins separated by SDS-PAGE and transferred to nitrocellulose. We consistently observed binding of GST-Grb2 fusion proteins, but not control GST proteins, to several proteins, the approximate molecular weights of which were 150, 130, 90, and 65 kDa (Fig. 1, compare C and D). The most prominent binding was to the 65 kDa band. Parallel immunoblots showed that mAb 88B (which recognizes both the gamma  and delta  subunits of the AChR) labeled the same position, suggesting that this band was the delta subunit of the AChR (Fig. 1A). To confirm that this protein was indeed the AChR delta  subunit and not another protein migrating to the same position, we performed protein overlays on purified AChR, isolated by alpha -bungarotoxin affinity chromatography. The amount of AChR was adjusted to be approximately equivalent to the amount of AChR present in the membrane samples as judged by immunoblotting with mAb 88B (Fig. 1A). Figure 1, C and D, shows that GST-Grb2, but not control GST, binds directly to the 65 kDa delta  subunit of isolated AChR.
Fig. 1. Grb2 binds to the delta  subunit of the AChR. Torpedo postsynaptic membrane proteins (Memb) and isolated AChR subunits (AChR) were separated by SDS-PAGE and transferred to nitrocellulose membranes. A, Immunoblot with mAb 88B indicates the position of the gamma  and delta  AChR subunits. Higher molecular weight bands are aggregates and dimers of the delta  subunit and degradation products thereof. Minor lower molecular weight bands are degradation products of the gamma  and delta  subunits. B, Tyrosine phosphorylation of the beta  and delta  subunits of the AChR is shown by Western blotting, using anti-phosphotyrosine (anti-PY) antibody 4G10. C, Protein overlays with control GST show no binding to membrane proteins or AChR subunits. D, Overlays with GST-Grb2 show binding to a prominent band at 65 kDa, corresponding to the delta  subunit of the AChR. Other bands of 90, 130, and 150 kDa in membrane samples also were observed to bind Grb2. Arrows on the left indicate the position of the beta , gamma , and delta  AChR subunits; numbers on the right indicate positions of molecular weight markers (in kDa).
[View Larger Version of this Image (56K GIF file)]

Grb2-delta subunit binding is mediated by an SH2-phosphotyrosine interaction

Grb2 consists of three protein-binding domains: a central SH2 domain flanked by N- and C-terminal SH3 domains. SH3 domains bind proline-rich sequences, whereas SH2 domains recognize phosphotyrosine motifs (for review, see Chardin et al., 1995). Examination of intracellular domain sequences of the delta  subunit did not reveal any consensus sites for SH3 binding. Moreover, the AChR delta  subunit is endogenously tyrosine-phosphorylated in our Torpedo membrane preparations (Fig. 1B), suggesting that the binding of Grb2 to the delta  subunit could be mediated by the SH2 domain of Grb2. To test this hypothesis, we used fusion proteins corresponding to the three individual domains of Grb2 in overlay assays on isolated Torpedo AChR. As shown in Figure 2A, fusion proteins containing only the SH2 domain of Grb2, but neither of the SH3 domains, bind to the delta  subunit of the AChR.
Fig. 2. Grb2-delta subunit binding is mediated by an SH2-phosphotyrosine interaction. A, Isolated Torpedo AChR subunits were resolved by SDS-PAGE, transferred to nitrocellulose, and subjected to protein overlay analysis. Full-length GST-Grb2 (FL) binds to the delta  subunit, as shown in Figure 1. No binding is observed with either SH3 domain fusion protein of Grb2 (N-SH3 and C-SH3). Fusion proteins containing the SH2 domain (SH2), however, bind to the delta  subunit. B, Equivalent amounts of Torpedo membranes (5 µg) treated with (right lane) and without (left lane) alkaline phosphatase were subjected to SDS-PAGE and transferred to nitrocellulose for protein overlay analysis. Panel A, Immunoblot with mAb 88B shows that approximately equal amounts of delta  subunit protein were loaded for each condition. Panel B, Parallel immunoblots, using a cocktail of anti-phosphotyrosine (anti-PY) antibodies, 4G10 and PY20, indicate an absence of immunoreactivity in the phosphatase-treated membranes. Panel C, Protein overlays with control GST show no binding. Panel D, Binding of full-length GST-Grb2 to the delta  subunit is abolished by phosphatase treatment. Binding to the 90 and 150 kDa bands is retained.
[View Larger Version of this Image (50K GIF file)]

To test the specificity of the SH2-mediated interaction, we took advantage of the fact that three prominent Torpedo membrane proteins are tyrosine-phosphorylated by endogenous kinase(s): the beta  and delta  subunits of the AChR (50 and 65 kDa) and dystrobrevin (an 87 kDa protein related to dystrophin) (Wagner et al., 1991, 1993). Phosphotyrosine immunoblots of our postsynaptic membrane preparations identify the AChR beta  and delta  subunits and an 87 kDa band, which we presume to be dystrobrevin. We typically observe an additional phosphotyrosine protein at 130 kDa, which may correspond to dimers of the delta  subunit because this band also is recognized by mAb 88B (Figs. 1B, 2B, panel B). Phosphotyrosine was removed from membrane proteins by treatment with alkaline phosphatase, and dephosphorylated proteins were reassayed for Grb2 binding activity in overlay assays. Although an equivalent amount of delta subunit protein was present (Fig. 2B, panel A), the removal of phosphotyrosine (Fig. 2B, panel B) abolished the ability of GST-Grb2 to bind to the 65 kDa delta  subunit in the alkaline phosphatase-treated sample (Fig. 2B, panel D). Binding to the 90 and 150 kDa bands was retained, suggesting that these proteins may interact with the SH3 domain(s) of Grb2. Furthermore, although the beta  subunit is phosphorylated to a level comparable to the delta  subunit, we observed no binding to Grb2 fusion proteins (Figs. 1, 2). Thus the beta  subunit provides a negative internal control in our overlay assays, further supporting the specificity of the Grb2 SH2-delta subunit association. Together these results indicate that Grb2 and the AChR delta  subunit associate in vitro via an SH2 domain-phosphotyrosine-mediated interaction.

A delta  subunit phosphopeptide binds to the SH2 domain of Grb2

The specificity of recognition of phosphotyrosine peptides by different SH2 domains is determined by the amino acid sequence immediately carboxyl to the phosphotyrosine (pY) residue (Songyang et al., 1993). Phosphopeptide library analysis predicts the optimal binding motif for the SH2 domain of Grb2 to be pYXNX (X is any amino acid) (Songyang et al., 1994). The sequence that follows the phosphotyrosine site in the cytoplasmic loop of the delta  subunit (pY393FNI) is a precise consensus for Grb2 SH2 binding, whereas sequences in homologous regions of the beta  and gamma  subunits do not conform to the Grb2 SH2 consensus motif (Fig. 3). This is in agreement with the finding that the tyrosine-phosphorylated beta  subunit does not bind Grb2 in overlay assays (see Figs. 1, 2).
Fig. 3. Tyrosine phosphorylation sites of Torpedo AChR subunits. Alignment of tyrosine phosphorylation sites in the large cytoplasmic loop of Torpedo beta , gamma , and delta  subunits reveals a Grb2 SH2 consensus motif in the delta  subunit, but not in the beta  or gamma  subunits. The pY+2 position is boxed and shaded. The phosphotyrosine is indicated with an arrow.
[View Larger Version of this Image (17K GIF file)]

We used surface plasmon resonance to assay quantitatively the binding between the SH2 domain of Grb2 and peptides corresponding to the phosphotyrosine consensus site of the delta  subunit. This approach, which allows real-time measurement of binding kinetics and affinities, has been used previously to study interactions between different SH2 domains and tyrosine autophosphorylation sites of growth factor receptors (Felder et al., 1993; Panayotou et al., 1993; Lombardo et al., 1995). Tyrosine-phosphorylated peptides (pY393) corresponding to amino acids 388-401 of the Torpedo delta  subunit were coupled to one cell of a sensor chip. Control peptides, containing tyrosine instead of phosphotyrosine at position 393, were coupled to a second cell. Several concentrations of Grb2 SH2 fusion proteins (31.3-1000 nM) were injected onto the sensor chip surface. Figure 4A displays typical "sensorgrams" for binding of different concentrations of Grb2 SH2 fusion proteins to immobilized delta  subunit peptide. Robust, relatively rapid binding of the SH2 domain to the tyrosine-phosphorylated peptide was observed. We found no binding to the nonphosphorylated peptide, even at the highest fusion protein concentration tested (1000 nM). In addition, control GST did not interact with the phosphorylated peptide (data not shown). Extrapolated steady-state binding responses were plotted as a function of fusion protein concentration (Fig. 4B). The dissociation constant (Kd) was estimated to be 226 nM by curve fitting, using nonlinear regression analysis. Thus, the SH2 domain of Grb2 binds to a tyrosine-phosphorylated peptide of the Torpedo delta  subunit specifically and with relatively high affinity.

Fig. 4. Interaction of the SH2 domain of Grb2 with a tyrosine-phosphorylated delta  subunit peptide. A, Raw binding data. Resonance signal (RU) is plotted as a function of time for several concentrations of GST-Grb2 SH2 injected onto the flow cell. Binding of fusion proteins to immobilized phosphorylated (solid line) and nonphosphorylated (broken line) delta  subunit peptide is shown. Concentrations of fusion proteins injected were 31.3, 62.5, 125, 250, 500, and 1000 nM. B, Determination of dissociation constant. Extrapolated steady-state binding responses (Req) are plotted versus fusion protein concentration. A dissociation constant (Kd) of 226 nM was estimated by nonlinear regression analysis.
[View Larger Version of this Image (24K GIF file)]

Grb2 binds to the AChR in Torpedo membranes

Our biochemical data demonstrate that Grb2 and the AChR delta  subunit are capable of direct association in vitro. As a first step toward determining whether they interact in vivo, AChR-rich electric organ membranes were immunoblotted with antibodies specific for Grb2. A protein of the appropriate size (25 kDa) was identified in the membranes by two different antibodies (data not shown), indicating that Grb2 is indeed a component of isolated postsynaptic membranes. However, the presence of Grb2 in our postsynaptic membrane preparations did not rule out the possibility that it was a contaminant derived from the noninnervated membrane of the electrocyte. To address this concern, we used confocal microscopy to investigate the subcellular localization of Grb2 relative to AChR in Narcine electroplax. Narcine electroplax are very similar to Torpedo but are better suited to immunofluorescence studies. As previously described (Sealock and Kavookjian, 1980), AChRs are restricted to the innervated face of the electrocyte (Fig. 5, top). Grb2 showed a strikingly similar pattern of labeling in these cells (Fig. 5, middle). In fact, merging the two images (Fig. 5, bottom) indicated that Grb2 is localized in precise register with the AChR on the innervated face of the electrocyte.
Fig. 5. Grb2 and AChR are colocalized in electric organ postsynaptic membranes. Frozen Narcine electric organ sections (6 µm) were labeled simultaneously for AChR with alpha -bungarotoxin (top, green) and Grb2 (middle, red), processed for immunofluorescence, and analyzed by confocal microscopy. Grb2 antibodies label the innervated face of the electrocyte, in precise register with the AChR (bottom, merged image).
[View Larger Version of this Image (92K GIF file)]

To address whether the two molecules form a complex in the cell, we asked whether Grb2 copurifies with AChR. To this end, postsynaptic membranes were extracted in 1% Triton X-100 and AChR isolated by alpha -bungarotoxin beads. Bound proteins were eluted with SDS-sample buffer and analyzed by immunoblotting with antibodies specific for Grb2. As shown in Figure 6, Grb2 specifically copurifies with the AChR. When binding of AChR to the beads was blocked by preincubation of solubilized membranes with excess toxin, Grb2 was not retained, indicating that the binding of Grb2 specifically depends on the presence of AChR on the beads. Although AChR subunits are easily detected by Coomassie staining, we did not observe a band corresponding in size to Grb2 in the AChR preparation (Fig. 6, left). Thus, at least under these purification conditions, the stoichiometry of Grb2 to AChR is low. This observation is not inconsistent with the signaling role of Grb2. Linking a small percentage of tyrosine-phosphorylated AChR to downstream enzymatic pathways likely would be sufficient to activate a signaling cascade. It is also possible that the association between the AChR and Grb2 may be disrupted partially under the purification conditions that we used. Thus, although a small proportion of AChR seems to be associated with Grb2 under these circumstances, the interaction is nevertheless significant. These results suggest that Grb2 and the delta  subunit of the nicotinic AChR associate in vivo.

Fig. 6. Grb2 associates with the AChR in situ. AChRs were isolated from solubilized Torpedo membranes by alpha -bungarotoxin-Sepharose, were eluted in SDS, and were resolved by SDS-PAGE. Coomassie staining of the preparation shows the four subunits of the AChR: alpha , ~40 kDa; beta , ~50 kDa; gamma , ~60 kDa; and delta , ~65 kDa. Preincubation with excess alpha -bungarotoxin (25 µM) prevents binding of AChR to the toxin-Sepharose (left). Immunoblotting the samples with anti-Grb2 antibodies reveals that Grb2 specifically copurifies with the AChR (right).
[View Larger Version of this Image (61K GIF file)]

DISCUSSION

We have identified a previously unsuspected interaction between the tyrosine-phosphorylated AChR and the SH2 domain of Grb2. Several lines of evidence support the specificity of this association. Protein overlay assays demonstrate that GST fusion proteins of Grb2, but not control GST proteins, directly bind to the AChR delta  subunit in Torpedo postsynaptic membranes. Fusion proteins containing only the SH2 domain of Grb2, but neither of the SH3 domains, bind to the delta  subunit. Dephosphorylation of the delta  subunit completely abolishes Grb2 binding. Although the beta  subunit of the AChR also is tyrosine-phosphorylated in our membrane preparations, we observed no interaction with Grb2 in overlay assays. The Torpedo delta  subunit contains a precise motif (pYXNX) for recognition by the SH2 domain of Grb2 that is not present in homologous regions of the beta  or gamma  subunits. A phosphotyrosine peptide corresponding to this region of the delta  subunit interacts with Grb2 SH2 fusion proteins with relatively high affinity, whereas a peptide lacking phosphorylation on tyrosine exhibits no binding. Thus, we have narrowed the binding site for Grb2 to within 14 amino acids surrounding the site of tyrosine phosphorylation in the long intracellular loop of the delta  subunit. Furthermore, we have demonstrated that Grb2 has a subcellular distribution identical to that of the AChR in the electrocyte; both molecules are concentrated at and restricted to the innervated membrane. Finally, isolation of the AChR from solubilized electric organ results in the specific copurification of Grb2, indicating that the two molecules form a complex in situ.

A clue to the function of this association may come from identification of SH3 binding partners for Grb2 in the postsynaptic membrane. One possibility is suggested by the recent finding that Grb2 can bind, via its SH3 domain(s), to a proline-rich region of beta -dystroglycan (Yang et al., 1995). beta -Dystroglycan is a component of the dystrophin-glycoprotein complex, serving as a transmembrane link between the extracellular peripheral membrane protein alpha -dystroglycan and cytoskeletal dystrophin or utrophin (Ibraghimov-Beskrovnaya et al., 1992). Recently, alpha -dystroglycan was identified as a cell surface binding site for agrin (Bowe et al., 1994; Campanelli et al., 1994; Gee et al., 1994; Sugiyama et al., 1994). This finding has focused much attention on the possible role of the dystrophin-protein complex in mediating the AChR clustering effects of agrin. If AChR-bound Grb2 were also to bind beta -dystroglycan via its SH3 domains, Grb2 could provide a direct link between the AChR and the dystrophin/utrophin protein complex. However, we have found no evidence for an interaction between Grb2 and beta -dystroglycan in our studies. Although we confirmed, by Western blotting, the presence of beta -dystroglycan in our Torpedo membrane preparations (Bowe et al., 1994) (data not shown), we observed no binding of Grb2 to a protein corresponding in size to beta -dystroglycan (43 kDa) in overlay assays (see Fig. 1D). In addition, in affinity purification experiments, we did not observe copurification of beta -dystroglycan with complexes containing the AChR and Grb2 (data not shown). Ruling out technical or species differences, we cannot explain the apparent discrepancy between our results and those of Yang et al. (1995) at this time. Interestingly, we observed binding of Grb2 to proteins of 90 and 150 kDa in our overlay assays (see Fig. 1) that did not depend on phosphorylation (see Fig. 2B, panel D). Future studies will address whether these may represent SH3 binding partners for Grb2 at the synapse.

One important question is whether the association between Grb2 and the AChR occurs in mammals, particularly at the NMJ. Alignment of delta  subunit amino acid sequences from different species reveals that the asparagine in the pY+2 position, which is important for recognition by the SH2 domain of Grb2, is not conserved. Mammalian delta  subunit orthologs contain a serine in this position. Yet the preference for hydrophobic amino acids at the pY+1 and +3 positions (Song-yang et al., 1994) is conserved in mammals (mouse, pYFSL). Whether serine can substitute for asparagine in the Grb2 SH2 binding site is not known. Certainly, in vitro peptide library analysis indicates a strong preference for asparagine in this position (Songyang et al., 1994). Association between phosphorylated mouse delta  subunit peptides and Grb2 SH2 fusion proteins was not detected in preliminary surface plasmon resonance assays (data not shown), suggesting that the affinity of the interaction, if it occurs at all, is low. It is interesting to consider whether a low-affinity interaction would be sufficient to mediate signaling at the mammalian endplate, where the density of AChR approaches 10,000 per square micron. This high local concentration may compensate for a weak interaction between Grb2 and the mammalian delta  subunit and, in fact, may necessitate low-affinity interactions for rapid onset and termination of signaling. In addition, it was reported recently that the Grb2-Sos complex binds phosphopeptides with higher affinity than Grb2 alone (Chook et al., 1996). This raises the possibility that the functional in vivo binding partner for the AChR may be Grb2 complexed with Sos or another protein such as beta -dystroglycan. Thus, although the sequence surrounding the mammalian tyrosine phosphorylation site is less than optimal for Grb2 binding, it still may be an important mediator of transmembrane signaling.

Identification of upstream tyrosine kinase pathways, especially those mediating delta  subunit phosphorylation, may provide insight into the function of the association of Grb2 with the AChR. One synaptic molecule implicated in the activation of a tyrosine kinase pathway is agrin. This nerve-derived protein originally was isolated for its striking ability to cause AChR aggregation in chick myotubes (Godfrey et al., 1984). The observation that agrin induces tyrosine phosphorylation of the beta  (Wallace et al., 1991; Qu and Huganir, 1994; Wallace, 1994; Ferns et al., 1996), and perhaps the delta  (Qu and Huganir, 1994), subunit of the AChR has led to the hypothesis that this is a critical, and perhaps a prerequisite, step in the AChR clustering pathway. A recently identified muscle-specific receptor tyrosine kinase, MuSK, has been shown to be essential for NMJ formation (Valenzuela et al., 1995; DeChiara et al., 1996). Indeed, MuSK can be activated by agrin and is a component of the receptor complex for agrin (Glass et al., 1996). Activation of MuSK results specifically in tyrosine phosphorylation of the beta , but not the delta , subunit of the AChR in vitro (Gillespie et al., 1996; Glass et al., 1996), suggesting that it does not catalyze delta  subunit phosphorylation in vivo.

Tyrosine kinases of the Src family have been identified in association with the AChR. In electric organ, coimmunoprecipitation experiments demonstrated that tyrosine-phosphorylated AChRs are complexed with Fyn and a novel member of this family, Fyk (Swope and Huganir, 1993). The binding seems to be mediated by the SH2 domains of the kinases and the delta  subunit of the AChR (Swope and Huganir, 1994). This raises the possibility that the SH2 domains of Fyn and Fyk may compete with Grb2 for binding to the delta  subunit. However, this idea is contrary to recent studies that suggest that specificity in tyrosine kinase signaling may result, in part, from the ability of different SH2 domains to distinguish among different target sequences (Songyang et al., 1993). The optimal sequence for binding to Fyn SH2 domains is pYEEI, as compared with the optimal Grb2 SH2 binding site of pYXNX (Songyang et al., 1994). The delta  subunit phosphotyrosine site of pYFNI is a precise motif for Grb2 SH2 binding, whereas only the isoleucine in the third position is consistent with recognition by the SH2 domain of Fyn. Whether the delta  subunit interacts with various SH2 domain-containing proteins remains to be resolved. Regardless, the delta  subunit does not seem to be a substrate of Fyn and Fyk, because their binding to the AChR requires tyrosine phosphorylation.

An interaction between Src and the mammalian AChR recently has been reported (Fuhrer and Hall, 1996). The binding seems to be mediated by an N-terminal unique region of the kinase and the intracellular loop of the beta  subunit. Src was able to tyrosine phosphorylate beta  subunit fusion proteins in vitro. AChRs, affinity-purified from mouse myotubes, were associated with both Src and Fyn and contained tyrosine-phosphorylated beta  subunit. There was no evidence for Src association with, or phosphorylation of, the delta  subunit in these studies. Thus, it is not likely that Src family kinases catalyze delta  subunit phosphorylation.

Although the kinase responsible for tyrosine phosphorylation of the delta  subunit remains a mystery, it is interesting to note that the amino acid sequence preceding Y393 of the delta  subunit forms a consensus motif for phosphorylation by members of the receptor tyrosine kinase family (Songyang et al., 1995a). An intriguing possibility is that the ARIA/erbB receptor tyrosine kinase pathway may be involved. ARIA (acetylcholine receptor-inducing activity) originally was isolated from chick brain extracts for its ability to promote the synthesis of AChR subunits in aneural myotubes (Jessell et al., 1979). Induction of AChR gene expression by ARIA recently was shown to require activation of the MAP kinase and PI3 kinase pathways via the erbB receptors (Si et al., 1996; Tansey et al., 1996). The model predicts that ARIA may bind to an erbB2/erbB3 heterodimer and in doing so may activate the Ras/MAP kinase pathway through erbB2 and the PI3 kinase pathway through erbB3 (Tansey et al., 1996). One possibility is that ARIA stimulation of erbB2 may lead to AChR phosphorylation, recruiting Grb2 to the postsynaptic membrane via its SH2 domain. In turn, this could lead to activation of the Ras/MAP kinase signal transduction pathway, ultimately inducing AChR subunit gene expression.

FOOTNOTES

Received Feb. 10, 1997; revised April 8, 1997; accepted April 14, 1997.

  

This work was supported by a grant (to S.C.F.) from the National Institutes of Health and a fellowship (to M.C.) from the Natural Sciences and Engineering Research Council of Canada. We thank Drs. Neal Kramarcy and Robert Sealock (University of North Carolina) for assistance with confocal microscopy and Dr. Chris Lombardo (Macromolecular Interactions Facility, University of North Carolina) for assistance with collection and analysis of BIAcore data. We thank Dr. Lawrence Quilliam (Indiana University) for supplying the cDNA for Grb2 SH2. We are grateful to Drs. Channing Der, Brian Kay, John O'Bryan, and Michael Schaller (University of North Carolina) for helpful discussions and to Drs. Sharon Milgram (University of North Carolina) and Robert Sealock for critically reading this manuscript.

Correspondence should be addressed to Dr. Stanley C. Froehner, Department of Physiology, Room 266 MSRB, Campus Box 7545, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599. 


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