Carbohydrate Binding Mechanism of the Macrophage Galactose-type C-type Lectin 1 Revealed by Saturation Transfer Experiments*

Macrophage galactose-type C-type lectins 1 and 2 (MGL1/2) are expressed on the surfaces of macrophages and immature dendritic cells. Despite the high similarity between the primary sequences of MGL1 and MGL2, they display different ligand specificities. MGL1 shows high affinity for the LewisX trisaccharide, whereas MGL2 shows affinity for N-acetylgalactosamine. To elucidate the structural basis for the ligand specificities of the MGLs, we performed NMR analyses of the MGL1-LewisX complex. To identify the LewisX binding site on MGL1, a saturation transfer experiment for the MGL1-LewisX complex where sugar-CH/CH2-selective saturation was applied was carried out. To obtain sugar moiety-specific information on the interface between MGL1 and the LewisX trisaccharide, saturation transfer experiments where each of galactose-H5-, fucose-CH3-, and N-acetylglucosamine-CH3-selective saturations was applied to the MGL1-LewisX complex were performed. Based on these results, we present a LewisX binding mode on MGL1 where the galactose moiety is bound to the primary sugar binding site, including Asp-94, Trp-96, and Asp-118, and the fucose moiety interacts with the secondary sugar binding site, including Ala-89 and Thr-111. Ala-89 and Thr-111 in MGL1 are replaced with arginine and serine in MGL2, respectively. The hydrophobic environment formed by a small side chain of Ala-89 and a methyl group of Thr-111 is a requisite for the accommodation of the fucose moiety of the LewisX trisaccharide within the sugar binding site of MGL1.

Macrophage galactose (Gal) 2 -type calcium-type (C-type) lectins (MGLs; CD301) are carbohydrate recognition proteins expressed on the surfaces of macrophages and immature dendritic cells in humans and rodents (1)(2)(3)(4). In mice, two closely related MGLs, MGL1 and MGL2 (CD301a and CD301b), have been found (3), whereas humans have a single MGL (CD301) gene (2). MGLs have unique carbohydrate specificities toward galactose and N-acetylgalactosamine as monosaccharides, whereas many other C-type lectins on macrophages and dendritic cells have the mannose (Man)-type specificity, such as DC-SIGN and the macrophage mannose receptor (5). The cells expressing MGL1 are widely distributed in connective tissues (6). A variety of biological functions of MGL1 have been reported so far, such as the recognition and endocytosis of glycoproteins with terminal Gal/GalNAc moieties (7,8), contribution to defense against tumor cell metastasis (9,10), and clearance of apoptotic cells in embryos (11,12). MGL2 is also expressed on the cells that display the same distribution pattern as MGL1-positive cells (3). For human MGL, additional functions, involvements in the regulation of effector T cells (13) and the promotion of filovirus entry (14), have been reported.
The MGL molecules are ϳ42-kDa type II transmembrane glycoproteins, which possess a cytoplasmic domain, a transmembrane domain, a neck domain, and a carbohydrate recognition domain (CRD) within each molecule (1,3). Two potential N-glycosylation sites are present in the neck domain. MGL1 and MGL2 share a high amino acid sequence homology (92% for the intact sequence and 80% for the CRD). Both MGL1 and MGL2 have the "QPD" sequences characteristic of the Gal-type C-type lectins in their CRDs (15). Nevertheless MGL1 and MGL2 display different carbohydrate specificities. MGL1 preferentially binds the Lewis X trisaccharides (Gal␤1-4[Fuc␣1-3]GlcNAc), whereas MGL2 exhibits specificity for ␣and ␤-GalNAc (3). A site-directed mutagenesis study revealed that amino acid residues at positions 61, 89, 111, and 125 are implicated in the carbohydrate specificities of MGLs (16). Models of the complexes between MGLs and GalNAc were also constructed using a commercially available docking software without any experimental restraints (16). Therefore, the polysaccharide binding mechanism on MGL1 is putative. To elucidate exact roles of these residues in the sugar binding, structural information for the interaction between MGLs and their ligand carbohydrates is required.
Crystallographic studies on engineered Gal-type mutants of mannose-binding protein complexed with Gal-type monosaccharides have provided insights into the galactose binding modes of these lectins (17)(18)(19). These structures revealed the monosaccharide binding mode but not the polysaccharide binding mode. The crystal structure of human asialoglycoprotein receptor (ASGPR) has also been reported (20). In this structure, no bound sugar is visible even though the protein was co-crystallized with ligand carbohydrate. Therefore, there is no information about the interaction between the ligand and the lectin. In addition, a crystal structure of mouse scavenger receptor C-type lectin (mSRCL) has been solved with bound Lewis X trisaccharide (21). This structure revealed that the Lewis X binding mode is different from that on Man-type lectins, such as DC-SIGN (22). However, the orientation of the indole ring of Trp-698 in mSRCL, which plays a key role in the interaction with the galactose, is ϳ180°different from that of typical Gal-type C-type lectins, such as ASGPR. This is because mSRCL lacks the glycine-rich loop, which is a characteristic structural component of Gal-type lectins, including MGLs and ASGPRs, and plays a crucial role in fixing the correct position of the indole ring of the tryptophan residue to interact with the galactose (17). Although x-ray studies have been extensively performed, little is known about the structural basis of the difference in the ligand binding specificities between MGL1 and MGL2.
In this report, we describe the results of our structural analyses of the MGL1-Lewis X complex to understand the molecular basis for its carbohydrate specificity. First we quantitatively compared the affinities between MGL1 and its sugar ligands, the Lewis X trisaccharide and ␤-methylgalactose, by isothermal calorimetry. Second we analyzed the 13 C chemical shifts originating from MGL1 to characterize its topology. Finally we performed saturation transfer experiments to determine the sugar binding site on MGL1. Based on the structural data, we discuss the differential ligand specificities between MGL1 and MGL2.

Sample Preparation-Recombinant MGL1 was expressed in
Escherichia coli BL21-Codon Plus (DE3)-RP cells (Stratagene) using the pET-21a plasmid containing the CRD of MGL1 (3). The C5S mutation was introduced into the CRD of MGL1, according to the QuikChange site-directed mutagenesis protocol (Stratagene), to prevent intermolecular oligomerization. In the following, we refer to MGL1 with the C5S mutation as the wild-type MGL1 unless otherwise described. Uniformly 15 Nlabeled and 13 C, 15 N-labeled proteins were overexpressed in M9 minimal medium containing 1 g/liter 15 NH 4 Cl (Shoko Co., Ltd.) and 4 g/liter glucose or 2 g/liter [ 13 C]glucose (Cambridge Isotope Laboratories, Inc.), respectively. The cells were fermented at 37°C until the A 600 reached 0.5. Expression was induced with 1 mM isopropyl 1-thio-␤-D-galactopyranoside for 5 h. The uniformly 2 H, 15 15 N-labeled CELTONE (Spectra Stable Isotopes). The cells were fermented at 37°C until the A 600 reached 0.8. Expression was induced with 1 mM isopropyl 1-thio-␤-D-galactopyranoside for 16 h. The expressed MGL1 was refolded and purified as described previously (3). Further purification by size exclusion chromatography on a Superose 12 column or anion exchange chromatography on a Resource Q column (GE Healthcare) was performed after the previous protocols.
The expression vectors for the A89L, A89R, and T111S mutants of MGL1 were prepared using the plasmid of the wildtype MGL1. The mutant proteins were prepared using the same protocol.
Isothermal Titration Calorimetry-Binding of the carbohydrates (the Lewis X trisaccharide and ␤-methylgalactose) to MGL1 (wild type, A89L mutant, A89R mutant, and T111S mutant) was measured by isothermal titration calorimetry (ITC) using a MicroCal VP-ITC MicroCalorimeter (MicroCal Inc.). MGL1 was dialyzed against a buffer containing 10 mM HEPES (pH 7.4), 2 mM CaCl 2 , and 50 mM NaCl. The lyophilized Lewis X trisaccharide (Calbiochem) or ␤-methylgalactose (NBS Biologicals Ltd.) was dissolved in the same buffer used for the dialysis of MGL1. The experiments were performed at 25°C. The sample cell was loaded with the MGL1 solution, and the protein was titrated with the sugar solution. The concentration of the samples were as follows: 0.21 mM wild-type MGL1 was titrated with 1.9 mM Lewis X trisaccharide, 0.48 mM wild-type MGL1 was titrated with 4.9 mM ␤-methylgalactose, 0.37 mM A89L mutant of MGL1 was titrated with 2.8 mM Lewis X trisaccharide, 0.39 mM A89R mutant of MGL1 was titrated with 2.8 mM Lewis X trisaccharide, and 0.20 mM T111S mutant of MGL1 was titrated with 2.9 mM Lewis X trisaccharide. The concentration of MGL1 was determined by measuring the A 280 and the calculated extinction coefficient (23). The concentrations of the carbohydrates were determined by comparing the integrated NMR signal area with that of an internal standard. A total of 29 automatic injections of 10 l each were carried out with spacing delays of 240 s between each injection. The heats of dilution, determined by the titration of the sugar into the same buffer alone, were subtracted from the raw titration data before data analysis. The integrated heats derived from the injection series were fitted to a single site model by the Origin software, which yielded the molar enthalpy of the association and the association constant. The stoichiometry was also estimated in the analyses.
The secondary structure was analyzed by calculating the deviations of the observed 13 C ␣ and 13 C ␤ chemical shifts from their residue-dependent random coil values (⌬C ␣ and ⌬C ␤ ) (30). To account for the possible contributions of the two residues (ith Ϫ 1 and ith ϩ 1 positions) in the sequence flanking the ith position, the parameter ]/4 was used to predict the secondary structural elements (31). The regions with four or more consecutive Ͼ1.4 and ϽϪ1.4 ⌬C ␣,␤ values were predicted as ␣ helices and ␤ strands, respectively.
The saturation transfer experiments were performed at 15°C on a Bruker Avance 600 spectrometer using uniformly 2 H, 15 Nlabeled MGL1 complexed with the Lewis X trisaccharide dissolved in 20% H 2 O, 80% 2 H 2 O (pH 7.5) containing 2 mM CaCl 2 and 50 mM NaCl. The concentrations of MGL1 and the Lewis X trisaccharide were 1.1 and 1.3 mM, respectively. The irradiations were centered at 3.7, 1.1, 0.81, and 1.7 ppm for the saturations of sugar-CH/CH 2 , Gal-H5, Fuc-CH 3 , and GlcNAc-CH 3 , respectively. Band-selective saturations of the sugar-CH/CH 2 resonances were achieved by a train of Gaussian pulse cascades (Q3), each 40 ms long with a maximum ␥B 1 field of 83 Hz. Band-selective saturations of the Gal-H5, Fuc-CH 3 , and Glc-NAc-CH 3 resonances were achieved by a contiguous wave with a ␥B 1 field of 23 Hz. The saturation was followed by the HSQC pulse sequence (32) to detect the amide resonances.
The saturation time used was 2.5 s, and the relaxation delay was set to 2.0 s.
Tertiary Structure Modeling of MGL1-A tertiary structure model of MGL1 was built using the first approach mode of the SWISS-MODEL program server (33). The structure of the CRD of the H1 subunit of ASGPR (Protein Data Bank code 1DV8) was used as a template because of its high amino acid sequence homology to MGL1 (66%). The amino acid residues from Cys-6 to Lys-133 were modeled.

RESULTS
Carbohydrate Binding Activity of Recombinant MGL1-To characterize the carbohydrate binding activity of MGL1 quantitatively, the association constants for the interactions between wild-type MGL1 and the Lewis X trisaccharide, wildtype MGL1 and ␤-methylgalactose, the A89L mutant of MGL1 and the Lewis X trisaccharide, the A89R mutant of MGL1 and the Lewis X trisaccharide, and the T111S mutant of MGL1 and the Lewis X trisaccharide were determined by ITC. Fig. 1 shows the titration curves for the Lewis X (A) and ␤-methylgalactose (B) binding to wild-type MGL1. The results obtained from the experiments are given in Table 1. Wild-type MGL1 showed higher affinity to the Lewis X trisaccharide compared     with that to ␤-methylgalactose. The A89L, A89R, and T111S mutants showed decreased affinity to the Lewis X trisaccharide compared with that of the wild-type MGL1. It was also found that the sugar binding site within the CRD of MGL1 was single. The association constants obtained from ITC in the present study are different from those from SPR in the previous study (16). The difference is because of the immobilization effects in the SPR experiments as described previously (34,35). In the previous SPR experiments, the rebinding effects were not negligible because the total amount of the sugar ligand immobi-lized on the sensor chip via polyacrylamide was high. However, what occurs in the SPR experiments under the condition with the high contents of the sugar ligands is quite similar to that on cell surfaces. In this sense, the data from the SPR experiments is meaningful. In this study, to prepare NMR samples of the MGL1-Lewis X complex in a proper stoichiometry, the association constants were determined by ITC under the same condition as that for the NMR experiments. Secondary Structural Elements and Topology of MGL1-The 66% sequence homology is high for MGL1 assuming the similar CRD folding. However, there are still possibilities of subtle structural differences between MGL1 and its model in partial unfolding of ␣ helices, the positions of short helices, and the length of ␤ strands. To rule out these possibilities, we analyzed the secondary structural elements and topology of the MGL1-Lewis X complex using NMR. Fig. 2 shows the 1 H-15 N HSQC spectrum of the MGL1-Lewis X complex. The backbone resonance assignments for the complex were accomplished by analyzing a set of the standard triple resonance NMR spectra (HNCA, HN(CO)CA, HNCACB, and CBCA(CO)NH). Of 131 possible resonances originating from the backbone amide groups within the CRD of MGL1, 128 resonances (98%) could be assigned. Complete (137 of 137) assignments were obtained for the 13 C ␣ and 13 C ␤ resonances. Using the deviations of the 13 C ␣ and 13 C ␤ chemical shifts from the random coil values (⌬ 13 C ␣,␤ ), the secondary structural elements within MGL1 were analyzed (Fig.  3A). The configurations of the ␤ sheets were determined by analyzing the interstrand NOEs among the main chain protons. The resonances originating from the H ␣ were assigned by analyzing the HBHA(CO)NH spectrum. The predicted topology of the secondary structure of MGL1 is shown in Fig. 3B. MGL1 consists of two ␣ helices (residues 27-36 and 48 -59) and three ␤ sheets (sheets I, II, and III). Sheet I consists of three ␤ strands (␤1, residues 16 -19; ␤3, residues 39 -43; and ␤9, residues 129 -133), whereas sheet II has two ␤ strands (␤2, residues 22-26; and ␤7, residues 124 -126), and sheet III has four ␤ strands (␤4, residues 61-64; ␤5,  residues 105-111; ␤6, residues 116 -120; and ␤8, residues 126 -129). As for the two regions comprising residues 2-5 and 85-88, no interstrand NOEs were observed, suggesting that no ␤ sheet structure exists in these regions, although the chemical shift predicted the ␤ strand-like conformation. Based on the similarities in the amino acid sequence and the topology of the secondary structure, the structural model of MGL1 was constructed by SWISS-MODEL (Fig. 3C).
Lewis X Binding Site on MGL1 Determined by Saturation Transfer Experiments-To determine the binding site of the Lewis X trisaccharide on MGL1, saturation transfer experiments (36 -38) were performed on MGL1 complexed with the Lewis X trisaccharide. We first checked the effect of the saturation on MGL1 in the free state. Each of the saturations at 3.7, 1.1, 0.81, and 1.7 ppm caused no obvious signal intensity reductions for the amide resonances because the protein had been fully deuterated. Exceptionally signal intensity reduction ratios from 0.1 to 0.2 were observed for Glu-37, Asn-38, Ser-39, and Val-44 by the saturation at 3.7 ppm probably because of the spin diffusion from nearby hydroxyl protons, such as those of Tyr-13 and Ser-39.
The Lewis X -selective saturation was achieved by applying an rf irradiation centered at 3.7 ppm, which corresponds to most of the CH/CH 2 protons within the sugar in the MGL1-bound state. Fig. 4 shows an expanded region of the 1 H-15 N HSQC spectra of the MGL1-Lewis X complex with and without the saturation. Residue-selective signal intensity reductions were observed at 15°C. Few signal intensity reductions were observed at 25°C because of the short rotational correlation time of the MGL1-Lewis X complex. It might be effective to lower the experimental temperature for the saturation transfer experiment on a complex with a molecular weight of ϳ20,000. Of 127 analyzed signals originating from the main chain amide groups of MGL1, the signals from Gln-92, Asp-94, Trp-96, and Asp-118 exhibited intensity reduction ratios of more than 0.3; the signals from Ala-89, His-109, Trp-116, and Asn-117 showed intensity reduction ratios from 0.15 to 0.3; and the signals from Phe-97, Gly-98, Asp-106, Cys-107, Thr-111, and Asp-119 showed intensity reduction ratios from 0.1 to 0.15 (Fig. 5A).
The residues affected by the saturation were mapped on the model structure of MGL1 (Fig. 6A). The affected residues formed a contiguous surface on MGL1, indicating that these residues form the Lewis X binding site (Fig. 6D).
To obtain the sugar moiety-specific information on the interface between MGL1 and the Lewis X trisaccharide, saturation transfer experiments, where the H5 proton of the Gal moiety (Gal-H5), the methyl protons of the Fuc moiety (Fuc-CH 3 ), and the methyl protons of the GlcNAc moiety (GlcNAc-CH 3 ) were saturated, were performed. The selective saturations of Gal-H5, Fuc-CH 3 , and GlcNAc-CH 3 in the MGL1-bound state were achieved by applying rf irradiations centered at 1.1, 0.81, and 1.7 ppm, respectively. The resonances originating from the Lewis X trisaccharide in the MGL1-bound state were assigned by analyzing the double quantum-filtered correlation spectroscopy, total correlation spectroscopy, and NOE spectroscopy spectra of the Lewis X trisaccharide complexed with 2 H, 15 N-labeled MGL1. By the Gal-H5 saturation, the signals from Asp-94, Trp-96, and Asp-118 showed intensity reduction ratios from 0.15 to 0.3, and the signals from Ala-89, Gln-92, His-109, and Asn-117 showed intensity reduction ratios from 0.1 to 0.15 (Fig. 5B). The affected residues were mapped on the model structure of MGL1 (Fig. 6B). By the Fuc-CH 3 saturation, the signals from Ala-89, Gln-92, Asp-94, Trp-116, Asn-117, and Asp-118 showed intensity reduction ratios from 0.15 to 0.3, and the signals from Trp-96, His-109, and Thr-111 showed intensity reduction ratios from 0.1 to 0.15 (Fig. 5C). The affected residues were also mapped on the model structure of MGL1 (Fig. 6C). The GlcNAc-CH 3 saturation slightly affected the intensity of the signal from Trp-96 (Fig. 5D).

DISCUSSION
The topology of MGL1 predicted by the NMR analyses indicated that the CRD of MGL1 basically adopts the typical C-type lectin fold, which characteristically has two ␣ helices and two antiparallel ␤ sheets within the fold (39). In addition, the topology of MGL1 was almost identical to that of the x-ray crystal structure of the human ASGPR, which shares high (66%) amino acid sequence homology to MGL1 (20). The secondary structural elements observed within the model structure that was made using SWISS-MODEL (Fig. 3C) agreed well with those predicted by the NMR analyses, supporting the validity of the main chain configuration of the modeled structure. In the following discussion, we use the modeled structure of MGL1 to interpret the results.
The Lewis X binding site on MGL1 was successfully determined by the saturation transfer experiment where the CH/CH 2 protons within the Lewis X trisaccharide were saturated (Fig. 6, A and D)  site is mainly composed of polar residues, Gln-92, Asp-94, Asn-117, and Asp-118. The polar region is sandwiched by two hydrophobic regions. One region is composed of Trp-96, Phe-97, and Gly-98, and the other region is formed by Ala-89, Thr-111, and Trp-116.
Among the residues in the Lewis X binding site, three residues, Asp-94, Trp-96, and Asp-118, experienced signal intensity reductions of more than 0.15 by the Gal-H5-selective saturation (Fig. 6B). The duration of 2.5 s used for the selective saturation is long enough to cause intra-Gal spin diffusion. Therefore, the residues affected by the Gal-H5-selective saturation are in close proximity to the protons within the Gal moiety. By the Fuc-CH 3 -selective saturation, six residues, Ala-89, Gln-92, Asp-94, Trp-116, Asn-117, and Asp-118 experienced signal intensity reductions of more than 0.15 (Fig.  6C). These residues are in close proximity to the protons within the Fuc moiety. In contrast, no residues experienced signal intensity reductions of more than 0.15 by the Glc-NAc-CH 3 -selective saturation. This result suggests that the GlcNAc moiety of the Lewis X trisaccharide does not make direct interactions with MGL1. This observation is supported by the fact that the sum of the residues affected by the Gal-H5 saturation and those affected by the Fuc-CH 3 saturation corresponded to that of the residues constituting the Lewis X binding site. In addition, few chemical shift perturbations were observed for resonances originating from the GlcNAc moiety in the Lewis X trisaccharide upon the MGL1 binding (data not shown). Weak signal intensity reduction of Trp-96 by the saturation of GlcNAc-CH 3 (1.7 ppm) will be caused by incidental saturation of the H6 proton of the Gal moiety (1.9 ppm).
In total, the Gal and Fuc moieties of the Lewis X trisaccharide occupy the entire Lewis X binding site on MGL1. The Gal moiety is located in close proximity to Asp-94, Trp-96, and Asp-118. The Fuc moiety binding site is located adjacent to the Gal

Carbohydrate Binding Mechanism of MGL1
moiety binding site and includes Ala-89 and Thr-111. On the other hand, the GlcNAc moiety makes no direct contact with MGL1 but is located over the Gal and Fuc rings. The putative Lewis X binding mode on MGL1 is illustrated in Fig. 7.
In the crystal structures of the Gal-type mannose-binding protein mutants complexed with Gal-type monosaccharides, the galactose ring is bound on the calcium ion, which is chelated by five residues, corresponding to Gln-92, Asp-94, Glu-105, Asp-118, and Asn-117 in MGL1. The tryptophan residue, corresponding to Trp-96 in MGL1, packs against the apolar face of the galactose ring, and the amide group of the aspartic acid residue, corresponding to Asp-118 in MGL1, is located near the 2-CH of the galactose (17)(18)(19). These arrangements are consistent with the present results of the saturation transfer experiments with the MGL1-Lewis X complex. Interestingly the overall Lewis X binding mode on MGL1 is highly related with that on mSRCL (21). However, amino acid residues interacting with the Fuc moiety of the Lewis X trisaccharide are not conserved between these lectins, and the orientation of the tryptophan side chain of mSRCL (Trp-698), which interacts with the galac-tose moiety of the Lewis X trisaccharide, is different from those of typical Gal-type C-type lectins with the glycine-rich loop (17)(18)(19)(20). These structural differences might explain the 4.3 times higher affinity of MGL1 for the Lewis X trisaccharide than that of human scavenger receptor C-type lectin (40). Fig. 8 compares the amino acid sequences of MGL1, MGL2, and the related Gal-type C-type lectins. Although most of the amino acid residues identified within the Lewis X binding site on MGL1 are conserved in MGL2, interestingly Ala-89 and Thr-111 are replaced by Arg-89 and Ser-111 in MGL2, respectively. This observation suggests that the amino acid residues at positions 89 and 111 are responsible for the different ligand specificities between MGL1 and MGL2. As for MGL1, the side chain of Ala-89 is small enough to accommodate the Fuc moiety of the Lewis X trisaccharide within the secondary sugar binding site around Ala-89. On the other hand, the bulky side chain of Arg-89 in MGL2 would sterically hinder the access of the Fuc moiety, leading to lower affinity for the Lewis X trisaccharide. This consideration is supported by the site-directed mutagenesis study where the A89L and A89R mutants of MGL1 showed lower affinity (Ͻ10%) for the Lewis X trisaccharide as compared with that of the wild type. The importance of the methyl group of Thr-111 for the binding to the Lewis X trisaccharide was also confirmed by the site-directed mutagenesis study. The hydrophobic environment formed by a small side chain of Ala-89 and a methyl group of Thr-111 is a requisite for the accommodation of the Fuc moiety of the Lewis X trisaccharide within the sugar binding site of MGL1.
There is a 6-fold difference in the affinity of MGL1 for the Lewis X trisaccharide versus ␤-methylgalactose. This difference corresponds to ϳ1 kcal/mol at 25°C. Based on the NMR results, we suggest that MGL1 will form two more van der Waals interactions with the Lewis X trisaccharide compared with ␤-methylgalactose: one between the methyl group of fucose and the methyl group of Ala-89 and the other between the methyl group of fucose and the methyl group of Thr-111. In each experiment, the irradiation was applied at 3.7 ppm (CH/CH 2 protons within the Lewis X trisaccharide) (A), 1.1 ppm (Gal-H5 within the Lewis X trisaccharide) (B), 0.8 ppm (Fuc-CH 3 within the Lewis X trisaccharide) (C), and 1.7 ppm (GlcNAc-CH 3 within the Lewis X trisaccharide) (D). The residues that displayed reduction ratios of more than 0.1 are labeled. The error bars were calculated using the formula I sat Ϯ I noise(sat) I ref ϯ I noise(ref) Ϫ I sat I ref where I noise(sat) and I noise(ref) represent the noise intensity in the spectra with and without saturation, respectively. The ϳ1 kcal/mol binding free energy can be explained by two van der Waals interactions (41).
In MGLs and hepatic lectins, two types of amino acids can be found at the position corresponding to Ala-89 in MGL1 (Fig. 8). One type has alanine residues at this position (A-type), whereas the other type has arginine/lysine residues (RK-type). The amino acid residue at position 89 plays a role in the accommodation of the Lewis X -type branched oligosaccharide (A-type) or a role not to accommodate it (RK-type). Recently Coombs et al. (42) reported that rat MGL, with A-type sequence, displayed high affinity for oligosaccharides with terminal Lewis X moiety, and rat hepatic lectin-1, with R-type sequence, bound strongly to oligosaccharides with terminal GalNAc. These observations agree with our interpretation on the ligand specificities of the Gal-type C-type lectins. The fact that only a few amino acid residues are responsible for the carbohydrate specificity of the Gal-type C-type lectin suggests that it might be possible to design lectins with other carbohydrate specificities in rational manners. An interesting unsolved question of animal lectins is how animal lectins show different specificities although they have similar structures. Our finding of the key residues to determine the specificity is useful for understanding recognition modes of C-type lectins and will contribute the structural basis of the interaction between lectins and their ligands.