Snake venom galactoside-binding lectins: a structural and functional overview
© Sartim and Sampaio. 2015
Received: 29 December 2014
Accepted: 16 September 2015
Published: 24 September 2015
Snake venom galactoside-binding lectins (SVgalLs) comprise a class of toxins capable of recognizing and interacting with terminal galactoside residues of glycans. In the past 35 years, since the first report on the purification of thrombolectin from Bothrops atrox snake venom, several SVgalLs from Viperidae and Elapidae snake families have been described, as has progressive improvement in the investigation of structural/functional aspects of these lectins. Moreover, the advances of techniques applied in protein-carbohydrate recognition have provided important approaches in order to screen for possible biological targets. The present review describes the efforts over the past 35 years to elucidate SVgalLs, highlighting their structure and carbohydrate recognition function involved in envenomation pathophysiology and potential biomedical applications.
KeywordsSnake venom C-type lectin Galactoside-binding protein Carbohydrate recognition domain Glycoconjugates Inflammatory response Antitumor activity Bactericidal activity Mitogenic activity Platelet aggregation
Lectins are non-enzyme and non-immune proteins capable of binding reversibly, specifically and non-covalently to carbohydrates, and have been isolated from plants, microorganisms and animal sources . Although distinct lectins lack primary structural similarity, they share similar glycan-binding specificities in which the carbohydrate recognition domain (CRD—represented by a segment of limited amino acid residues within the lectin) is responsible for the glycan-interaction activity [2, 3].
Among animal sources, calcium dependent (C-type) lectins have been identified in snake venoms and are classified into two distinct groups: the true C-type glycan-binding lectins; and C-type lectin-like proteins. The C-type lectin-like (also named “snaclecs” from snake venom C-type lectins ) are heterodimeric proteins with CRD-related lectin-like domain that are not capable of interacting specifically with sugars . On the other hand, the glycan-binding C-type lectins are homodimeric proteins, composed of two identical disulfide-linked polypeptide monomers with molecular mass of approximately 15 kDa, presenting a functional CRD that binds to carbohydrates and are capable of inducing hemagglutination by recognizing erythrocyte surface glycoconjugates .
The first studies on snake venom lectins were reported by Flexner and Noguchi  wherein the authors observed agglutination activity of erythrocytes and leukocytes by a variety of venoms. However, the first data on the isolation of a snake venom lectin was reported by Gartner et al.  almost 80 years later, describing the purification and characterization of thrombolectin, the first galactoside-binding lectin isolated from Bothrops atrox. Since then, several reports on purification and both the structural and functional characterization of snake venom lectins have been described from the snake families Viperidae and Elapidae, including from the genera Bothrops, Crotalus, Bitis, Agkistrodon, Lachesis, Dendroaspis and Trimeresurus. Most snake venom glycan-binding lectins are members of the C-type galactoside-binding proteins due to their ability to interact with terminal galactoside residues in a calcium-dependent manner [8–21]. The lectin isolated from Lachesis muta stenophrys (LmL) was first classified as lectin-like by the authors . However, taking into account its molecular and functional aspects (which will be further discussed in this review), a more appropriate definition was provided by classifying it as a true galactose-binding lectin.
The present review aims to introduce the efforts over the past 35 years on the study of snake venom galactoside-binding C-type lectins (SVgalLs) by providing insights on the structural and biological activities associated with its glycan recognition pattern.
Molecular structure analysis
Important advances in molecular analysis and structure determination of SVgalLs have been performed during the past years. Although the detail of structural information on these lectins varies from a single SDS-PAGE molecular mass analysis to a complete quaternary structure determination, overall molecular aspects indicate a high similarity among these proteins as will be discussed in this section. Currently, rattlesnake lectin (RSL), from Crotalus atrox venom, is the only SVgalL whose complete structure was determined by X-ray crystallography , and is widely applied in structural analysis comparisons with others lectins from this class .
All SVgalLs are homodimeric proteins composed of disulfide-linked monomers presenting molecular mass varying from 14 to 16.2 kDa. The primary structures of 12 SVgalLs were determined, and presented from 134 to 136 amino acid residues as described for the following lectins: RSL—rattlesnake lectin from Crotalus atrox , ApL—Agkistrodon piscivorus piscivorus lectin , BaL—Bitis arietans lectin , CrL—Crotalus ruber lectin , BiL—Bothrops insularis lectin , BmLec—Bothrops moojeni lectin , BpalL—Bothrops pauloensis lectin , BJcuL—Bothrops jararacussu lectin , BpirL—Bothrops pirajai lectin , LmL—Lachesis muta stenophrys lectin , ToL—Trimeresurus okinavensis lectin  and TsL—Trimeresurus stejnegeri lectin . Amino acid sequence analysis among the referenced SVgalLs using BLAST searching tool  showed an identity degree from 82 to 97 % among them, indicating a high primary structural similarity within these lectins.
In general, C-type galactoside-binding lectins CRD motifs are represented by three amino acid residues, Gln-Pro-Asp, which are considered to be determinants of their galactose specificities, where this carbohydrate interaction is mediated by calcium ions . As shown in Fig. 1, this motif is fully conserved within all SVgalLs with primary structure determined, indicating its common carbohydrate recognition activity. As observed in the RSL structure complexed with lactose in Fig. 2b, the CRD is responsible for coordinating the calcium ion by interacting with the residues Q96, D98, E104, N119 and D120. The interaction with galactose residue from lactose (a disaccharide composed of galatose-glucose) occurs by coordination of galactose hydroxyl groups at position 3 and 4 of the hexose ring with the calcium ion (Fig. 2b) and by direct hydrogen bonds to residues Q96, D98, E104 and N119. Furthermore, the residue Q121 is involved in water-mediated hydrogen bond coordination of the 2-hydroxyl group of the galactose moiety, while residue Y100 also interacts with the galactose ring .
The aspects involving the galactose binding specificity of lectins are related to the hydrogen-bond interaction of residues Q96 and D98 with the galactose 3 and 4-hydroxyl groups, as observed in RSL , differently from mannose binding protein in which CRD is composed of an EPN motif (glutamic acid, proline and asparagine), whereas interaction with mannose 3-OH involves coordination of the calcium ion and simultaneous hydrogen bonding to residues E and N . Aside from its CRD responsible for galactose binding activity mediated by calcium ion, RSL shows an alternative ion binding site that coordinates a sodium ion by residues Y15, S42, and Q132 and a water molecule, (Fig. 2a) . This ion binding site is thought to be important in stabilizing RSL conformation , where the presence of these amino acids is fully conserved in the other SVgalLs and might also have an effect on these lectins (Fig. 1).
It has been reported that SVgalLs are capable of forming high-order oligomers [22, 33]. The X-ray crystallography structure of RSL reveals a decameric protein composed of five disulfide-linked dimers (ten monomers in total) arranged as two pseudo-5-fold symmetric pentamers as shown in Fig. 2c. As in the case of RSL, evaluation of BJcuL quaternary structure using different computational methods and biophysical experiments such as small-angle X-ray light scattering, revealed that the lectin, in solution, is a globular protein with molecular mass of 147.5 kDa with indications that BJcuL also forms an oligomerized decameric structure .
The decameric complex of RSL is composed of five dimers (Cys86–Cys86 disulfide-linked monomers) arranged as two pentamers (Fig. 2c), where its oligomeric structure is mainly maintained by four salt bridges and apolar interactions . The fact that the RSL decameric structure presents ten carbohydrate-binding sites located on the edge of the two pentamers strongly suggests that the lectin presents a multivalent capacity of ligand-binding activity, as shown by its ability to induce erythrocyte agglutination due to cross-linking with the opposing cell surface. The ability to mediate multivalent interactions with different biological glycoconjugates have been described for others SVgalLs, such as galatrox, from Bothrops atrox snake venom, which induces a pro-inflammatory activity through its interaction with galactose-bearing glycoconjugates on the surface of neutrophils and macrophages and extracellular matrix (ECM) proteins .
Given the effect of lectins on biological functions, understanding the molecular basis of carbohydrate recognition pattern comprises a relevant issue in lectinomics [35, 36]. So far, with the exception of the mannose-binding lectin isolated from Oxyuranus scutellatus crude venom , most snake venom glycan-binding lectins present the ability to interact specifically with sugars via terminal galactoside residues . Interestingly, this similarity of galactose recognition patterns is reflected in several aspects among SVgalLs, such as the purification procedure which, for most snake lectins, is performed by single step liquid chromatography using affinity resins with a matrix composed of lactose- or galactose-based components [8–21, 38–41].
Carbohydrate inhibition specificity of SVgalLs
Terminal galactoside carbohydrates (inhibition order)
Akgistrodon piscivorus piscivorus 
D-galactose > Lactose > N-acetyl-D-galactosamine
Bothrops atrox 
Thiodigalactoside > Lactose > Methyl β-D-galactopyranoside > Methyl α-D-galactopyranoside > D-galactose
Bothrops insularis 
Thiodigalactoside > Lactose > D-galactose > N-acetyl-D-galactosamine
Bothrops jararaca 
Thiodigalactoside > Lactose = N-acetyl-lactosamine > Methyl β-D-galactoside = D-galactose > Methyl α-D-galactoside > N-acetyl-D-galactosamine
Akgistrodon piscivorus leukostoma 
Thiodigalactoside > Lactose > Methyl β-D-galactopyranoside > D-galactose >
Bothrops jararacussu 
Lactose > D-galactose > D-galactosamine
Crotalus atrox 
Thiodigalactoside > Lactose > Methyl β-D-galactopyranoside = D-galactose >
Bothrops leucurus 
D-galactose > Lactose > N-acetyl-D-glucosamine > asialofetuin
Bothrops pauloensis 
Lactose > D-galactose > N-acetyl-D-galactosamine
Bothrops pirajai 
Lactose > D-galactose
Akgistrodon contortrix contortrix 
Thiodigalactoside > Methyl β-D-galactopyranoside > Lactose > Methyl α-D-galactopyranoside > D-galactose
Crotalus ruber 
Thiodigalactoside > N-acetyl-D-galactosamine = Lactulose > Lactose =
Methyl β-D-galactoside > D-galactose
Lachesis muta stenophyrs 
Thiodigalactoside > Lactose > Methyl β D-galactopyranoside > D-galactose >
Methyl α D-galactopyranoside > Galactosamine
Trimeresurus okinavensis 
Thiodigalactoside = Lactose
Dendroaspis jamesonii 
Thiodigalactoside = Lactose > Methyl α D-galactoside > Metyl β D-galactoside > D-galactose > Galactosamine
Glycans are found in living systems as free oligosaccharides or as glycoconjugates present on the cell surface and ECM, and are involved in a broad spectrum of biological functions including the signaling, recognition and adhesion of molecules [1, 36, 44]. The recognition of specific glycans by lectins represents a key event in a variety of biological phenomena involving cell-cell and cell-ECM component interactions, as observed in cell migration, apoptosis, immunomodulation and inflammation, host pathogen interactions and mitogenic induction [1, 45].
The SVgalLs comprise a group of exogenous glycan binding proteins (GBP) that have been reported to mediate several biological functions associated with snake envenomation pathophysiology and other biological properties [8, 11, 13, 34, 46–49]. The present section will approach functional features of SVgalLs and the association of their carbohydrate recognition specificity in these activities.
In addition to hemagglutination activity, the ability of lectins to stimulate lymphocytes to undergo mitosis has been described from the early 1960s . Since then, several other lectins from different sources have been reported to induce cell mitogenisis through recognition of sugars on the cell surface leading to signal transmission .
Subsequent to the early reports on biological characterization of SVgalLs, authors have assessed their ability to induce mitogenic activity. Mastro et al. , in a study working with five different SVgalLs, have shown that RSL, cottonmouth lectin (CML—isolated from Akgistrodon piscivorus leukostoma venom) and Dendroaspis jamesonii lectin (Jameson’s mamba lectin—JML) were capable of stimulating lymphocytes to undergo DNA synthesis, unlike thrombolectin and copperhead lectin (CuHL—isolated from Akgistrodon contortrix contortrix venom). The authors also showed that lymphocyte mitogenic activity of CML was preferentially induced in T-cells rather than B-cells, and was mediated by its carbohydrate binding properties. Moreover, CML macrophages stimulation increased lymphocyte proliferation presumably by involving interleukin-1 production from macrophages .
Other SVgalLs have also been assessed for their mitogenic activity, in which ToL was described as inducing the proliferation of human peripheral lymphocytes, mouse macrophages and bovine arterial endothelial cells . On the other hand, Bothrops godmani Lectin (BgL) induced no mitogenic activity in human peripheral blood mononuclear cells . The variation observed in the mitogenic activity among SVgalLs may be associated with the carbohydrate-binding specificity of these lectins, associated with a glycosylation pattern of cell surface receptors that are involved in this phenomenon .
Investigations into the involvement of SVgalLs in the hemostasis system evidenced that these lectins act exclusively on platelet functions, as shown by the platelet aggregation agonists BmLec , RSL , Agkistrodon piscivorus leukostoma lectin (AplLec ), ToL  and LmL . The proposed mechanism of platelet activation was based on the report of Ogilvie et al. , which showed that LmL recognizes glycans on the platelet surface and induces platelet aggregation mediated by glycoprotein IIb/IIIa signaling. Therefore, considering the binding specificity of SVgalLs, these results also indicate the presence of terminal galactoside residues on platelet surface glycoconjugates, where the recognition by the lectins seems to initiate the platelet stimulation and possibly induce blood coagulation disorders associated with snakebites.
On the other hand, several other lectins were not capable of inducing or inhibiting platelet aggregation, namely CuHL , galatrox , BjL , BJcuL , thrombolectin  and CrL . This functional diversity involving platelet function may be associated with differences in the carbohydrate recognition specificity among SVgalLs .
Several endogenous and exogenous GBPs have been described as playing a pivotal role by regulating the participation of a wide variety of events during inflammation [52–56]. The participation of SVgalLs in inflammatory response has been assessed using different animal models and in vitro approaches in order to evaluate leukocyte involvement and recognition of ECM glycoconjugates in the inflammatory response.
Lomonte et al.  evidenced that BgL was capable of inducing moderate acute phase mouse paw edema that was inhibited by the antihistamine drug cyproheptadine. A similar pattern of acute mouse paw edema was observed in BJcuL, an effect that was associated with an increase in local vascular permeability . Considering that galatrox and LmL were not capable of inducing mouse paw edema [19, 30, 57], the above results indicate that SVgalLs-induced paw edema might be associated with the capacity of the lectins to stimulate resident mast cell degranulation and the release of histamine and/or serotonin in order to trigger local inflammatory response.
In addition to paw edema, investigations concerning different sites of SVgalLs-induced inflammation and the involvement of leukocytes and ECM glycoproteins have been assessed. Elifio-Esposito et al.  demonstrated that BJcuL induced an increase in rolling and adherence of leukocytes observed in cremaster muscle microvessels of mice with topical administration of the lectin. Additionally, the authors also demonstrated that the lectin is capable of binding to the glycoproteins’ fibronectin and vitronectin, assuming that the extravasation of peripheral blood leukocytes into the inflammatory site involves cellular adhesion to ECM proteins mediated by BJcuL . In order to confirm this evidence and elucidate the involvement of neutrophils in BJcuL-induced inflammation, a continuous study by Elifio-Esposito et al.  was performed by applying in vitro approaches. The authors observed that BJcuL not only recognizes glycoligands on the neutrophil cell surface, but also promotes polarization and migration, and enhances adhesion to the ECM components fibronectin and matrigel. The lectin also induced neutrophil functional activation by increasing phagocytosis and superoxide production .
Similar findings were also reported by Sartim et al. , who evaluated the pro-inflammatory response of galatrox. Although the lectin was not capable of inducing paw edema , in mice it was capable of promoting acute neutrophil migration into the peritoneal cavity and the release of cytokines IL-1α and IL-6. Moreover, galatrox was capable of recognizing neutrophil cell membrane glycoconjugates, of interacting with the polylactosamine ECM component laminin, and also inducing neutrophil chemotaxis in vitro . Interestingly, the possible involvement of resident cells on galatrox-induced inflammation was assumed due to the ability of the lectin to stimulate macrophages in vitro to produce the pro-inflammatory mediators IL-6 and TNF-α, and keratinocyte-derived chemokine by interacting and triggering toll-like receptor 4 signaling in an MyD88-dependent pathway .
The above results show that the inflammatory-induced mechanism of the mentioned SVgalLs is characterized by neutrophil influx to the inflammation site promoted by direct lectin-ECM interaction chemoattractive role and/or through stimulation of resident macrophages or mast cells in order to express soluble mediators responsible for amplifying the inflammatory response. An exceeding inflammatory process induced by these lectins, and others venom components, may be associated with snake envenomation pathophysiology related to tissue damage and organ injury [59, 60].
During snake envenomation, renal disorders represents an important clinical manifestation where the kidney represents an organ vulnerable to venom components due to its high degree of vascularization. Multiple factors including hemodynamic changes, inflammatory reactions and nephrotoxic effects of toxins are responsible for several manifestations such as proteinuria, hematuria and renal failure . Studies involving the evaluation of renal disorders induced by SVgalLs in isolated rat kidneys have been reported. The lectins BiL, BpirL and BmLec were capable of inducing alterations in renal functional parameters such as perfusion pressure, renal vascular resistance, urinary flow, glomerular filtration rate and tubular ion transport [17, 24, 48]. Moreover, indomethacin, an anti-inflammatory drug that inhibits lipidic mediator prostaglandin synthesis, completely inhibited all evaluated parameters of renal alterations induced by BmLec . Additionally, histological analysis of kidneys from animals that received BiL suggested direct injury to glomerular and tubular renal cells . Therefore, a rational proposal on the mechanism of renal alterations suggested by the authors indicates a direct cytotoxicity induced by the lectins at the glomerular level and/or the involvement of systemic pro-inflammatory mediators such as prostaglandins, suggesting their involvement in envenomation-induced renal disorders [17, 24, 48].
Other biological functions
As mentioned above, SVgalLs are able to recognize and interact with several biological glycoconjugates in order to induce their functional activity, being associated with snakebite-related pathologies. However, given the advance of emerging techniques applied to determine the carbohydrate composition of glycoconjugates in association with the large amount of data on lectin-glycan recognition, the investigation of novel applications of these snake venom GBPs has been largely completed [1, 36, 43].
Ryanodine receptors are calcium-release channels expressed in several human cells such as those present in sarcoplasmatic reticulum (SR) from skeletal muscle, and are associated with muscle contraction . A wide variety of compounds from diverse natural sources have been assessed as molecular approaches to elucidate the molecular mechanism of calcium-release involving ryanodine receptors. Among these chemical probes, the snake venom lectins ToL and BaL were reported to trigger calcium release specifically from a heavy fraction of skeletal muscle SR (HSR) by interacting with HSR ryanodine receptors, where the binding sites by which both SVgalLs interact appeared to be different from those sites able to recognize the well known agonists caffeine, ryanodine and myotoxin alpha, isolated from Crotalus viridis viridis venom [39, 47]. These findings indicate both lectins as possible novel pharmacological tools for application in functional studies of calcium release from HSR in skeletal muscle.
Considering that during the infection process pathogen adhesion to the host cell involves protein-glycan interactions [63, 64], glycoconjugates from the pathogen cell surface represents a potential target for SVgalLs. Castanheira et al.  showed that BpalL, a lectin isolated from Bothrops pauloensis venom, induced agglutination but not toxicity of promastigote forms of Leishmania amazonesis through interaction with galactoside glycoconjugates on the parasite membrane. The effects of BpalL on bacteria were also evaluated, where the lectin inhibited gram-positive Staphylococcus aureus growth, but not gram-negative E.coli . Similar findings were also obtained for BleucL, isolated from Bothrops leucurus venom, which promoted antibacterial activity against gram-positive bacteria Bacillus subtilis, Staphylococcus aureus and Enterococcus faecalis, but not against gram-negative E. coli or Klebsiella pneumonia . The authors suggested that the difference in susceptibility is associated with the interaction of BpalL and BleucL with peptidoglycan present in the gram-positive bacterium cell wall, while the lectins may not reach the same targets on Gram-negative due to the outer cell wall [20, 21]. In contrast, BmLec, isolated form Bothrops moojeni venom, induced bactericidal activity against gram-negative Xanthomonas axonopodis pv. passiflorae, where ultrastructural analysis showed that the lectin binds to the membrane resulting in the formation of the bacterial aggregates, and also the development of large vesicles in the bacterial cell membrane that lead to membrane rupture . This contrast in relation to the effects to gram-negative bacteria among the mentioned SVgalLs may be associated with the variation of carbohydrate binding specificity of these lectins to outer cell wall glycoconjugates or even to morphological singularities among bacteria .
SVgalL tumoral cell lines citotoxicity
Snake venom specie (reference)
Tumorigenic cell line
Bothrops atrox 
HL-60 (human promyelocytic leukemia)
MDA-MB- 435 (human breast carcinoma); OVCAR-5 (ovarian carcinoma); U87 and A-172 (glioblastoma); MKN45 and AGS (human gastric carcinoma); HT29 (human colon adenocarcinoma)
K562 (human chronic myelocytic leukemia); NCI-H292 (human lung mucoepidermoid carcinoma); Hep-2 (human larynx epidermoid carcinoma); B16-F10 (melanoma)
Moreover, the authors also observed that the lectin increases the permeability of the external mitochondrial membrane and induces respiration decrease . Similar findings on mitochondrial dysfunction were also observed for BleucL toxicity toward the B16-F10 cell line, which induced the increase of calcium concentrations in cytosol and mitochondrial superoxide generation, and favored mitochondrial permeability transition pore opening, leading to cell death by necrosis . Despite its cytotoxicity toward tumor cell lines, BleucL presented no changes in viability of the nontumorigenic HaCaT cells derived from human keratinocytes, indicating a selective death-induced activity towards cancer cells [70, 72]. Aside from cytotoxicity, SVgalLs presented other features involving antitumor activity as evidenced by BJcuL which was capable of inhibiting adhesion of HT29, MKN45 and AGS cell lines to ECM components within matrigel, indicating an important mechanism to annul the attachment of cancer cells to tissue [68, 69]. The abovementioned findings suggest these lectins as potential anticancer agents owing to their abilities to recognize, kill and suppress common features of tumor cell lines during cancer progression.
During the past 35 years, scientists have shown that snake venoms represent an important source of galactoside-binding lectins that are involved in diverse features of snake biology. The specificity towards terminal galactose residues confers to these molecules the ability to recognize a wide variety of glycoconjugates, and act as an important tool in glycan-codified functions. This capacity corroborates these lectins as potential approaches applied in basic research, clinical diagnosis and pharmacological therapy. Therefore, future studies on SVgalLs become crucial not only for the elucidation of their involvement in snake envenomation pathophysiology, but also for the development of biotechnological tools.
The authors would like to thank the State of São Paulo Research Foundation (FAPESP grant n. 2011/23236-4) for their funding of this research. Thanks are also due to the Center for the Study of Venoms and Venomous Animals (CEVAP) of UNESP for enabling the publication of this special collection (CNPq process 469660/2014-7).
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- Ghazarian H, Idoni B, Oppenheimer SB. A glycobiology review: carbohydrates, lectins and implications in cancer therapeutics. Acta Histochem. 2011;113(3):236–47.PubMed CentralView ArticlePubMedGoogle Scholar
- Rini JM. Lectin structure. Annu Rev Biophys Biomol Struct. 1995;24:551–77.View ArticlePubMedGoogle Scholar
- Sharon N, Lis H. History of lectins: from hemagglutinins to biological recognition molecules. Glycobiology. 2004;14(11):53R–62R.View ArticlePubMedGoogle Scholar
- Clemetson KJ, Morita T, Manjunatha KR. Registry of exogenous hemostatic factors of SSC of the ISTH. Scientific and standardization committee communications: classification and nomenclature of snake venom C-type lectins and related proteins. J Thromb Haemost. 2009;7(2):360.View ArticlePubMedGoogle Scholar
- Clemetson KJ. Snaclecs (snake C-type lectins) that inhibit or activate platelets by binding to receptors. Toxicon. 2010;56(7):1236–46.View ArticlePubMedGoogle Scholar
- Abreu PA, Albuquerque MG, Rodrigues CR, Castro HC. Structure-function inferences based on molecular modeling, sequence-based methods and biological data analysis of snake venom lectins. Toxicon. 2006;48(6):690–701.View ArticlePubMedGoogle Scholar
- Flexner S, Noguchi H. Snake venom in relation to haemolysis, bacteriolysis, and toxicity. J Exp Med. 1902;6:277–301.PubMed CentralView ArticlePubMedGoogle Scholar
- Gartner TK, Stocker K, Williams DC. Thrombolectin: a lectin isolated from Bothrops atrox venom. FEBS Lett. 1980;117(1):13–6.View ArticlePubMedGoogle Scholar
- Gartner TK, Ogilvie ML. Isolation and characterization of three Ca2 + −dependent beta-galactoside-specific lectins from snake venoms. Biochem J. 1984;224(1):301–7.PubMed CentralView ArticlePubMedGoogle Scholar
- Ogilvie ML, Dockter ME, Wenz L, Gartner TK. Isolation and characterization of lactose-binding lectins from the venoms of the snakes Lachesis muta and Dendroaspis jamesonii. J Biochem. 1986;100(6):1425–31.PubMedGoogle Scholar
- Lomonte B, Rojas G, Gutiérrez JM, Ramírez G. Isolation of a galactose-binding lectin from the venom of the snake Bothrops godmani (Godmann's pit viper). Toxicon. 1990;28(1):75–81.View ArticlePubMedGoogle Scholar
- Ozeki Y, Matsui T, Hamako J, Suzuki M, Fujimura Y, Yoshida E, et al. C-type galactoside-binding lectin from Bothrops jararaca venom: comparison of its structure and function with those of botrocetin. Arch Biochem Biophys. 1994;308(1):306–10.View ArticlePubMedGoogle Scholar
- Nikai T, Suzuki J, Komori Y, Ohkura M, Ohizumi Y, Sugihara H. Primary structure of the lectin from the venom of Bitis arietans (puff-adder). Biol Pharm Bull. 1995;18(11):1620–2.View ArticlePubMedGoogle Scholar
- de Carvalho DD, Marangoni S, Oliveira B, Novello JC. Isolation and characterization of a new lectin from the venom of the snake Bothrops jararacussu. IUBMB Life. 1998;44(5):933–8.View ArticleGoogle Scholar
- Komori Y, Nikai T, Tohkai T, Sugihara H. Primary structure and biological activity of snake venom lectin (APL) from Agkistrodon p. piscivorus (Eastern cottonmouth). Toxicon. 1999;37(7):1053–64.View ArticlePubMedGoogle Scholar
- Guimarães-Gomes V, Oliveira-Carvalho AL, Junqueira-de-Azevedo IL, Dutra DL S, Pujol-Luz M, Castro HC, et al. Cloning, characterization, and structural analysis of a C-type lectin from Bothrops insularis (BiL) venom. Arch Biochem Biophys. 2004;432(1):1–11.View ArticlePubMedGoogle Scholar
- Havt A, Toyama MH, do Nascimento NR, Toyama DO, Nobre AC, Martins AM, et al. A new C-type animal lectin isolated from Bothrops pirajai is responsible for the snake venom major effects in the isolated kidney. Int J Biochem Cell Biol. 2005;37(1):130–41.View ArticlePubMedGoogle Scholar
- Hamako J, Suzuki Y, Hayashi N, Kimura M, Ozeki Y, Hashimoto K, et al. Amino acid sequence and characterization of C-type lectin purified from the snake venom of Crotalus ruber. Comp Biochem Physiol B Biochem Mol Biol. 2007;146(3):299–306.View ArticlePubMedGoogle Scholar
- Mendonça-Franqueiro EP, Alves-Paiva RM, Sartim MA, Callejon DR, Paiva HH, Antonucci GA, et al. Isolation, functional, and partial biochemical characterization of galatrox, an acidic lectin from Bothrops atrox snake venom. Acta Biochim Biophys Sin. 2011;43(3):181–92.View ArticleGoogle Scholar
- Nunes ES, Souza MA, Vaz AF, Santana GM, Gomes FS, Coelho LC, et al. Purification of a lectin with antibacterial activity from Bothrops leucurus snake venom. Comp Biochem Physiol B Biochem Mol Biol. 2011;159(1):57–63.View ArticleGoogle Scholar
- Castanheira LE, Nunes DC, Cardoso TM, Santos PS, Goulart LR, Rodrigues RS, et al. Biochemical and functional characterization of a C-type lectin (BpLec) from Bothrops pauloensis snake venom. Int J Biol Macromol. 2013;54:57–64.View ArticlePubMedGoogle Scholar
- Walker JR, Nagar B, Young NM, Hirama T, Rini JM. X-ray crystal structure of a galactose-specific C-type lectin possessing a novel decameric quaternary structure. Biochemistry. 2004;43(13):3783–92.View ArticlePubMedGoogle Scholar
- Hirabayashi J, Kusunoki T, Kasai K. Complete primary structure of a galactose-specific lectin from the venom of the rattlesnake Crotalus atrox. Homologies with Ca2(+)-dependent-type lectins. J Biol Chem. 1991;266(4):2320–6.PubMedGoogle Scholar
- Barbosa PSF, Martins AMC, Toyama MH, Joazeiro PP, Beriam LOS, Fonteles MC, et al. Purification and biological effects of a C-type lectin isolated from Bothrops moojeni. J Venom Anim Toxins incl Trop Dis. 2010;16(3):493–504.View ArticleGoogle Scholar
- de Carvalho DD, Marangoni S, Novello JC. Primary structure characterization of Bothrops jararacussu snake venom lectin. J Protein Chem. 2002;21(1):43–50.View ArticlePubMedGoogle Scholar
- Aragón-Ortiz F, Mentele R, Auerswald EA. Amino acid sequence of a lectin-like protein from Lachesis muta stenophyrs venom. Toxicon. 1996;34(7):763–9.View ArticlePubMedGoogle Scholar
- Nikai T, Kato S, Komori Y, Sugihara H. Amino acid sequence and biological properties of the lectin from the venom of Trimeresurus okinavensis (Himehabu). Toxicon. 2000;38(5):707–11.View ArticlePubMedGoogle Scholar
- Xu Q, Wu XF, Xia QC, Wang KY. Cloning of a galactose-binding lectin from the venom of Trimeresurus stejnegeri. Biochem J. 1999;341(Pt 3):733–7.PubMed CentralPubMedGoogle Scholar
- Basic local alignment search tool (BLAST): http://blast.be-md.ncbi.nlm.nih.gov/.
- Aragón-Ortíz F, Brenes-Brenes JR, Gubensek F. Characterization of a lectin-like protein isolated from Lachesis muta snake venom. Rev Biol Trop. 1989;37(1):79–83.PubMedGoogle Scholar
- Drickamer K. Engineering galactose-binding activity into a C-type mannose-binding protein. Nature. 1992;360(6400):183–6.View ArticlePubMedGoogle Scholar
- Lee RT, Ichikawa Y, Fay M, Drickamer K, Shao MC, Lee YC. Ligand-binding characteristics of rat serum-type mannose-binding protein (MBP-A). Homology of binding site architecture with mammalian and chicken hepatic lectins. J Biol Chem. 1991;266(8):4810–5.PubMedGoogle Scholar
- Silva Jr FP, Alexandre GM, Ramos CH, De-Simone SG. On the quaternary structure of a C-type lectin from Bothrops jararacussu venom--BJ-32 (BjcuL). Toxicon. 2008;52(8):944–53.View ArticlePubMedGoogle Scholar
- Sartim MA, Riul TB, Del Cistia-Andrade C, Stowell SR, Arthur CM, Sorgi CA, et al. Galatrox is a C-type lectin in Bothrops atrox snake venom that selectively binds LacNAc-terminated glycans and can induce acute inflammation. Glycobiology. 2014;24(11):1010–21.View ArticlePubMedGoogle Scholar
- Gabius HJ, André S, Kaltner H, Siebert HC. The sugar code: functional lectinomics. Biochim Biophys Acta. 2002;1572(2–3):165–77.View ArticlePubMedGoogle Scholar
- Gemeiner P, Mislovicová D, Tkác J, Svitel J, Pätoprstý V, Hrabárová E, et al. Lectinomics II. A highway to biomedical/clinical diagnostics. Biotechnol Adv. 2009;27(1):1–15.View ArticlePubMedGoogle Scholar
- Earl ST, Robson J, Trabi M, de Jersey J, Masci PP, Lavin MF. Characterisation of a mannose-binding C-type lectin from Oxyuranus scutellatus snake venom. Biochimie. 2011;93(3):519–27.View ArticlePubMedGoogle Scholar
- Liang XL, Wang KY. Isolation and characterization of a lectin from the venom of snake Trimeresurus stejnegeri Schidmt. Acta Biochem Biophys Sin. 1993;25:515–21.Google Scholar
- Hirata Y, Ito M, Nikai T, Kato S, Komori Y, Sugiura H, et al. Himehabu lectin, a novel inducer of Ca2 + −release from the venom of the snake Trimeresurus okinavensis, in sarcoplasmic reticulum. J Pharm Pharmacol. 1999;51(10):1207–11.View ArticlePubMedGoogle Scholar
- De-Simone SG, Netto CC, Silva Jr FP. Simple affinity chromatographic procedure to purify beta-galactoside binding lectins. J Chromatogr B Analyt Technol Biomed Life Sci. 2006;838(2):135–8.View ArticlePubMedGoogle Scholar
- Panunto PC, da Silva MA, Linardi A, Buzin MP, Melo SE, Mello SM, et al. Biological activities of a lectin from Bothrops jararacussu snake venom. Toxicon. 2006;47(1):21–31.View ArticlePubMedGoogle Scholar
- Young NM, van Faassen H, Watson DC, Mackenzie CR. Specificity analysis of the C-type lectin from rattlesnake venom, and its selectivity towards Gal- or GalNAc-terminated glycoproteins. Glycoconj J. 2011;28(6):427–35.View ArticlePubMedGoogle Scholar
- Heimburg-Molinaro J, Song X, Smith DF, Cummings RD. Preparation and analysis of glycan microarrays. Curr Protoc Protein Sci. 2011;Chapter 12:Unit12.10.
- Varki A. Multiple changes in sialic acid biology during human evolution. Glycoconj J. 2009;26(3):231–45.View ArticlePubMedGoogle Scholar
- Sharon N, Lis H. Lectins as cell recognition molecules. Science. 1989;246(4927):227–34.View ArticlePubMedGoogle Scholar
- Mastro AM, Hurley DJ, Winning RK, Filipowski R, Ogilvie ML, Gartner TK. Mitogenic activity of snake venom lectins. Cell Tissue Kinet. 1986;19(5):557–66.PubMedGoogle Scholar
- Ohkura M, Miyashita Y, Nikai T, Suzuki J, Komori Y, Sugihara H, et al. Properties of Ca++ release induced by puff adder lectin, a novel lectin from the snake Bitis arietans, in sarcoplasmic reticulum. J Pharmacol Exp Ther. 1996;277(2):1043–8.PubMedGoogle Scholar
- Braga MD, Martins AM, Amora DN, de Menezes DB, Toyama MH, Toyama DO, et al. Purification and biological effects of C-type lectin isolated from Bothrops insularis venom. Toxicon. 2006;47(8):859–67.View ArticlePubMedGoogle Scholar
- Elifio-Esposito S, Tomazeli L, Schwartz C, Gimenez AP, Fugii GM, Fernandes LC, et al. Human neutrophil migration and activation by BJcuL, a galactose binding lectin purified from Bothrops jararacussu venom. BMC Immunol. 2011;12:10.PubMed CentralView ArticlePubMedGoogle Scholar
- Nowell PC. Phytohemagglutinin: an initiator of mitosis in cultures of normal human leukocytes. Cancer Res. 1960;20:462–6.PubMedGoogle Scholar
- Ogilvie ML, Byl JW, Gartner TK. Platelet-aggregation is stimulated by lactose-inhibitable snake venom lectins. Thromb Haemost. 1989;62(2):704–7.PubMedGoogle Scholar
- Dias-Baruffi M, Roque-Barreira MC, Cunha FQ, Ferreira SH. Biological characterization of purified macrophage-derived neutrophil chemotactic factor. Mediators Inflamm. 1995;4(4):263–9.PubMed CentralView ArticlePubMedGoogle Scholar
- Dias-Baruffi M, Roque-Barreira MC, Cunha FQ, Ferreira SH. Isolation and partial chemical characterization of macrophage-derived neutrophil chemotactic factor. Mediators Inflamm. 1995;4(4):257–62.PubMed CentralView ArticlePubMedGoogle Scholar
- Rabinovich GA, Sotomayor CE, Riera CM, Bianco I, Correa SG. Evidence of a role for galectin-1 in acute inflammation. Eur J Immunol. 2000;30(5):1331–9.View ArticlePubMedGoogle Scholar
- Stowell SR, Qian Y, Karmakar S, Koyama NS, Dias-Baruffi M, Leffler H, et al. Differential roles of galectin-1 and galectin-3 in regulating leukocyte viability and cytokine secretion. J Immunol. 2008;180(5):3091–102.View ArticlePubMedGoogle Scholar
- Santiago MQ, Leitão CC, Pereira Jr FN, Pinto Jr VR, Osterne VJ, Lossio CF, et al. Purification, characterization and partial sequence of a pro-inflammatory lectin from seeds of Canavalia oxyphylla Standl. & L. O. Williams. J Mol Recognit. 2014;27(3):117–23.View ArticlePubMedGoogle Scholar
- Gómez Leiva MA, Aragón-Ortiz F. Purification and some properties of hemagglutinating protein mutina from bushmaster Lachesis muta snake venom. Rev Biol Trop. 1986;34(1):49–53.PubMedGoogle Scholar
- Elifio-Esposito SL, Hess PL, Moreno AN, Lopes-Ferreira M, Ricart CAO, Souza MV, et al. A C-type lectin from Bothrops jararacussu venom can adhere to extracellular matrix proteins and induce the rolling of leukocytes. J Venom Anim Toxins incl Trop Dis. 2007;13(4):782–99.View ArticleGoogle Scholar
- León G, Sánchez L, Hernández A, Villalta M, Herrera M, Segura A, et al. Immune response towards snake venoms. Inflamm Allergy Drug Targets. 2011;10(5):381–98.View ArticlePubMedGoogle Scholar
- Warrell DA. Venomous bites, stings, and poisoning. Infect Dis Clin North Am. 2012;26(2):207–23.View ArticlePubMedGoogle Scholar
- Sitprija V, Sitprija S. Renal effects and injury induced by animal toxins. Toxicon. 2012;60(5):943–53.View ArticlePubMedGoogle Scholar
- Lanner JT. Ryanodine receptor physiology and its role in disease. Adv Exp Med Biol. 2012;740:217–34.View ArticlePubMedGoogle Scholar
- Mukhopadhyay S, Plüddemann A, Gordon S. Macrophage pattern recognition receptors in immunity, homeostasis and self tolerance. Adv Exp Med Biol. 2009;653:1–14.View ArticlePubMedGoogle Scholar
- Goodridge HS, Wolf AJ, Underhill DM. Beta-glucan recognition by the innate immune system. Immunol Rev. 2009;230(1):38–50.View ArticlePubMedGoogle Scholar
- Messner P, Schaffer C, Kosma P. Bacterial cell-envelope glycoconjugates. In: Horton D, editor. Advances in carbohydrate chemistry and biochemistry. 2013;69:209–72.PubMed CentralView ArticlePubMedGoogle Scholar
- Kim YJ, Varki A. Perspectives on the significance of altered glycosylation of glycoproteins in cancer. Glycoconj J. 1997;14(5):569–76.View ArticlePubMedGoogle Scholar
- Powlesland AS, Hitchen PG, Parry S, Graham SA, Barrio MM, Elola MT, et al. Targeted glycoproteomic identification of cancer cell glycosylation. Glycobiology. 2009;19(8):899–909.PubMed CentralView ArticlePubMedGoogle Scholar
- Nolte S, de Castro DD, Baréa AC, Gomes J, Magalhães A, Mello Zischler LF, et al. BJcuL, a lectin purified from Bothrops jararacussu venom, induces apoptosis in human gastric carcinoma cells accompanied by inhibition of cell adhesion and actin cytoskeleton disassembly. Toxicon. 2012;59(1):81–5.View ArticlePubMedGoogle Scholar
- Damasio DC, Nolte S, Polak LP, Brandt AP, Bonan NB, Zischler L, et al. The lectin BJcuL induces apoptosis through TRAIL expression, caspase cascade activation and mitochondrial membrane permeability in a human colon adenocarcinoma cell line. Toxicon. 2014;90:299–307.View ArticleGoogle Scholar
- Nunes ES, Souza MA, Vaz AF, Silva TG, Aguiar JS, Batista AM, et al. Cytotoxic effect and apoptosis induction by Bothrops leucurus venom lectin on tumor cell lines. Toxicon. 2012;59(7–8):667–71.View ArticlePubMedGoogle Scholar
- Debatin KM. Apoptosis pathways in cancer and cancer therapy. Cancer Immunol Immunother. 2004;53(3):153–9.View ArticlePubMedGoogle Scholar
- Aranda-Souza MA, Rossato FA, Costa RA, Figueira TR, Castilho RF, Guarniere MC, et al. A lectin from Bothrops leucurus snake venom raises cytosolic calcium levels and promotes B16-F10 melanoma necrotic cell death via mitochondrial permeability transition. Toxicon. 2014;82:97–103.View ArticlePubMedGoogle Scholar
- ESPript 3.0: http://espript.ibcp.fr/ESPript/cgi-bin/ESPript.cgi.
- de Carvalho DD, Schmitmeier S, Novello JC, Markland FS. Effect of BJcuL (a lectin from the venom of the snake Bothrops jararacussu) on adhesion and growth of tumor and endothelial cells. Toxicon. 2001;39(10):1471–6.View ArticlePubMedGoogle Scholar