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Dive into the research topics where Tatiane Santi-Gadelha is active.

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Featured researches published by Tatiane Santi-Gadelha.


BMC Structural Biology | 2007

Structure of a lectin from Canavalia gladiata seeds: new structural insights for old molecules

Plínio Delatorre; Bruno Anderson Matias Rocha; Emmanuel P. Souza; Taianá Maia de Oliveira; Gustavo Arruda Bezerra; Frederico B. M. B. Moreno; Beatriz T. Freitas; Tatiane Santi-Gadelha; Alexandre Holanda Sampaio; Walter Filgueira de Azevedo; Benildo Sousa Cavada

BackgroundLectins are mainly described as simple carbohydrate-binding proteins. Previous studies have tried to identify other binding sites, which possible recognize plant hormones, secondary metabolites, and isolated amino acid residues. We report the crystal structure of a lectin isolated from Canavalia gladiata seeds (CGL), describing a new binding pocket, which may be related to pathogen resistance activity in ConA-like lectins; a site where a non-protein amino-acid, α-aminobutyric acid (Abu), is bound.ResultsThe overall structure of native CGL and complexed with α-methyl-mannoside and Abu have been refined at 2.3 Å and 2.31 Å resolution, respectively. Analysis of the electron density maps of the CGL structure shows clearly the presence of Abu, which was confirmed by mass spectrometry.ConclusionThe presence of Abu in a plant lectin structure strongly indicates the ability of lectins on carrying secondary metabolites. Comparison of the amino acids composing the site with other legume lectins revealed that this site is conserved, providing an evidence of the biological relevance of this site. This new action of lectins strengthens their role in defense mechanisms in plants.


Molecules | 2012

Antinociceptive and Anti-inflammatory Effects of a Lectin-Like Substance from Clitoria fairchildiana R. Howard Seeds

Joana Filomena Magalhães Leite; Ana Maria Sampaio Assreuy; Mário Rogério Lima Mota; Pedro Henrique de Souza Ferreira Bringel; Rodrigo Rodrigues e Lacerda; Vinicius de Morais Gomes; João Batista Cajazeiras; Kyria S. Nascimento; Hilzeth de Luna Freire Pessôa; Carlos Alberto de Almeida Gadelha; Plínio Delatorre; Benildo Sousa Cavada; Tatiane Santi-Gadelha

Lectins are proteins that have the ability to bind specifically and reversibly to carbohydrates and glycoconjugates, without altering the structure of the glycosyl ligand. They are found in organisms such as viruses, plants and humans, and they have been shown to possess important biological activities. The objective of this study was to purify and characterize lectins in the seeds of Clitoria fairchildiana, as well as to verify their biological activities. The results indicated the presence of a lectin (CFAL) in the glutelin acid protein fraction, which agglutinated native rabbit erythrocytes. CFAL was purified by column chromatography ion-exchange, DEAE-Sephacel, which was obtained from a peak of protein retained in the matrix by applying 0.5 M NaCl using the step-wise method. Electrophoretic analysis of this lectin in SDS-PAGE indicated a two band pattern protein molecular mass of approximately 100 and 116 kDa. CFAL proved to be unspecific to all carbohydrates/glycoconjugates in common use for the sugar inhibition test. This lectin showed no significant cytotoxicity to human red blood cells. It was observed that CFAL has anti-inflammatory activity in the paw edema induced by carrageenan model, in which a 64% diminution in edema was observed. Antinociceptive effects were observed for CFAL in the abdominal writhing test (induced by acetic acid), in which increasing doses of the lectin caused reduction in the number of contortions by up to 72%. It was concluded that the purified and characterized lectin from the seeds of Clitoria fairchildiana has anti-inflammatory and antinociceptive activity, and is not cytotoxic to human erythrocytes.


PLOS ONE | 2014

Comparative Protein Composition Analysis of Goat Milk Produced by the Alpine and Saanen Breeds in Northeastern Brazil and Related Antibacterial Activities

Whyara Karoline Almeida da Costa; Evandro Leite de Souza; Edvaldo Mesquita Beltrão-Filho; Gracy Kelly Vieira Vasconcelos; Tatiane Santi-Gadelha; Carlos Alberto de Almeida Gadelha; Octavio L. Franco; Rita de Cássia Ramos do Egypto Queiroga; Marciane Magnani

The protein composition of goat milk differs between goat breeds and could present regional trends. The aim of this study was to comparatively analyze the protein composition of goat milk produced by the Alpine and Saanen breeds in northeastern Brazil and to evaluate the antibacterial activity of its protein fractions. SDS-PAGE, 2-DE electrophoresis and RP-HPLC analyses revealed the absence of αs1-casein in the milk of both breeds and no differences between the αs2-casein, β-casein, β-lactoglobulin and α-lactalbumin profiles. The amounts of soluble proteins and β-casein hydrolysis residues were higher in Saanen milk. Only the protein fraction containing the largest amounts of casein (F60–90%) inhibited bacterial growth, with MIC values between 50 and 100 mg/mL. This study describe for the first time three important points about the goat milk protein of two Brazilian goat breeders: absence of α-s1 casein in the protein profile, differences between the milk protein composition produced by goats of Alpine and Saanen breeders and antibacterial activity of unbroken proteins (casein-rich fraction) present in these milk.


Biochimie | 2012

Structure of Dioclea virgata lectin: Relations between carbohydrate binding site and nitric oxide production

Raphael Batista da Nóbrega; Bruno Anderson Matias Rocha; Carlos Alberto de Almeida Gadelha; Tatiane Santi-Gadelha; Alana de Freitas Pires; Ana Maria Sampaio Assreuy; Kyria S. Nascimento; Celso Shiniti Nagano; Alexandre Holanda Sampaio; Benildo Sousa Cavada; Plínio Delatorre

The lectin of Dioclea virgata (DvirL), both native and complexed with X-man, was submitted to X-ray diffraction analysis and the crystal structure was compared to that of other Diocleinae lectins in order to better understand differences in biological properties, especially with regard to the ability of lectins to induce nitric oxide (NO) production. An association was observed between the volume of the carbohydrate recognition domain (CRD), the ability to induce NO production and the relative positions of Tyr12, Arg228 and Leu99. Thus, differences in biological activity induced by Diocleinae lectins are related to the configuration of amino acid residues in the carbohydrate binding site and to the structural conformation of subsequent regions capable of influencing site-ligand interactions. In conclusion, the ability of Diocleinae lectins to induce NO production depends on CRD configuration.


Epilepsy & Behavior | 2009

Central action of Araucaria angustifolia seed lectin in mice

Silvânia Maria Mendes Vasconcelos; Silvane R. Lima; Paula Matias Soares; Ana Maria Sampaio Assreuy; Francisca Cléa Florenço de Sousa; Rodrigo de Freitas Guimarães Lobato; Germana Silva Vasconcelos; Tatiane Santi-Gadelha; Eduardo Henrique Salviano Bezerra; Benildo Sousa Cavada; Manoel Cláudio Azevedo Patrocínio

Possible central nervous system effects of the gymnosperm lectin from Araucaria angustifolia seeds were studied in seizure and open field tests. Male Swiss mice were administered saline (control), lectin (0.1, 1, and 10 mg/kg), flumazenil (1 mg/kg), or diazepam (1 mg/kg) intraperitoneally. Lectin at the highest dose increased time to death in the pentylenetetrazole- and strychnine-induced seizure models as compared with control, but not in the pilocarpine model. In the open field test, lectin reduced locomotor activity at all doses tested, as did diazepam, when compared with control. These locomotor effects were reversed by flumazenil pretreatment. In conclusion, A. angustifolia lectin had a protective effect in the pentylenetetrazole- and strychnine-induced seizure models, suggestive of activity in the GABAergic and glycinergic systems, respectively, and also caused a reduction in animal movements, which was reversed by flumazenil, pointing to a depressant action mediated by a GABAergic mechanism.


Biochimie | 2013

Interactions between indole-3-acetic acid (IAA) with a lectin from Canavalia maritima seeds reveal a new function for lectins in plant physiology

Plínio Delatorre; Jose Caetano Silva-Filho; Bruno Anderson Matias Rocha; Tatiane Santi-Gadelha; Raphael Batista da Nóbrega; Carlos Alberto de Almeida Gadelha; Kyria S. Nascimento; Celso Shiniti Nagano; Alexandre Holanda Sampaio; Benildo Sousa Cavada

Indole-3-acetic acid (IAA) bound is considered a storage molecule and is inactive. However, some studies have proposed an additional possible regulatory mechanism based on the ability of lectins to form complexes with IAA. We report the first crystal structure of ConM in complex with IAA at 2.15 Å resolution. Based on a tetrameric model of the complex, we hypothesize how the lectin controls the availability of IAA during the early seedling stages, indicating a possible new physiological role for these proteins. A free indole group is also bound to the protein. The ConM interaction with different forms of IAA is a strategy to render the phytohormone unavailable to the cell. Thus, this new physiological role proposed for legume lectins might be a novel mechanism by which IAA levels are decreased in addition to the destruction and formation of new complexes in the later stages of seed germination.


International Immunopharmacology | 2016

Lectin from Abelmoschus esculentus reduces zymosan-induced temporomandibular joint inflammatory hypernociception in rats via heme oxygenase-1 pathway integrity and tnf-α and il-1β suppression.

Raul Sousa Freitas; Danielle Rocha do Val; Maria Ester Frota Fernandes; Francisco Isaac Fernandes Gomes; José Thalles Jocelino Gomes de Lacerda; Tatiane Santi-Gadelha; Carlos Alberto de Almeida Gadelha; Vicente de Paulo Teixeira Pinto; Gerardo Cristino-Filho; Karuza Maria Alves Pereira; Gerly Anne de Castro Brito; Mirna Marques Bezerra; Hellíada Vasconcelos Chaves

Temporomandibular joint (TMJ) disorders show inflammatory components, heavily impacting on quality of life. Abelmoschus esculentus is largely cultivated in Northeastern Brazil for medicinal purposes, having it shown anti-inflammatory activity. We evaluated A. esculentus lectin (AEL) efficacy in reducing zymosan-induced temporomandibular joint inflammatory hypernociception in rats along with the mechanism of action through which it exerts anti-inflammatory activity. Animals were pre-treated with AEL (0.01, 0.1 or 1mg/kg) before zymosan (Zy) injection in the TMJ to determine anti-inflammatory activity. To analyse the possible effect of the hemeoxygenase-1 (HO-1) and the nitric oxide (NO) pathways on AEL efficacy, animals were pre-treated with ZnPP-IX (3mg/kg), a specific HO-1 inhibitor, or aminoguanidine (30mg/kg), a selective iNOS inhibitor, before AEL administration. Von Frey test evaluated inflammatory hypernociception, synovial fluid collection was performed to determine leukocyte counting and myeloperoxidase (MPO) activity 6h after Zy injection, and Evans Blue extravasation determined vascular permeability. TMJ tissue was collected for histopathological analysis (H&E) and immunohistochemistry (TNF-α, IL-1β, HO-1). In addition, TMJ tissue and trigeminal ganglion collection was performed for TNF-α and IL-1β dosage (ELISA). AEL increased inflammatory nociceptive threshold, reduced leukocyte influx along with MPO activity, leukocyte influx into the synovial membrane, and Evans Blue extravasation. It promoted HO-1 overexpression whilst decreased TNF-α and IL-1β expression in the TMJ tissue. AEL reduced TNF-α and IL-1β levels in TMJ tissue and trigeminal ganglion. AEL effects, however, were not observed in the presence of ZnPP-IX. These findings suggest that AEL efficacy depends on TNF-α/IL-1β inhibition and HO-1 pathway integrity.


Current Pharmaceutical Design | 2016

Αlpha-2 Adrenergic and Opioids Receptors Participation in Mice Gastroprotection of Abelmoschus esculentus Lectin

Kátia Alves Ribeiro; Hellíada Vasconcelos Chaves; Samuel Mateus Pereira Filho; Isabela Ribeiro Pinto; Dina Andressa Martins Monteiro; Samuel Oliveira Matos; Tatiane Santi-Gadelha; Carlos Alberto de Almeida Gadelha; José Thalles Jocelino Gomes de Lacerda; Lissiana Magna Vasconcelos Aguiar; Karuza Maria Alves Pereira; Norma Maria Barros Benevides; Vicente de Paulo Teixeira Pinto; Gerardo Cristino Filho; Mirna Marques Bezerra; Antonio Alfredo Rodrigues e Silva

Lectins are a heterogeneous group of proteins and glycoproteins with potential role as therapeutic and diagnostic tools to combat various diseases, besides some functions on human organism. Abelmoschus esculentus (Okra), a horticultural plant of African origin, is cultivated in northeastern Brazil, and used for different medicinal purposes. This work is aimed to elucidate the action mechanisms of Abelmoschus esculentus lectin (AEL) gastro protective effect on gastropathy induced by ethanol. Fasted mice treated with Ethanol 99.9% (0.2 ml/animal, p.o.) received previously AEL (0.01, 0.1, 1.0, 10 or 50 mg/kg, i.v.), saline (5 ml/kg; i.v.) or ranitidine (80 mg/kg, p.o.) in four experimental series, in which pharmacological tools (yohimbine, naloxone, L-NAME or indomethacin), were administered with the purpose of make clear possible molecular action mechanisms. Mice were euthanized 30 min after ethanol challenge to verify the stomach damages. Establishment of gastric oxidative stress, tissue hemoglobin (Hb) content and microscopic features (H&E) were taken in order to characterize the AEL gastro protective effect. AEL (1 mg/kg) was capable of protect mucosa against ethanol damages in presence of two (L-NAME and indomethacin) of four antagonists/inhibitors used. The AEL effect was reversed by naloxone and yohimbine, showing the involvement of opioids and Αlpha-2 adrenergic receptors on gastric protective effect of this lectin. Evaluation of microscopic features, oxidative stress, and Hb levels pointed the protective effects of AEL. This activity seems to be mediated by alpha-2 adrenergic and opioid receptors activation. Nitric oxide or prostaglandins were not involved. AEL simultaneously showed antioxidant effect that is probably implicated in its intricate defensive mechanism of action.


Molecular Reproduction and Development | 2012

Involvement of ABCB1 and ABCC1 transporters in sea urchin Echinometra lucunter fertilization.

Helena Lima Silva‐Neta; Elis Torrezan; Jocelmo Cássio de Araújo Leite; Tatiane Santi-Gadelha; Luis Fernando Marques-Santos

Fertilization is an ordered sequence of cellular interactions that promotes gamete fusion to form a new individual. Since the pioneering work of Oskar Hertwig conducted on sea urchins, echinoderms have contributed to the understanding of cellular and molecular aspects of the fertilization processes. Studies on sea urchin spermatozoa reported the involvement of a plasma membrane protein that belongs to the ABC proteins superfamily in the acrosome reaction. ABC transporters are expressed in membranes of eukaryotic and prokaryotic cells, and are associated with the transport of several compounds or ions across biomembranes. We aimed to investigate ABCB1 and ABCC1 transporter activity in sea urchin spermatozoa and their involvement in fertilization. Our results indicate that Echinometra lucunter spermatozoa exhibit a low intracellular calcein accumulation (18.5% stained cells); however, the ABC blockers reversin205, verapamil, and MK571 increased dye accumulation (93.0–96.6% stained cells). We also demonstrated that pharmacologically blocking ABCB1 and ABCC1 decreased spermatozoa fertilizing capacity (70% inhibition), and this phenotype was independent of extracellular calcium. These data suggest that functional spermatozoa ABCB1 and ABCC1 transporters are crucial for a successful fertilization. Additional studies must be performed to investigate the involvement of membrane lipid homeostasis in the fertilization process. Mol. Reprod. Dev. 79: 861–869, 2012.


Acta Crystallographica Section F-structural Biology and Crystallization Communications | 2005

Crystallization and preliminary X-ray diffraction analysis of a lectin from Canavalia maritima seeds

Carlos Alberto de Almeida Gadelha; Frederico Bruno Mendes Batista Moreno; Tatiane Santi-Gadelha; João Batista Cajazeiras; Bruno Anderson Matias Rocha; Joane Kathelen Rodrigues Rustiguel; Beatriz Tupinamba Freitas; Fernanda Canduri; Plínio Delatorre; Walter Filgueira de Azevedo; Benildo Sousa Cavada

A lectin from Canavalia maritima seeds (ConM) was purified and submitted to crystallization experiments. The best crystals were obtained using the vapour-diffusion method at a constant temperature of 293 K and grew in 7 d. A complete structural data set was collected to 2.1 A resolution using a synchrotron-radiation source. The ConM crystal belongs to the orthorhombic space group P2(1)2(1)2, with unit-cell parameters a = 67.15, b = 70.90, c = 97.37 A. A molecular-replacement search found a solution with a correlation coefficient of 69.2% and an R factor of 42.5%. Crystallographic refinement is under way.

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Benildo Sousa Cavada

Federal University of Ceará

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Celso Shiniti Nagano

Federal University of Ceará

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Kyria S. Nascimento

Federal University of Ceará

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