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Papers by Eduardo M Cilli

Research paper thumbnail of Nanostructured functional peptide films and their application in C-reactive protein immunosensors

Zenodo (CERN European Organization for Nuclear Research), Dec 5, 2020

Research paper thumbnail of Understanding the mechanism of action of peptide (p-BthTX-I)2 derived from C-terminal region of phospholipase A2 (PLA2)-like bothropstoxin-I on Gram-positive and Gram-negative bacteria

Toxicon, Jun 1, 2021

Based on the antimicrobial activity of bothropstoxin-I (BthTX-I) and on the premise that a C-term... more Based on the antimicrobial activity of bothropstoxin-I (BthTX-I) and on the premise that a C-terminal peptide of Lys49 myotoxin can reproduce the antimicrobial activity of the parent protein, we aimed to study the mechanism of action of a peptide derived from the C-terminal region of the myotoxin BthTX-I [(p-BthTX-I)2, sequence: KKYRYHLKPFCKK, disulfide-linked dimer] against Gram-positive and Gram-negative bacteria. Fluorescence quenching technique showed that the carboxyfluorescein labeled-peptide [CF-(p-BthTX-I)2] when incubated with E. coli displayed a superior penetration activity than when incubated with S. aureus. Cell death induced by the peptide (p-BthTX-I)2 showed a loss of membrane integrity in E. coli and S. aureus; however, the mechanisms of cell death were different, characterized by the presence of necrosis-like and apoptosis-like deaths, respectively. Scanning electron microscopy studies in E. coli and S. aureus showed morphological changes in the cells, with superficial deformities, appearance of wrinkles and bubbles, and formation of vesicles. Our results demonstrate that the mechanism of action of the peptide (p-BthTX-I)2 is different in Gram-negative (E. coli) and Gram-positive (S. aureus) bacteria. Knowledge of the mechanism of action of these peptides is important, since they are promising prototypes for new antimicrobial drugs.

Research paper thumbnail of P13-034-23 Peptides From Cowpea β-Vignin Exerted Anticancer Effect by Causing Apoptosis and Cell Cycle Arrest in Colon Cancer Cells

Current developments in nutrition, Jul 1, 2023

Research paper thumbnail of Estudo químico de Jatropha curcas e de J. gossypifolia nativas e cultivadas: Avaliação de ciclopeptídeos em função de habitat e hábito: prospecção e atividade biológica

Research paper thumbnail of New Strategies for Novel Drugs: Antimicrobial Peptides Containing Ferrocene with Improved Antifungal and Antiplasmodial Biological Activity

Protein and Peptide Letters, Dec 1, 2022

Background: Fungal and parasitic diseases are global health problems, and the available treatment... more Background: Fungal and parasitic diseases are global health problems, and the available treatments are becoming ineffective, mainly due to the emergence of resistant strains of pathogens. Furthermore, the drugs currently in use exhibit high toxicity and side effects. The scarcity of efficient treatments for fungal and parasitic diseases has motivated the search for new drug candidates, including antimicrobial peptides. The chemokine class RP1 peptide shows inhibitory activity against bacteria, viruses, cancer cells and parasites. In addition, the organometallic compound ferrocene showed antiparasitic activity. Objective: Study aimed to assess the effect of conjugation of the RP1 peptide with ferrocene in terms of its structure, biological activity against fungi and parasites and toxicity. Methods: Peptides and conjugates were synthesized using solid phase peptide synthesis (SPPS). The Fc-RP1 peptide showed antifungal and antimalarial activities with low toxicity in the U87 and HepG2 cell lines. Results: The mechanism of action of these peptides, analyzed by flow cytometry in the fungus Cryptococcus neoformans, was through membrane permeabilization, with an emphasis on the Fc-RP1 peptide that presented the highest rate of PI-positive cell marking. Conclusion: In conclusion, ferrocene conjugated to antimicrobial peptide RP1 is an attractive biomolecule for drug discovery against fungal and parasitic diseases.

Research paper thumbnail of Effect of analogues of cationic peptides on dentin mineralization markers in odontoblast-like cells

Archives of Oral Biology, Jul 1, 2019

Research paper thumbnail of Cytotoxicity and the effect of cationic peptide fragments against cariogenic bacteria under planktonic and biofilm conditions

Research paper thumbnail of Novel Selective and Low-Toxic Inhibitor of LmCPB2.8ΔCTE (CPB) One Important Cysteine Protease for Leishmania Virulence

Biomolecules, Dec 19, 2022

Research paper thumbnail of Efficacy of the combination of P5 peptide and photodynamic therapy mediated by bixin and chlorin-e6 against Cutibacterium acnes biofilm

Photodiagnosis and Photodynamic Therapy

Research paper thumbnail of Cytocompatibility and Synergy of EGCG and Cationic Peptides Against Bacteria Related to Endodontic Infections, in Planktonic and Biofilm Conditions

Probiotics and Antimicrobial Proteins, 2021

Research paper thumbnail of Cytotoxicity and antimicrobial activity of synthetic peptides alone or in combination with conventional antimicrobials against fish pathogenic bacteria

Journal of Applied Microbiology, 2021

This study aimed to evaluate the in vitro cytotoxicity and efficacy of synthetic host defence pep... more This study aimed to evaluate the in vitro cytotoxicity and efficacy of synthetic host defence peptides (HDPs), alone or in combination with florfenicol (FFC), oxytetracycline (OTC) or thiamphenicol (TAP), against different pathogenic bacteria isolated from diseased fish.

Research paper thumbnail of Evaluation of peptides release using a natural rubber latex biomembrane as a carrier

Research paper thumbnail of New molecular features of cowpea bean (Vigna unguiculata, l. Walp) β-vignin

Bioscience, biotechnology, and biochemistry, 2018

Cowpea seed β-vignin, a vicilin-like globulin, proved to exert various health favourable effects,... more Cowpea seed β-vignin, a vicilin-like globulin, proved to exert various health favourable effects, including blood cholesterol reduction in animal models. The need of a simple scalable enrichment procedure for further studies for tailored applications of this seed protein is crucial. A chromatography-independent fractionation method allowing to obtain a protein preparation with a high degree of homogeneity was used. Further purification was pursued to deep the molecular characterisation of β-vignin. The results showed: (i) differing glycosylation patterns of the two constituent polypeptides, in agreement with amino acid sequence features; (ii) the seed accumulation of a gene product never identified before; (iii) metal binding capacity of native protein, a property observed only in few other legume seed vicilins.

Research paper thumbnail of Antimicrobial peptide-loaded liquid crystalline precursor bioadhesive system for the prevention of dental caries

International journal of nanomedicine, 2018

Anticaries agents must interfere with the adhesion of and its proliferation in dental biofilm, wi... more Anticaries agents must interfere with the adhesion of and its proliferation in dental biofilm, without causing host toxicity and bacterial resistance. Natural substances, including cationic antimicrobial peptides (CAMPs) and their fragments, such as β-defensin-3 peptide fragment (D1-23), have been widely studied. However, the chemical and physical stability of CAMPs may be compromised by external factors, such as temperature and pH, reducing the period of antimicrobial activity. To overcome the aforementioned disadvantage, this study developed and character-ized a drug delivery system and evaluated the cytotoxicity and effect against biofilm of a D1-23-loaded bioadhesive liquid crystalline system (LCS). LCS was composed of oleic acid, polyoxypropylene-(5)-polyoxyethylene-(20)-cetyl alcohol, Carbopol 974P and Carbopol 971P. LCS was analyzed by polarized light microscopy (PLM), rheology (viscoelasticity and flow properties) and in vitro bioadhesion. The viability of epithelial cells w...

Research paper thumbnail of In vitro and in silico studies of 3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitory activity of the cowpea Gln-Asp-Phe peptide

Food chemistry, 2018

Previous studies have shown that cowpea protein positively interferes with cholesterol metabolism... more Previous studies have shown that cowpea protein positively interferes with cholesterol metabolism. In this study, we evaluated the ability of the fraction containing peptides of <3 kDa, as well as that of the Gln-Asp-Phe (QDF) peptide, derived from cowpea β-vignin protein, to inhibit HMG-CoA reductase activity. We established isolation and chromatography procedures to effectively obtain the protein with a purity above 95%. In silico predictions were performed to identify peptide sequences capable of interacting with HMG-CoA reductase. In vitro experiments showed that the fraction containing peptides of <3 kDa displayed inhibition of HMG-CoA reductase activity. The tripeptide QDF inhibits HMG-CoA reductase (IC = 12.8 μM) in a dose-dependent manner. Furthermore, in silico studies revealed the binding profile of the QDF peptide and hinted at the molecular interactions that are responsible for its activity. Therefore, this study shows, for the first time, a peptide from cowpea β-v...

Research paper thumbnail of KR-12-a5 is a non-cytotoxic agent with potent antimicrobial effects against oral pathogens

Biofouling, Jan 12, 2017

This study evaluated the cytotoxicity and antimicrobial activity of analogs of cationic peptides ... more This study evaluated the cytotoxicity and antimicrobial activity of analogs of cationic peptides against microorganisms associated with endodontic infections. L-929 fibroblasts were exposed to LL-37, KR-12-a5 and hBD-3-1CV and chlorhexidine (CHX, control), and cell metabolism was evaluated with MTT. The minimal inhibitory concentration (MIC) and the minimal bactericidal/fungicidal concentration (MBC/MFC) of the peptides and CHX were determined against oral pathogens associated with endodontic infections. Enterococcus faecalis and Streptococcus mutans biofilms were cultivated in bovine dentin blocks, exposed to different concentrations of the most efficient antimicrobial peptide and analyzed by confocal laser scanning microscopy. CHX and peptides affected the metabolism of L-929 at concentrations > 31.25 and 500 μg ml-1, respectively. Among the peptides, KR-12-a5 inhibited growth of both the microorganisms tested with the lowest MIC/MBC/MFC values. In addition, KR-12-a5 significan...

Research paper thumbnail of Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications

Journal of Biomaterials Science, Polymer Edition, 2017

Research paper thumbnail of Natural rubber latex: Development and in vitro characterization of a future transdermal patch for enuresis treatment

International Journal of Polymeric Materials and Polymeric Biomaterials, 2017

Research paper thumbnail of Oxytocin Sustained Release Using Natural Rubber Latex Membranes

International Journal of Peptide Research and Therapeutics, 2016

Research paper thumbnail of Author Correction: A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity

Research paper thumbnail of Nanostructured functional peptide films and their application in C-reactive protein immunosensors

Zenodo (CERN European Organization for Nuclear Research), Dec 5, 2020

Research paper thumbnail of Understanding the mechanism of action of peptide (p-BthTX-I)2 derived from C-terminal region of phospholipase A2 (PLA2)-like bothropstoxin-I on Gram-positive and Gram-negative bacteria

Toxicon, Jun 1, 2021

Based on the antimicrobial activity of bothropstoxin-I (BthTX-I) and on the premise that a C-term... more Based on the antimicrobial activity of bothropstoxin-I (BthTX-I) and on the premise that a C-terminal peptide of Lys49 myotoxin can reproduce the antimicrobial activity of the parent protein, we aimed to study the mechanism of action of a peptide derived from the C-terminal region of the myotoxin BthTX-I [(p-BthTX-I)2, sequence: KKYRYHLKPFCKK, disulfide-linked dimer] against Gram-positive and Gram-negative bacteria. Fluorescence quenching technique showed that the carboxyfluorescein labeled-peptide [CF-(p-BthTX-I)2] when incubated with E. coli displayed a superior penetration activity than when incubated with S. aureus. Cell death induced by the peptide (p-BthTX-I)2 showed a loss of membrane integrity in E. coli and S. aureus; however, the mechanisms of cell death were different, characterized by the presence of necrosis-like and apoptosis-like deaths, respectively. Scanning electron microscopy studies in E. coli and S. aureus showed morphological changes in the cells, with superficial deformities, appearance of wrinkles and bubbles, and formation of vesicles. Our results demonstrate that the mechanism of action of the peptide (p-BthTX-I)2 is different in Gram-negative (E. coli) and Gram-positive (S. aureus) bacteria. Knowledge of the mechanism of action of these peptides is important, since they are promising prototypes for new antimicrobial drugs.

Research paper thumbnail of P13-034-23 Peptides From Cowpea β-Vignin Exerted Anticancer Effect by Causing Apoptosis and Cell Cycle Arrest in Colon Cancer Cells

Current developments in nutrition, Jul 1, 2023

Research paper thumbnail of Estudo químico de Jatropha curcas e de J. gossypifolia nativas e cultivadas: Avaliação de ciclopeptídeos em função de habitat e hábito: prospecção e atividade biológica

Research paper thumbnail of New Strategies for Novel Drugs: Antimicrobial Peptides Containing Ferrocene with Improved Antifungal and Antiplasmodial Biological Activity

Protein and Peptide Letters, Dec 1, 2022

Background: Fungal and parasitic diseases are global health problems, and the available treatment... more Background: Fungal and parasitic diseases are global health problems, and the available treatments are becoming ineffective, mainly due to the emergence of resistant strains of pathogens. Furthermore, the drugs currently in use exhibit high toxicity and side effects. The scarcity of efficient treatments for fungal and parasitic diseases has motivated the search for new drug candidates, including antimicrobial peptides. The chemokine class RP1 peptide shows inhibitory activity against bacteria, viruses, cancer cells and parasites. In addition, the organometallic compound ferrocene showed antiparasitic activity. Objective: Study aimed to assess the effect of conjugation of the RP1 peptide with ferrocene in terms of its structure, biological activity against fungi and parasites and toxicity. Methods: Peptides and conjugates were synthesized using solid phase peptide synthesis (SPPS). The Fc-RP1 peptide showed antifungal and antimalarial activities with low toxicity in the U87 and HepG2 cell lines. Results: The mechanism of action of these peptides, analyzed by flow cytometry in the fungus Cryptococcus neoformans, was through membrane permeabilization, with an emphasis on the Fc-RP1 peptide that presented the highest rate of PI-positive cell marking. Conclusion: In conclusion, ferrocene conjugated to antimicrobial peptide RP1 is an attractive biomolecule for drug discovery against fungal and parasitic diseases.

Research paper thumbnail of Effect of analogues of cationic peptides on dentin mineralization markers in odontoblast-like cells

Archives of Oral Biology, Jul 1, 2019

Research paper thumbnail of Cytotoxicity and the effect of cationic peptide fragments against cariogenic bacteria under planktonic and biofilm conditions

Research paper thumbnail of Novel Selective and Low-Toxic Inhibitor of LmCPB2.8ΔCTE (CPB) One Important Cysteine Protease for Leishmania Virulence

Biomolecules, Dec 19, 2022

Research paper thumbnail of Efficacy of the combination of P5 peptide and photodynamic therapy mediated by bixin and chlorin-e6 against Cutibacterium acnes biofilm

Photodiagnosis and Photodynamic Therapy

Research paper thumbnail of Cytocompatibility and Synergy of EGCG and Cationic Peptides Against Bacteria Related to Endodontic Infections, in Planktonic and Biofilm Conditions

Probiotics and Antimicrobial Proteins, 2021

Research paper thumbnail of Cytotoxicity and antimicrobial activity of synthetic peptides alone or in combination with conventional antimicrobials against fish pathogenic bacteria

Journal of Applied Microbiology, 2021

This study aimed to evaluate the in vitro cytotoxicity and efficacy of synthetic host defence pep... more This study aimed to evaluate the in vitro cytotoxicity and efficacy of synthetic host defence peptides (HDPs), alone or in combination with florfenicol (FFC), oxytetracycline (OTC) or thiamphenicol (TAP), against different pathogenic bacteria isolated from diseased fish.

Research paper thumbnail of Evaluation of peptides release using a natural rubber latex biomembrane as a carrier

Research paper thumbnail of New molecular features of cowpea bean (Vigna unguiculata, l. Walp) β-vignin

Bioscience, biotechnology, and biochemistry, 2018

Cowpea seed β-vignin, a vicilin-like globulin, proved to exert various health favourable effects,... more Cowpea seed β-vignin, a vicilin-like globulin, proved to exert various health favourable effects, including blood cholesterol reduction in animal models. The need of a simple scalable enrichment procedure for further studies for tailored applications of this seed protein is crucial. A chromatography-independent fractionation method allowing to obtain a protein preparation with a high degree of homogeneity was used. Further purification was pursued to deep the molecular characterisation of β-vignin. The results showed: (i) differing glycosylation patterns of the two constituent polypeptides, in agreement with amino acid sequence features; (ii) the seed accumulation of a gene product never identified before; (iii) metal binding capacity of native protein, a property observed only in few other legume seed vicilins.

Research paper thumbnail of Antimicrobial peptide-loaded liquid crystalline precursor bioadhesive system for the prevention of dental caries

International journal of nanomedicine, 2018

Anticaries agents must interfere with the adhesion of and its proliferation in dental biofilm, wi... more Anticaries agents must interfere with the adhesion of and its proliferation in dental biofilm, without causing host toxicity and bacterial resistance. Natural substances, including cationic antimicrobial peptides (CAMPs) and their fragments, such as β-defensin-3 peptide fragment (D1-23), have been widely studied. However, the chemical and physical stability of CAMPs may be compromised by external factors, such as temperature and pH, reducing the period of antimicrobial activity. To overcome the aforementioned disadvantage, this study developed and character-ized a drug delivery system and evaluated the cytotoxicity and effect against biofilm of a D1-23-loaded bioadhesive liquid crystalline system (LCS). LCS was composed of oleic acid, polyoxypropylene-(5)-polyoxyethylene-(20)-cetyl alcohol, Carbopol 974P and Carbopol 971P. LCS was analyzed by polarized light microscopy (PLM), rheology (viscoelasticity and flow properties) and in vitro bioadhesion. The viability of epithelial cells w...

Research paper thumbnail of In vitro and in silico studies of 3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitory activity of the cowpea Gln-Asp-Phe peptide

Food chemistry, 2018

Previous studies have shown that cowpea protein positively interferes with cholesterol metabolism... more Previous studies have shown that cowpea protein positively interferes with cholesterol metabolism. In this study, we evaluated the ability of the fraction containing peptides of <3 kDa, as well as that of the Gln-Asp-Phe (QDF) peptide, derived from cowpea β-vignin protein, to inhibit HMG-CoA reductase activity. We established isolation and chromatography procedures to effectively obtain the protein with a purity above 95%. In silico predictions were performed to identify peptide sequences capable of interacting with HMG-CoA reductase. In vitro experiments showed that the fraction containing peptides of <3 kDa displayed inhibition of HMG-CoA reductase activity. The tripeptide QDF inhibits HMG-CoA reductase (IC = 12.8 μM) in a dose-dependent manner. Furthermore, in silico studies revealed the binding profile of the QDF peptide and hinted at the molecular interactions that are responsible for its activity. Therefore, this study shows, for the first time, a peptide from cowpea β-v...

Research paper thumbnail of KR-12-a5 is a non-cytotoxic agent with potent antimicrobial effects against oral pathogens

Biofouling, Jan 12, 2017

This study evaluated the cytotoxicity and antimicrobial activity of analogs of cationic peptides ... more This study evaluated the cytotoxicity and antimicrobial activity of analogs of cationic peptides against microorganisms associated with endodontic infections. L-929 fibroblasts were exposed to LL-37, KR-12-a5 and hBD-3-1CV and chlorhexidine (CHX, control), and cell metabolism was evaluated with MTT. The minimal inhibitory concentration (MIC) and the minimal bactericidal/fungicidal concentration (MBC/MFC) of the peptides and CHX were determined against oral pathogens associated with endodontic infections. Enterococcus faecalis and Streptococcus mutans biofilms were cultivated in bovine dentin blocks, exposed to different concentrations of the most efficient antimicrobial peptide and analyzed by confocal laser scanning microscopy. CHX and peptides affected the metabolism of L-929 at concentrations > 31.25 and 500 μg ml-1, respectively. Among the peptides, KR-12-a5 inhibited growth of both the microorganisms tested with the lowest MIC/MBC/MFC values. In addition, KR-12-a5 significan...

Research paper thumbnail of Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications

Journal of Biomaterials Science, Polymer Edition, 2017

Research paper thumbnail of Natural rubber latex: Development and in vitro characterization of a future transdermal patch for enuresis treatment

International Journal of Polymeric Materials and Polymeric Biomaterials, 2017

Research paper thumbnail of Oxytocin Sustained Release Using Natural Rubber Latex Membranes

International Journal of Peptide Research and Therapeutics, 2016

Research paper thumbnail of Author Correction: A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity