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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Synthesis and Characterization of Peptide-Chitosan Conjugates (PepChis) with Lipid Bilayer Affinity and Antibacterial Activity

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Author(s):
Costa Petrin, Thais H. [1] ; Fadel, Valmir [2] ; Martins, Danubia B. [2] ; Dias, Susana A. [3] ; Cruz, Ana [3] ; Sergio, Luciana Marciano [4] ; Arcisio-Miranda, Manoel [4] ; Castanho, Miguel A. R. B. [3] ; dos Santos Cabrera, Marcia P. [2, 1]
Total Authors: 9
Affiliation:
[1] Univ Estadual Paulista Unesp, Inst Biociencias Letras & Ciencias Exatas Ibilce, Dept Quim & Ciencias Ambientais, Campus Sao Jose Do Rio Preto, BR-15054000 Sao Jose Do Rio Preto, SP - Brazil
[2] Univ Estadual Paulista Unesp, Inst Biociencias Letras & Ciencias Exatas Ibilce, Dept Fis, Campus Sao Jose Do Rio Preto, BR-15054000 Sao Jose Do Rio Preto, SP - Brazil
[3] Univ Lisbon, Fac Med, Inst Med Mol, P-1649028 Lisbon - Portugal
[4] Univ Fed Sao Paulo, Dept Biofis, Lab Neurobiol Estrutural & Func LaNEF, BR-04023062 Sao Paulo - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Biomacromolecules; v. 20, n. 7, p. 2743-2753, JUL 2019.
Web of Science Citations: 0
Abstract

Antimicrobial peptides appear among innovative biopolymers with potential therapeutic interest. Nevertheless, issues concerning efficiency, production costs, and toxicity persist. Herein, we show that conjugation of peptides with chitosans can represent an alternative in the search for these needs. To increase solubility, deacetylated and degraded chitosans were prepared. Then, they were functionalized via N-succinimidyl-S-acetylthiopropionate or via glutathione (GSH), an endogenous peptide linker. To the best of our knowledge, it is the first time that GSH is used as a thiolating agent for the conjugation of peptides. Next, thiolated chitosans were conjugated through a disulfide bond with designed short chain peptides, one of them derived from the antimicrobial peptide Jelleine-I. Conjugates and respective reaction intermediates were characterized by absorciometry, attenuated total reflectance-Fourier transform infrared, and H-1 NMR Zeta potential measurements showed the cationic nature of these biomacromolecules and their preferential partitioning to Gram-positive bacterial-like model membranes. In vitro investigation using representative Gram-positive and-negative bacteria (Staphylococcus aureus and Escherichia coli, respectively) showed that the conjugation strategies lead to enhanced activity in relation to the unconjugated peptide and to the unconjugated chitosan. The obtained products showed selectivity toward S. aureus at low cytotoxicity as determined in NIH/3T3 cells. Overall, our study demonstrates that an appropriate choice of antimicrobial peptide and chitosan characteristics leads to increased antimicrobial activity of the conjugated product and represents a strategy to modulate the activity and selectivity of antimicrobials resorting to low-cost chemicals. The present proposal starts from less expensive raw materials (chitosan and short-chain peptide), is based on aqueous solvents, and minimizes the use of reactants with a higher environmental impact. The final biopolymer contains the backbone of chitosan, just 3-6% peptide derived from royal jelly and GSH, all of them considered safe for human use or as a physiological molecule. (AU)

FAPESP's process: 14/08372-7 - Peptide and chitosan conjugates with pharmacological potential: synthesis, prospecting of activity in membrane mimetic systems, and evaluation in cells
Grantee:Marcia Perez dos Santos Cabrera
Support Opportunities: Scholarships in Brazil - Young Researchers
FAPESP's process: 16/13368-4 - Nanostructured systems: from membrane biomimetic models to carriers of bioactives
Grantee:Karin Do Amaral Riske
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 15/07548-7 - New route for synthesis of conjugates peptide-chitosan: the effects of the peptide's hydrophobicity evaluated on model membranes interaction via zeta potential
Grantee:Thais Helena Costa Petrin
Support Opportunities: Scholarships in Brazil - Scientific Initiation
FAPESP's process: 12/02065-0 - Electrophysiology of antimicrobial peptides in planar lipid bilayers
Grantee:Manoel de Arcisio Miranda Filho
Support Opportunities: Regular Research Grants
FAPESP's process: 12/24259-0 - Peptide and chitosan conjugates with pharmacological potential: synthesis, prospecting of activity in membrane mimetic systems, and evaluation in cells
Grantee:Marcia Perez dos Santos Cabrera
Support Opportunities: Research Grants - Young Investigators Grants