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Thiol–Norbornene Photoclick Chemistry for Grafting Antimicrobial Peptides onto Chitosan to Create Antibacterial Biomaterials AITranslate

Universidade do Porto; Universidade do Porto; Universidade Nova de Lisboa; Universidade do Porto; Universidade do Porto; Universidade do Porto; Universidade do Porto; Universidade do Porto; Universidade do Porto; Universidade do Porto
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Publisher: ACS
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Abstract AITranslate

Covalent conjugation of antimicrobial peptides (AMP) is considered an effective approach to overcome their potential degradation in vivo. As the high cost of AMP-based therapies is one of the major hurdles toward their clinical application, it is urgently needed to explore high yield reactions. Herein, the highly efficient thiol–norbornene photoclick chemistry (TNPC) was explored for AMP grafting onto chitosan. Norbornenes were introduced onto chitosan (NorChit) in an aqueous/organic system, followed by UV-triggered conjugation of N- and C-terminus cysteine-modified Dhvar5 (NorChit-Dhvar5). Up to 0.38 norbornene groups per chitosan repeating unit and up to 43% conjugation yield in NorChit-Nt-Dhvar5 (80 μmol of Dhvar5/g) were achieved, while in NorChit-Ct-Dhvar5 conjugation yield was 30% (55 μmol of Dhvar5/g). Finally, NorChit-Dhvar5 ultrathin films showed up to a 35% reduction of total adhered Gram-positive Staphylococcus epidermidis and increased the adhesion and killing of Gram-negative Pseudomonas aeruginosa compared to unmodified chitosan. Moreover, NorChit-Dhvar5 was noncytotoxic to human neonatal dermal fibroblasts, according to ISO 10993-1. Overall, our findings indicate TNPC as a high yield strategy for AMP grafting onto norbornene-functionalized biopolymers toward the fabrication of antibacterial biomaterials.

KeyWords AITranslate

peptidopolysaccharides surface modification covalent conjugation thiol−ene peptide tethering Dhvar5
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.2c00563

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Citation Information:

Covalent conjugation of antimicrobial peptides (AMP) is considered an effective approach to overcome their potential degradation in vivo. As the high cost of AMP-based therapies is one of the major hurdles toward their clinical application, it is urgently needed to explore high yield reactions. Herein, the highly efficient thiol–norbornene photoclick chemistry (TNPC) was explored for AMP grafting onto chitosan. Norbornenes were introduced onto chitosan (NorChit) in an aqueous/organic system, followed by UV-triggered conjugation of N- and C-terminus cysteine-modified Dhvar5 (NorChit-Dhvar5). Up to 0.38 norbornene groups per chitosan repeating unit and up to 43% conjugation yield in NorChit-Nt-Dhvar5 (80 μmol of Dhvar5/g) were achieved, while in NorChit-Ct-Dhvar5 conjugation yield was 30% (55 μmol of Dhvar5/g). Finally, NorChit-Dhvar5 ultrathin films showed up to a 35% reduction of total adhered Gram-positive Staphylococcus epidermidis and increased the adhesion and killing of Gram-negative Pseudomonas aeruginosa compared to unmodified chitosan. Moreover, NorChit-Dhvar5 was noncytotoxic to human neonatal dermal fibroblasts, according to ISO 10993-1. Overall, our findings indicate TNPC as a high yield strategy for AMP grafting onto norbornene-functionalized biopolymers toward the fabrication of antibacterial biomaterials.

quote

GB/T 7714-2015 [1] Pedro M. Alves, Rúben F. Pereira, Beatriz Costa, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c00563.
MLA [1] Pedro M. Alves, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c00563.
APA [1] Pedro M. Alves, Rúben F. Pereira, Beatriz Costa, Natália Tassi, Cátia Teixeira, Victoria Leiro, Cláudia Monteiro, Paula Gomes, Fabíola Costa, & M. Cristina L. Martins. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c00563
IEEE [1] Pedro M. Alves, Rúben F. Pereira, Beatriz Costa, Natália Tassi, Cátia Teixeira, Victoria Leiro, Cláudia Monteiro, Paula Gomes, Fabíola Costa, and M. Cristina L. Martins, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c00563. keywords: {peptidopolysaccharides;surface modification;covalent conjugation;thiol−ene;peptide tethering;Dhvar5}