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Exploration of novel cationic amino acid-enriched short peptides: design, SPPS, biological evaluation and study
Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens. In this context, we explored the potential of cationic amino acid-enriched short peptides, synthesized via solid-phase methods, as inn...
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Published in: | RSC advances 2024-06, Vol.14 (25), p.1771-17723 |
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container_title | RSC advances |
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creator | Chandole, Prashant K Pawar, Tushar Janardan Olivares-Romero, José Luis Tivari, Sunil R Garcia Lara, Bianney Patel, Harun Ahmad, Iqrar Delgado-Alvarado, Enrique Kokate, Siddhant V Jadeja, Yashwantsinh |
description | Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens. In this context, we explored the potential of cationic amino acid-enriched short peptides, synthesized
via
solid-phase methods, as innovative antimicrobial candidates. Our comprehensive evaluation assessed the antibacterial and antifungal efficacy of these peptides against a panel of significant pathogens, including
Escherichia coli
,
Pseudomonas aeruginosa
,
Staphylococcus aureus
,
Streptococcus pyogenes
,
Candida albicans
, and
Aspergillus niger
. Utilizing molecular docking techniques, we delved into the molecular interactions underpinning the peptides' action against these microorganisms. The results revealed a spectrum of inhibitory activities, with certain peptide sequences displaying pronounced effectiveness across various pathogens. These findings underscore the peptides' potential as promising antimicrobial agents, with molecular docking offering valuable insights into their mechanisms of action. This study enriches antimicrobial peptide (AMP) research by identifying promising candidates for further refinement and development toward therapeutic application, highlighting their significance in addressing the urgent issue of AMR.
Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens. |
doi_str_mv | 10.1039/d3ra08313f |
format | article |
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via
solid-phase methods, as innovative antimicrobial candidates. Our comprehensive evaluation assessed the antibacterial and antifungal efficacy of these peptides against a panel of significant pathogens, including
Escherichia coli
,
Pseudomonas aeruginosa
,
Staphylococcus aureus
,
Streptococcus pyogenes
,
Candida albicans
, and
Aspergillus niger
. Utilizing molecular docking techniques, we delved into the molecular interactions underpinning the peptides' action against these microorganisms. The results revealed a spectrum of inhibitory activities, with certain peptide sequences displaying pronounced effectiveness across various pathogens. These findings underscore the peptides' potential as promising antimicrobial agents, with molecular docking offering valuable insights into their mechanisms of action. This study enriches antimicrobial peptide (AMP) research by identifying promising candidates for further refinement and development toward therapeutic application, highlighting their significance in addressing the urgent issue of AMR.
Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens.</description><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d3ra08313f</identifier><ispartof>RSC advances, 2024-06, Vol.14 (25), p.1771-17723</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Chandole, Prashant K</creatorcontrib><creatorcontrib>Pawar, Tushar Janardan</creatorcontrib><creatorcontrib>Olivares-Romero, José Luis</creatorcontrib><creatorcontrib>Tivari, Sunil R</creatorcontrib><creatorcontrib>Garcia Lara, Bianney</creatorcontrib><creatorcontrib>Patel, Harun</creatorcontrib><creatorcontrib>Ahmad, Iqrar</creatorcontrib><creatorcontrib>Delgado-Alvarado, Enrique</creatorcontrib><creatorcontrib>Kokate, Siddhant V</creatorcontrib><creatorcontrib>Jadeja, Yashwantsinh</creatorcontrib><title>Exploration of novel cationic amino acid-enriched short peptides: design, SPPS, biological evaluation and study</title><title>RSC advances</title><description>Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens. In this context, we explored the potential of cationic amino acid-enriched short peptides, synthesized
via
solid-phase methods, as innovative antimicrobial candidates. Our comprehensive evaluation assessed the antibacterial and antifungal efficacy of these peptides against a panel of significant pathogens, including
Escherichia coli
,
Pseudomonas aeruginosa
,
Staphylococcus aureus
,
Streptococcus pyogenes
,
Candida albicans
, and
Aspergillus niger
. Utilizing molecular docking techniques, we delved into the molecular interactions underpinning the peptides' action against these microorganisms. The results revealed a spectrum of inhibitory activities, with certain peptide sequences displaying pronounced effectiveness across various pathogens. These findings underscore the peptides' potential as promising antimicrobial agents, with molecular docking offering valuable insights into their mechanisms of action. This study enriches antimicrobial peptide (AMP) research by identifying promising candidates for further refinement and development toward therapeutic application, highlighting their significance in addressing the urgent issue of AMR.
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via
solid-phase methods, as innovative antimicrobial candidates. Our comprehensive evaluation assessed the antibacterial and antifungal efficacy of these peptides against a panel of significant pathogens, including
Escherichia coli
,
Pseudomonas aeruginosa
,
Staphylococcus aureus
,
Streptococcus pyogenes
,
Candida albicans
, and
Aspergillus niger
. Utilizing molecular docking techniques, we delved into the molecular interactions underpinning the peptides' action against these microorganisms. The results revealed a spectrum of inhibitory activities, with certain peptide sequences displaying pronounced effectiveness across various pathogens. These findings underscore the peptides' potential as promising antimicrobial agents, with molecular docking offering valuable insights into their mechanisms of action. This study enriches antimicrobial peptide (AMP) research by identifying promising candidates for further refinement and development toward therapeutic application, highlighting their significance in addressing the urgent issue of AMR.
Antimicrobial resistance (AMR) represents a critical challenge worldwide, necessitating the pursuit of novel approaches to counteract bacterial and fungal pathogens.</abstract><doi>10.1039/d3ra08313f</doi><tpages>14</tpages></addata></record> |
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title | Exploration of novel cationic amino acid-enriched short peptides: design, SPPS, biological evaluation and study |
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