Natural antimicrobial peptides as inspiration for design of a new generation antifungal compounds
M Bondaryk, M Staniszewska, P Zielińska… - Journal of fungi, 2017 - mdpi.com
Invasive fungal infections are associated with high mortality rates, despite appropriate
antifungal therapy. Limited therapeutic options, resistance development and the high …
antifungal therapy. Limited therapeutic options, resistance development and the high …
[PDF][PDF] Antimicrobial peptides from frog skin: biodiversity and therapeutic promises
More than a thousand antimicrobial peptides (AMPs) have been reported in the last decades
arising from the skin secretion of amphibian species. Generally, each frog species can …
arising from the skin secretion of amphibian species. Generally, each frog species can …
Broad-spectrum antiviral activity of the amphibian antimicrobial peptide Temporin L and its analogs
C Zannella, A Chianese, L Palomba… - International Journal of …, 2022 - mdpi.com
The COVID-19 pandemic has evidenced the urgent need for the discovery of broad-
spectrum antiviral therapies that could be deployed in the case of future emergence of novel …
spectrum antiviral therapies that could be deployed in the case of future emergence of novel …
Customized reversible stapling for selective delivery of bioactive peptides
Z Zeng, J Zhu, X Deng, H Chen, Y Jin… - Journal of the …, 2022 - ACS Publications
We have developed a new concept for reversible peptide stapling that involves
macrocyclization between two amino groups and decyclization promoted via dual 1, 4 …
macrocyclization between two amino groups and decyclization promoted via dual 1, 4 …
Design, engineering and discovery of novel α-helical and β-boomerang antimicrobial peptides against drug resistant bacteria
S Bhattacharjya, SK Straus - International Journal of Molecular Sciences, 2020 - mdpi.com
In an era where the pipeline of new antibiotic development is drying up, the continuous rise
of multi-drug resistant (MDR) and extensively drug resistant (XDR) bacteria are genuine …
of multi-drug resistant (MDR) and extensively drug resistant (XDR) bacteria are genuine …
[HTML][HTML] Solution NMR studies of amphibian antimicrobial peptides: linking structure to function?
The high-resolution three-dimensional structure of an antimicrobial peptide has implications
for the mechanism of its antimicrobial activity, as the conformation of the peptide provides …
for the mechanism of its antimicrobial activity, as the conformation of the peptide provides …
First-in-class cyclic Temporin L analogue: Design, synthesis, and antimicrobial assessment
R Bellavita, B Casciaro, S Di Maro… - Journal of medicinal …, 2021 - ACS Publications
The pharmacodynamic and pharmacokinetic properties of bioactive peptides can be
modulated by introducing conformational constraints such as intramolecular …
modulated by introducing conformational constraints such as intramolecular …
[HTML][HTML] Binding of amphipathic α-helical antimicrobial peptides to lipid membranes: Lessons from temporins B and L
AK Mahalka, PKJ Kinnunen - Biochimica et Biophysica Acta (BBA) …, 2009 - Elsevier
Temporins constitute a family of amphipathic α-helical antimicrobial peptides (AMP) and
contain some of the shortest cytotoxic peptides, comprised of only 10–14 residues. General …
contain some of the shortest cytotoxic peptides, comprised of only 10–14 residues. General …
Membranolytic anticancer peptides
Membranolytic anticancer peptides (ACPs) potentially offer new perspectives for the
development of anticancer drugs. Their receptor-independent mechanisms of action hold …
development of anticancer drugs. Their receptor-independent mechanisms of action hold …
Selectivity of antimicrobial peptides: a complex interplay of multiple equilibria
S Bobone, L Stella - Antimicrobial Peptides: Basics for Clinical Application, 2019 - Springer
Antimicrobial peptides (AMPs) attack bacterial membranes selectively, killing microbes at
concentrations that cause no toxicity to the host cells. This selectivity is not due to interaction …
concentrations that cause no toxicity to the host cells. This selectivity is not due to interaction …