Strategies employed in the design of antimicrobial peptides with enhanced proteolytic stability
Z Lai, X Yuan, H Chen, Y Zhu, N Dong, A Shan - Biotechnology Advances, 2022 - Elsevier
Due to the alarming developing rate of multidrug-resistant bacterial pathogens, the
development and modification of antimicrobial peptides (AMPs) are unprecedentedly active …
development and modification of antimicrobial peptides (AMPs) are unprecedentedly active …
Recent advances in the development of anti-infective peptoids
In the search for new sources of antimicrobials many researchers have investigated
antimicrobial peptides (AMPs) as templates for the design of innovative therapeutics …
antimicrobial peptides (AMPs) as templates for the design of innovative therapeutics …
Cooperative Intramolecular Hydrogen Bonding Strongly Enforces cis-Peptoid Folding
Sequence-defined peptoids, or N-substituted glycines, are an attractive class of bioispired
polymer due to their biostability and efficient synthesis. However, the de novo design of …
polymer due to their biostability and efficient synthesis. However, the de novo design of …
Strategies to Control the Cis‐Trans Isomerization of Peptoid Amide Bonds
Peptoids are oligomers of N‐substituted glycine units. They structurally resemble peptides
but, unlike natural peptides, the side chains of peptoids are present on the amide nitrogen …
but, unlike natural peptides, the side chains of peptoids are present on the amide nitrogen …
Peptide science: A “rule model” for new generations of peptidomimetics
Peptides have been heavily investigated for their biocompatible and bioactive properties.
Though a wide array of functionalities can be introduced by varying the amino acid …
Though a wide array of functionalities can be introduced by varying the amino acid …
Submonomer synthesis of peptoids containing trans-inducing N-imino-and N-alkylamino-glycines
The use of hydrazones as a new type of submonomer in peptoid synthesis is described,
giving access to peptoid monomers that are structure-inducing. A wide range of hydrazones …
giving access to peptoid monomers that are structure-inducing. A wide range of hydrazones …
Fluorinated aromatic monomers as building blocks to control α-peptoid conformation and structure
Peptoids are peptidomimetics of interest in the fields of drug development and biomaterials.
However, obtaining stable secondary structures is challenging, and designing these …
However, obtaining stable secondary structures is challenging, and designing these …
Incorporation of CF 3-pseudoprolines into polyproline type II foldamers confers promising biophysical features
C Cayrou, A Walrant, D Ravault, K Guitot… - Chemical …, 2024 - pubs.rsc.org
The development and the use of fluorinated polyproline-type II (PPII) foldamers are still
underexplored. Herein, trifluoromethyl pseudoprolines have been incorporated into …
underexplored. Herein, trifluoromethyl pseudoprolines have been incorporated into …
Reverse turn and loop secondary structures in stereodefined cyclic peptoid scaffolds
Controlling the network of intramolecular interactions encoded by N α-chiral side chains and
the equilibria between cis-and trans-amide junctions in cyclic peptoid architectures …
the equilibria between cis-and trans-amide junctions in cyclic peptoid architectures …
Bio-instructive materials on-demand–combinatorial chemistry of peptoids, foldamers, and beyond
CN Herlan, D Feser, U Schepers… - Chemical Communications, 2021 - pubs.rsc.org
Combinatorial chemistry allows for the rapid synthesis of large compound libraries for high
throughput screenings in biology, medicinal chemistry, or materials science. Especially …
throughput screenings in biology, medicinal chemistry, or materials science. Especially …