[引用][C] Synthesis of cyclic peptides through an intramolecular amide bond rearrangement

D Macmillan, M De Cecco, NL Reynolds… - …, 2011 - Wiley Online Library
The amide linkage is generally considered to make amides the most stable carboxylic acid
derivatives, and this is one feature that contributes to their attractiveness as building blocks …

Engineering of a linear inactive analog of human β‐defensin 4 to generate peptides with potent antimicrobial activity

H Sharma, B Mathew, R Nagaraj - Journal of Peptide Science, 2015 - Wiley Online Library
Human β‐defensins (HBDs) are cationic antimicrobial peptides constrained by three
disulfide bridges. They have diverse range of functions in the innate immune response. It is …

Linear analogues of human β‐defensin 3: concepts for design of antimicrobial peptides with reduced cytotoxicity to mammalian cells

S Liu, L Zhou, J Li, A Suresh, C Verma, YH Foo… - …, 2008 - Wiley Online Library
A series of engineered linear analogues [coded as F6, W6, Y6, A6, S6 and C (Acm) 6] were
modeled, designed, synthesized and structurally characterized by mass spectra, circular …

Cyclic peptides as novel therapeutic microbicides: engineering of human defensin mimetics

A Falanga, E Nigro, MG De Biasi, A Daniele, G Morelli… - Molecules, 2017 - mdpi.com
Cyclic peptides are receiving significant attention thanks to their antimicrobial activity and
high serum stability, which is useful to develop and design novel antimicrobial agents …

Design and activity of a cyclic mini-β-defensin analog: A novel antimicrobial tool

O Scudiero, E Nigro, M Cantisani… - International Journal …, 2015 - Taylor & Francis
We have designed a cyclic 17-amino acid β-defensin analog featuring a single disulfide
bond. This analog, designated “AMC”(ie, antimicrobial cyclic peptide), combines the internal …

Proteolytic degradation of reduced human beta defensin 1 generates a novel antibiotic octapeptide

J Wendler, BO Schroeder, D Ehmann, L Koeninger… - Scientific reports, 2019 - nature.com
Microbial resistance against clinical used antibiotics is on the rise. Accordingly, there is a
high demand for new innovative antimicrobial strategies. The host-defense peptide human …

Peptide fragments of a β-defensin derivative with potent bactericidal activity

NL Reynolds, M De Cecco, K Taylor… - Antimicrobial agents …, 2010 - Am Soc Microbiol
ABSTRACT β-Defensins are known to be both antimicrobial and able to chemoattract
various immune cells. Although the sequences of paralogous genes are not highly …

Peptide and protein thioester synthesis via N→ S acyl transfer

J Kang, D Macmillan - Organic & Biomolecular Chemistry, 2010 - pubs.rsc.org
Peptide and protein thioesters are playing an increasingly prominent role in the chemical
toolbox for protein assembly and modification through Native Chemical Ligation (NCL). In …

From protein total synthesis to peptide transamidation and metathesis: playing with the reversibility of N, S-acyl or N, Se-acyl migration reactions

O Melnyk, V Agouridas - Current Opinion in Chemical Biology, 2014 - Elsevier
Highlights•Reversible covalent chemistry and peptide dynamic combinatorial libraries.•
Chemoselective reversible amide bond and peptide bond forming reactions.•Peptide …

An optimized Fmoc synthesis of human defensin 5

E Vernieri, J Valle, D Andreu, BG de la Torre - Amino Acids, 2014 - Springer
Abstract Human α-defensin 5 (DEF5), expressed by the Paneth cells of human small
intestine, plays an important role in host defense against microbial infections. DEF5, a 32 …