Cargando…
A mixed chirality α-helix in a stapled bicyclic and a linear antimicrobial peptide revealed by X-ray crystallography
The peptide α-helix is right-handed when containing amino acids with l-chirality, and left-handed with d-chirality, however mixed chirality peptides generally do not form α-helices unless a helix inducer such as the non-natural residue amino-isobutyric acid is used. Herein we report the first X-ray...
Autores principales: | Baeriswyl, Stéphane, Personne, Hippolyte, Di Bonaventura, Ivan, Köhler, Thilo, van Delden, Christian, Stocker, Achim, Javor, Sacha, Reymond, Jean-Louis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637766/ https://www.ncbi.nlm.nih.gov/pubmed/34977576 http://dx.doi.org/10.1039/d1cb00124h |
Ejemplares similares
-
To Fold or
Not to Fold: Diastereomeric Optimization
of an α-Helical Antimicrobial Peptide
por: Personne, Hippolyte, et al.
Publicado: (2023) -
Chemical space guided discovery of antimicrobial bridged bicyclic peptides against Pseudomonas aeruginosa and its biofilms
por: Di Bonaventura, Ivan, et al.
Publicado: (2017) -
Dipropylamine for
9-Fluorenylmethyloxycarbonyl
(Fmoc) Deprotection with Reduced Aspartimide Formation in Solid-Phase
Peptide Synthesis
por: Personne, Hippolyte, et al.
Publicado: (2023) -
Machine learning designs non-hemolytic antimicrobial peptides
por: Capecchi, Alice, et al.
Publicado: (2021) -
Stereorandomization as a Method to Probe Peptide Bioactivity
por: Siriwardena, Thissa N., et al.
Publicado: (2021)