Discovery and pharmacophoric characterization of chemokine network inhibitors using phage-display, saturation mutagenesis and computational modelling
CC and CXC-chemokines are the primary drivers of chemotaxis in inflammation, but chemokine network redundancy thwarts pharmacological intervention. Tick evasins promiscuously bind CC and CXC-chemokines, overcoming redundancy. Here we show that short peptides that promiscuously bind both chemokine cl...
Hlavní autoři: | Vales, S, Kryukova, J, Chandra, S, Smagurauskaite, G, Payne, M, Clark, CJ, Hafner, K, Mburu, P, Denisov, S, Davies, G, Outeiral, C, Deane, CM, Morris, GM, Bhattacharya, S |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
Springer Nature
2023
|
Podobné jednotky
-
Discovery and pharmacophoric characterization of chemokine network inhibitors using phage-display, saturation mutagenesis and computational modelling
Autor: Serena Vales, a další
Vydáno: (2023-09-01) -
Deep generative design with 3D pharmacophoric constraints
Autor: Imrie, F, a další
Vydáno: (2021) -
Promoter analysis by saturation mutagenesis
Autor: Baliga Nitin
Vydáno: (2001-01-01) -
Pharmacophores and pharmacophore searches /
Autor: Langer, Thierry, a další
Vydáno: (2006) -
Hijacking Transposable Elements for Saturation Mutagenesis in Fungi
Autor: Sanne Schrevens, a další
Vydáno: (2021-04-01)