Cargando…
Subunit disassembly and inhibition of TNFα by a semi-synthetic bicyclic peptide
Macrocyclic peptides are potentially a source of powerful drugs, but their de novo discovery remains challenging. Here we describe the discovery of a high-affinity (K(d) = 10 nM) peptide macrocycle (M21) against human tumor necrosis factor-alpha (hTNFα), a key drug target in the treatment of inflamm...
Autores principales: | Luzi, Stefan, Kondo, Yasushi, Bernard, Elise, Stadler, Lukas K. J., Vaysburd, Marina, Winter, Greg, Holliger, Philipp |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378371/ https://www.ncbi.nlm.nih.gov/pubmed/25614525 http://dx.doi.org/10.1093/protein/gzu055 |
Ejemplares similares
-
Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
por: Vedaraman, Sitara, et al.
Publicado: (2021) -
Towards XNA nanotechnology: new materials from synthetic genetic polymers
por: Pinheiro, Vitor B., et al.
Publicado: (2014) -
Versatile
Synthetic Approach for Selective Diversification of Bicyclic Aza-Diketopiperazines
por: Péron, Florent, et al.
Publicado: (2018) -
Bicyclic Schellman
Loop Mimics (BSMs): Rigid Synthetic C-Caps
for Enforcing Peptide Helicity
por: Mi, Tianxiong, et al.
Publicado: (2023) -
Mutational and Combinatorial Control of Self-Assembling and Disassembling of Human Proteasome α Subunits
por: Sekiguchi, Taichiro, et al.
Publicado: (2019)