Cargando…
Activation of cell-penetrating peptide fragments by disulfide formation
Three cell-penetrating peptides (CPPs), Tat, Pep-3 and penetratin, were split into two parts and each fragment was terminated with a cysteine residue, to allow disulfide bridge formation, as well as a fluorescent label, for visualization and quantitative analysis. After disulfide formation between t...
Autores principales: | Tooyserkani, Raheleh, Lipiński, Wojciech, Willemsen, Bob, Löwik, Dennis W. P. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497323/ https://www.ncbi.nlm.nih.gov/pubmed/32737661 http://dx.doi.org/10.1007/s00726-020-02880-x |
Ejemplares similares
-
Delivery of Various Cargos into Cancer Cells and Tissues via Cell-Penetrating Peptides: A Review of the Last Decade
por: Shoari, Alireza, et al.
Publicado: (2021) -
Activatable cell-penetrating peptides: 15 years of research
por: de Jong, Heleen, et al.
Publicado: (2020) -
Fragment synthesis of disulfide-containing peptides
por: Dai, Yuxuan, et al.
Publicado: (2020) -
Click to enter: activation of oligo-arginine cell-penetrating peptides by bioorthogonal tetrazine ligations
por: Bode, Saskia A., et al.
Publicado: (2018) -
Cellular Disulfide Bond Formation in Bioactive Peptides and Proteins
por: Patil, Nitin A., et al.
Publicado: (2015)