Cargando…
Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents
Maleimides remain the reagents of choice for the preparation of therapeutic and imaging protein conjugates despite the known instability of the resulting products that undergo thiol-exchange reactions in vivo. Here we present the rational design of carbonylacrylic reagents for chemoselective cystein...
Autores principales: | Bernardim, Barbara, Cal, Pedro M.S.D., Matos, Maria J., Oliveira, Bruno L., Martínez-Sáez, Nuria, Albuquerque, Inês S., Perkins, Elizabeth, Corzana, Francisco, Burtoloso, Antonio C.B., Jiménez-Osés, Gonzalo, Bernardes, Gonçalo J. L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095172/ https://www.ncbi.nlm.nih.gov/pubmed/27782215 http://dx.doi.org/10.1038/ncomms13128 |
Ejemplares similares
-
Dichloro Butenediamides as Irreversible Site‐Selective Protein Conjugation Reagent
por: Laserna, Victor, et al.
Publicado: (2021) -
Quaternization of Vinyl/Alkynyl Pyridine Enables Ultrafast Cysteine‐Selective Protein Modification and Charge Modulation
por: Matos, Maria J., et al.
Publicado: (2019) -
Platform
for Orthogonal N-Cysteine-Specific
Protein Modification Enabled by Cyclopropenone Reagents
por: Istrate, Alena, et al.
Publicado: (2022) -
Chemo-
and Regioselective Lysine Modification on Native
Proteins
por: Matos, Maria J., et al.
Publicado: (2018) -
Enhancement of the Anti-Aggregation Activity of a
Molecular Chaperone Using a Rationally Designed Post-Translational
Modification
por: Lindstedt, Philip R., et al.
Publicado: (2019)