Cargando…
Förster Resonance Energy Transfer Assay for Investigating the Reactivity of Thioesters in Biochemistry and Native Chemical Ligation
[Image: see text] Thioesters are considered to be “energy-rich” functional groups that are susceptible to attack by thiolate and amine nucleophiles while remaining hydrolytically stable at neutral pH, which enables thioester chemistry to take place in an aqueous medium. Thus, the inherent reactivity...
Autores principales: | Gless, Bengt H., Schmied, Sabrina H., Bejder, Benjamin S., Olsen, Christian A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207088/ https://www.ncbi.nlm.nih.gov/pubmed/37234128 http://dx.doi.org/10.1021/jacsau.3c00095 |
Ejemplares similares
-
Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation
por: Elashal, Hader E., et al.
Publicado: (2017) -
Native N-glycopeptide thioester synthesis through N→S acyl transfer
por: Premdjee, Bhavesh, et al.
Publicado: (2011) -
HF‐Free Boc Synthesis of Peptide Thioesters for Ligation and Cyclization
por: Raz, Richard, et al.
Publicado: (2016) -
Building photoswitchable 3,4'-AMPB peptides: Probing chemical ligation methods with reducible azobenzene thioesters
por: Zeyat, Gehad, et al.
Publicado: (2012) -
Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer
por: Macmillan, Derek, et al.
Publicado: (2011)