Spontaneous intermolecular amide bond formation between side chains for irreversible peptide targeting.
Peptides and synthetic peptide-like molecules are powerful tools for analysis and control of biological function. One major limitation of peptides is the instability of their interactions with biomolecules, because of the limited accessible surface area for noncovalent interactions and the intrinsic...
Główni autorzy: | Zakeri, B, Howarth, M |
---|---|
Format: | Journal article |
Język: | English |
Wydane: |
2010
|
Podobne zapisy
-
Peptide targeting by spontaneous isopeptide bond formation
od: Zakeri, B, i wsp.
Wydane: (2011) -
A peptide tag forming a spontaneous covalent bond applied to study forces at the mammalian cell surface
od: Fierer, J, i wsp.
Wydane: (2012) -
Development of spontaneous isopeptide bond formation for ligation of peptide tags
od: Fierer, JO
Wydane: (2014) -
Overcoming symmetry mismatch in vaccine nanoassembly via spontaneous amidation
od: Rahikainen, R, i wsp.
Wydane: (2020) -
Selective bi-directional amide bond cleavage of N-methylcysteinyl peptide
od: Qiu, Yibo, i wsp.
Wydane: (2014)