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Peptide bioorthogonal functionality

In addition to the design principles just mentioned, peptides, proteins, and peptide-based supramolecular structures can be cross-linked into 3D networks via conventional synthetic chemistry (e.g., active ester chemistry or short synthetic cross-linkers) or via bioorthogonal click chemistry (e.g., Michael-type addition), utilizing their inherent multitude of functional groups (—NH, —COOH, —SH) and/or other additionally introduced functionalities. [Pg.217]


See other pages where Peptide bioorthogonal functionality is mentioned: [Pg.242]    [Pg.438]    [Pg.178]    [Pg.231]    [Pg.138]    [Pg.43]    [Pg.164]    [Pg.167]    [Pg.142]   
See also in sourсe #XX -- [ Pg.290 ]




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