Titlebook: Enzyme-Mediated Ligation Methods; Timo Nuijens,Marcel Schmidt Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 2019

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Chemoenzymatic Synthesis of Linear- and Head-to-Tail Cyclic Peptides Using Omniligase-1,peptides. Reactions are irreversible and proceed with unprotected peptides (μM–mM concentration) in aqueous solution at slightly basic pH. Due to its high catalytic efficiency, only very low molar equivalents of omniligase-1 are required. In this chapter, a chemoenzymatic peptide synthesis (CEPS) ap

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Site-Specific Labeling of Proteins Using the Formylglycine-Generating Enzyme (FGE),directly from nature of introducing a unique amino acid into the larger context of a protein. Formylglycine (fGly) is a crucial component of the active site of sulfatases, where it directly participates in the breakdown of sulfate ester substrates. In the context of bioconjugation this aldehyde cont

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Butelase 1-Mediated Ligation of Peptides and Proteins,Asx) ligase activity and is virtually devoid of protease activity. Butelase 1 recognizes specifically a .-terminal Asx-containing tripeptide motif, Asx-His-Val, to form an Asx-Xaa peptide bond (Xaa = any amino acid), either intramolecularly or intermolecularly, resulting in cyclic peptides or site-s

Scleroderma

Trypsiligase-Catalyzed Peptide and Protein Ligation,sents a major challenge to protein chemists. Chemical labeling methods often target multiple positions within a protein and therefore suffer from a lack of specificity. Enzymatic protein modification is an attractive alternative due to the inherent regioselectivity and stereoselectivity of enzymes.

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SpyLigase-Catalyzed Modification of Antibodies,ifferent cell populations as well as for tracking intracellular pathways. In recent years, antibody–drug conjugates (ADCs) have emerged as promising therapeutics to treat cancer and have moved into the focus of interest of the pharmaceutical industry. Here we describe a conjugation method for the ge