Orthogonal ligation strategies for peptide and protein

• Published in: Biopolymers Vol. 51; no. 5; pp. 311 - 332
• Main Authors: Tam, James P., Yu, Qitao, Miao, Zhenwei
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 1999
• Subjects: Amino Acids - metabolism; Ligands; Peptide Biosynthesis; Peptides - chemical synthesis; Peptides - metabolism; Protein Engineering - methods; Proteins - chemical synthesis; Proteins - metabolism
• ISSN: 0006-3525; 1097-0282
• DOI: 10.1002/(SICI)1097-0282(1999)51:5<311::AID-BIP2>3.0.CO;2-A

This review focuses on the concept, criteria, and methods of an orthogonal amide ligating strategy suitable for syntheses of peptides, peptide mimetics, and proteins. Utilizing unprotected peptides or proteins derived from chemical or biosynthetic sources, this ligation strategy has been shown to be general and exceptionally mild. Its orthogonality in ligating two unprotected segments with free N‐terminal (NT)‐amines at a specific NT‐amine is achieved through a chemoselective capture step and then an intramolecular acyl transfer reaction. Both coupling reagents for enthalpic activation and protection schemes therefore become unnecessary. More than a dozen orthogonal ligation methods based on either imine or thioester captures have been developed to afford native and unusual amino acids at ligation sites of linear, branched, or cyclic peptides. Because unprotected peptides and proteins of different sizes and forms can be obtained from either chemical or recombinant sources, orthogonal ligation removes the size limitation imposed on the chemical synthesis of a protein with a native or non‐native structure. Furthermore, by using building blocks from biosynthetic sources, orthogonal ligation provides a unifying operational concept for both total and semisynthesis of peptides and proteins. © 2000 John Wiley & Sons, Inc. Biopoly 51: 311–332, 1999