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Cyclic Peptide Synthesis

Cyclic peptides are a class of compounds with improved biological activities ranging from antibiotics to immunosuppressant drugs and toxins. They are much more resistant to enzyme degradation than non-cyclic peptide chains and are able to bind drug targets in vivo. These cyclic peptides can be modified using several approaches to enhance peptide stability such as N- and C-terminal capping, D-amino acids, side chain modifications, unique amino acids, N-alkylation of amide nitrogen and cyclization.

Selleck provides the synthesis of different types of cyclic peptides as indicated in the following:

1. Head-to-tail cyclized peptide: this is where the entire amino acid sequence is involved in the cyclization structure.
2. One or more cycles per peptide: this is where a part of the sequence is involved in the formation of the cycle(s).
3. Cycles can be formed either by an amide bond or disulfide (-SS-) bridge formed between two residues of amino acids (cysteine or penicilamine).

e.g. NIYNCEPANPSEKNSPSTQYCYSIQ

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