What is Cyclic Peptide?
Cyclic peptides are peptide chains with a cyclic structure, mostly composed of 5-14 amino acids, with a molecular weight of about 500-2000 Da. Cyclic peptides have several advantages over linear peptides. Linear peptides as drugs may be inherently unstable and have a high probability of intracellular proteolysis. Considering that the free acid and free amine are at both ends, they are also usually polar. Cyclization promotes intramolecular hydrogen bonding within the ring structure and reduces the external hydrogen bonding capacity of the molecule, which reduces the polarity of the molecule compared to the acyclic precursor and increases the membrane permeability of the compound. The two β-turn local secondary structures caused by cyclization also reduce polar surface area, which generally enhances cell permeability.
Cyclic peptides are usually produced by end-to-end, cephalic, or side-chain-to-side-chain cyclization reactions. Introducing cyclization can make the conformation of the peptide chain more stable, thereby increasing the binding affinity to the target protein and reducing nonspecific binding due to fewer alternative conformations. Reduced conformational flexibility reduces the chance of molecules fitting to protease catalytic sites and improves proteomic resistance. Intervention in protein-protein interaction (PPI) by forming larger interaction surfaces to improve peptide chain efficacy.
Cyclic peptide drugs targeting intracellular proteins
Romidepsin is a natural bicyclic peptide discovered in Chromobacterium violaceum (1994), containing a head-to-tail lactone cyclization and a pair of disulfide bonds, mainly produced by fermentation. Romidepsin, a histone deacetylase inhibitor (HDACi), was approved by the FDA in 2009 for cutaneous T-cell lymphoma (CTCL) that has received at least one systemic therapy, primarily as an antineoplastic drug. It is a prodrug in which disulfide is reduced to two mercaptols in the intracellular matrix that chelates zinc ions at the zinc-dependent active site of histone deacetylase (HDAC), thereby inhibiting histone deacetylase and inducing apoptosis.
Voclosporin has 11 residues, including 1 D-type amino acid, which is head and tail cyclization. The N-terminus of some amino acids is methylated by S-adenosine methionine. Volcyclosporine was obtained by optimizing cyclosporin A. Voclosporin has better efficacy and metabolic stability than cyclosporin A. As a novel best-in-class calcineurin inhibitor (CNI), voclosporin has a synergistic and dual mechanism of action: it stabilizes renal podocyte by inhibiting CALcineurin (CN), blocking IL-2 expression and T cell-mediated immune response.
Cyclic peptide drugs targeting extramembrane proteins
Ziconotide is a synthetic omega-MVIIA toxin isolated from the venom of Conus Magus. It contains 25 residues, of which six amino acids are cysteine, linked by three pairs of disulfide bonds. As a potent selective blocker of N-type calcium channels, Ziconotide was approved in 2004 for the treatment of severe chronic pain.
Linaclotide is an oral peptide composed of 14 amino acids developed in the 1990s and belongs to the Cyclic Guanosine Monophosphate (cGMP) regulatory peptide family. In 2012, linaclotide was approved by the FDA for the treatment of irritable bowel syndrome with constipation (IBS-C).
Pukanatide is an oral guanylate cyclase C(GC-C) agonist developed by Synergy that regulates acid and base ions in the gastrointestinal tract, inducing fluid transport into the gastrointestinal tract and increasing peristalsis. Pukanatide, a 16-amino acid analog of uranyin, is produced by replacing Human uranyin Asp3 with Glu3 and binds to guanylate cyclase C(GC-C) receptors at pH 5.0 (duodenum and proximal jejunum pH) bound by 2 pairs of disulfide bonds. On 2017-01-19, Plcanatide was first approved by the FDA for the treatment of gastrointestinal disorders such as constipated irritable bowel syndrome (IBS-C) and chronic idiopathic constipation (CIC).
Pasireotide is a second-generation analog of somatostatin, a naturally occurring inhibitory hormone that blocks the release of several other hormones by interacting with the somatostatin receptor (coupled to G protein), including growth hormone, thyroid-stimulating hormone (TSH), insulin, and glucagon. Compared with other somatostatin analogs, paretide has a 40-fold increase in affinity for somatostatin receptor 5. Pasireotide is a head-to-tail cyclized hexapeptide. Pasireotide has a higher binding affinity to the somatostatin receptors SSTR1, SSTR3, and SSTR5 than octreotide and lanreotide.
Lanretide is the first sustained-release, long-acting somatostatin octapeptide analog, which is produced by cyclization of a disulfide bond between cysteine and cysteine, and binds stronger to somatostatin receptors on adenohypophysial cells than octreotide. Studies have shown that lanreotide mainly acts through somatostatin receptor-2 and somatostatin receptor-5, with a strong affinity for peripheral somatostatin receptors and a weaker affinity for central receptors.
Vasopressin, discovered in 1928 and its sequence elucidated in 1951, is an antidiuretic hormone with nine amino acids, cyclized by a disulfide bond between Cys4 and Cys9.
Terisopressin is a synthetic, long-acting vasopressin analog that acts on the vasopressin receptors V1a, V1b, and V2. It is a prodrug that is degraded in vivo by endopeptidase to form lysine-vasopressin by removing the trisglycine residue at the N-terminal of the cyclic peptide, which is the main active metabolite and is further degraded in the liver, kidney, and other tissues. As a result, teripressin acts slowly but has a longer duration, with a half-life of 6hr, which is longer than that of vasopressin (10min), and is safer with fewer side effects.
Bremelanotide is a synthetic peptide molecule consisting of seven amino acids cycled between side chains Asp2 and Lys7 to form the lactam analog (α-MSH) of the alpha-melanocyte-stimulating hormone.
Setmelanotide is a disulfide-cyclized octapeptide that preferentially agonizes the melanocortin 4 receptor (MC4R) with an EC50 of 0.2 nM.
Antimicrobial Cyclic Peptides
Daptomycin is a cyclic lipopeptide antibiotic isolated from Streptomyces rosiana. It contains 13 residues, 2 of which are non-natural amino acids, and 10 of which form lactone rings through the side chain and C-terminal of Thr4.
Telavancin is a semi-synthetic vancomycin derivative, which is based on the vancomycin structure. It is obtained by chemical modification to introduce an aliphatic chain on the amino group of the sugar group and to introduce methylamine methyl phosphate on the seventh aromatic amino acid. Through modification, the binding force with the cell membrane and affinity with the antibacterial target is enhanced, and teravanin is a fast bactericidal antibiotic for injection.
Dalbavancin is a second-generation semi-synthetic lipoglycopeptide antibiotic that is more potent than vancomycin and inhibits bacterial cell wall synthesis. The vancomycin family of natural antimicrobial glycopeptides is highly modifiable heptapeptides in which 5 amino acids remain unchanged, while amino acids 1 and 3 are highly differentiated. The heptapeptide core is used to bind the C-terminal D-Ala-D-Ala of the peptidoglycan chain and the side chain functional groups are derived to improve the properties of the peptide molecule.
Oritavancin, a second-generation, semi-synthetic lipoglycopeptide, is derived from chloroeremomycin, an analog of vancomycin. Similar to vancomycin, it contains a core heptapeptide.
- Caspofungin, Micafungin and Anidulafungin
Capofungin, micafengin, and anifengin all belong to the cyclic hexaliphatic peptide family. They share the same cyclic peptide core structure and are cyclized by amidation between the n-end of the side chain of the first lysine residue and the c-end of the peptide chain, and all target the 1,3-β -glucan synthase in the cell wall for the synthesis of glucan. All three antifungal agents have clinical efficacy against invasive candidiasis and other forms of systemic mycosis.
Cyclic peptide drugs approved in the last two decades (2001-2021)