The cyclotide family of circular miniproteins: Nature's combinatorial peptide template

• Published in: Biopolymers 2006, Vol.84 (3), p.250-266
• Main Authors: Craik, David J., Čemažar, Maša, Wang, Conan K. L., Daly, Norelle L.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Combinatorial Chemistry Techniques; Conserved Sequence; Cucurbitaceae; cyclic cystine knot; Cyclotides - chemistry; Cysteine - chemistry; Cystine Knot Motifs; Disulfides - chemistry; drug design; Hot Temperature; Human immunodeficiency virus; Hydrophobic and Hydrophilic Interactions; kalata B1; Models, Molecular; molecular scaffold; NMR structure determination; Nuclear Magnetic Resonance, Biomolecular; Peptides - chemistry; Plant Proteins - chemistry; Plant Proteins - genetics; Plant Proteins - metabolism; Protein Conformation; Protein Denaturation; Protein Structure, Secondary; Protein Structure, Tertiary; Rubiaceae; Templates, Genetic; Violaceae
• ISSN: 0006-3525; 1097-0282
• DOI: 10.1002/bip.20451

The cyclotides are a recently discovered family of miniproteins that contain a head‐to‐tail cyclized backbone and a knotted arrangement of disulfide bonds. They are approximately 30 amino acids in size and are present in high abundance in plants from the Violaceae, Rubiaceae, and Cucurbitaceae families, with individual plants containing a suite of up to 100 cyclotides. They have a diverse range of biological activities, including uterotonic, anti‐HIV, antitumor, and antimicrobial activities, although their natural function is likely that of defending their host plants from pathogens and pests. This review focuses on the structural aspects of cyclotides, which may be thought of as a natural combinatorial peptide template in which a wide range of amino acids is displayed on a compact molecular core made up of the cyclic cystine knot structural motif. Cyclotides are exceptionally stable and are resistant to denaturation via thermal, chemical, or enzymatic treatments. The structural features that contribute to their remarkable stability are described in this review. © 2006 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 84: 250–266, 2006 This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [e-mail]