Inhibitor cystine knot

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Top: general schematic of the structure of a knottin. A macrocyclic knot is formed by the core of beta strands (arrows) and disulfide bonds (yellow connections between numbered cysteines). Knottins are differentiated from GFCKs by the connectivity of their cysteines. Bottom: The general structure is easily seen in this crystal structure of EETI II taken from the protein database (PDB: 2IT7). Knottin Structure.png
Top: general schematic of the structure of a knottin. A macrocyclic knot is formed by the core of beta strands (arrows) and disulfide bonds (yellow connections between numbered cysteines). Knottins are differentiated from GFCKs by the connectivity of their cysteines. Bottom: The general structure is easily seen in this crystal structure of EETI II taken from the protein database (PDB: 2IT7).
MCh-1: A plant inhibitor cystine knot peptide from Momordica charantia. PDB entry 2m2q. 2m2q.png
MCh-1: A plant inhibitor cystine knot peptide from Momordica charantia . PDB entry 2m2q .

An inhibitor cystine knot (also known as ICK or Knottin) is a protein structural motif containing three disulfide bridges. Knottins are one of three folds in the cystine knot motif; the other closely related knots are the growth factor cystine knot (GFCK) and the cyclic cystine knot (CCK; cyclotide). [2] Types include a) cyclic mobius, b) cyclic bracelet, c) acyclic inhibitor knottins. [3] Cystine knot motifs are found frequently in nature in a plethora of plants, animals, and fungi and serve diverse functions from appetite suppression to anti-fungal activity. [4]

Contents

Along with the sections of polypeptide between them, two disulfides form a loop through which the third disulfide bond (linking the 3rd and 6th cysteine in the sequence) passes, forming a knot. The motif is common in invertebrate toxins such as those from arachnids and molluscs. The motif is also found in some inhibitor proteins found in plants, but the plant and animal motifs are thought to be a product of convergent evolution. [5] The ICK motif is a very stable protein structure which is resistant to heat denaturation and proteolysis. [6] CK peptide components of venoms target voltage-gated ion channels but members of the family also act as antibacterial and haemolytic agents. [7] Plant ICK proteins are often protease inhibitors.

Knottins have high stability to pH, heat, and enzymes. Because of their stability and their favorable pharmacodynamic properties, knottins are becoming increasingly popular as protein engineering scaffolds. Moreover, engineered knottins have shown significant promise as therapeutics, imaging agents, and targeting agents for chemotherapy. [8]

The mammalian proteins Agouti signalling peptide and Agouti related peptide are the only known mammalian examples of this motif. Both are neuropeptides involved in cell signalling. The former is responsible for hair (fur) colouration.

The motif is similar to the cyclic cystine knot or cyclotide, but lacks the cyclisation of the polypeptide backbone which is present in the latter family. The growth factor cystine knot (GFCK) is similar to the ICK but its topology is such that it is the bond between the first and fourth disulfide which threads through the loop.

Proteins which contain the ICK motif

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References

  1. ↑ He, W. J.; Chan, L. Y.; Clark, R. J.; Tang, J.; Zeng, G. Z.; Franco, O. L.; Cantacessi, C.; Craik, D. J.; Daly, N. L.; Tan, N. H. (2013). Driscoll, Paul C (ed.). "Novel Inhibitor Cystine Knot Peptides from Momordica charantia". PLOS ONE. 8 (10): e75334. Bibcode:2013PLoSO...875334H. doi: 10.1371/journal.pone.0075334 . PMC   3792974 . PMID   24116036.
  2. ↑ "Knots". Cyclotide.com. Archived from the original on 2015-02-05. Retrieved 2018-03-13.
  3. ↑ Reinwarth, Molecules 17:12533 2012 http://www.mdpi.com/1420-3049/17/11/12533/htm
  4. ↑ Zhu, Shunyi; Darbon, Herve; Dyason, Karin; Verdonck, Fons; Tytgat, Jan (September 2003). "Evolutionary origin of inhibitor cystine knot peptides". FASEB Journal. 17 (12): 1765–1767. doi: 10.1096/fj.02-1044fje . ISSN   1530-6860. PMID   12958203. S2CID   1117887.
  5. ↑ Zhu, S.; Darbon, H.; Dyason, K.; Verdonck, F.; Tytgat, J. (2003). "Evolutionary origin of inhibitor cystine knot peptides". The FASEB Journal. 17 (12): 1765–1767. doi: 10.1096/fj.02-1044fje . PMID   12958203. S2CID   1117887.
  6. ↑ Daly, N. L.; Craik, D. J. (2011). "Bioactive cystine knot proteins". Current Opinion in Chemical Biology. 15 (3): 362–368. doi:10.1016/j.cbpa.2011.02.008. PMID   21362584.
  7. ↑ Craik, D. J.; Daly, N. L.; Waine, C. (2001). "The cystine knot motif in toxins and implications for drug design". Toxicon. 39 (1): 43–60. doi:10.1016/S0041-0101(00)00160-4. PMID   10936622.
  8. ↑ Kintzing, James R; Cochran, Jennifer R (2016). "Engineered knottin peptides as diagnostics, therapeutics, and drug delivery vehicles". Current Opinion in Chemical Biology. 34: 143–150. doi:10.1016/j.cbpa.2016.08.022. PMID   27642714.
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