Jump to content

Inhibitor cystine knot

Add links
From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by CitationCleanerBot (talk | contribs) at 14:27, 26 June 2018 (cleanup, removed stub tag). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

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.[1]

An inhibitor cystine knot (aka ICK or Knottin) is a protein structural motif containing three disulfide bridges. Knottins are one of three foldsin 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]

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) shares the motif but its topology is such that it is the bond between the first and fourth disulphide which threads through the loop.

Proteins which contain the ICK motif

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. doi:10.1371/journal.pone.0075334. PMC 3792974. PMID 24116036.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  2. ^ "Knots". Cyclotide.com. Retrieved 2018-03-13. {{cite web}}: Cite has empty unknown parameter: |dead-url= (help)
  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: official publication of the Federation of American Societies for Experimental Biology. 17 (12): 1765–1767. doi:10.1096/fj.02-1044fje. ISSN 1530-6860. PMID 12958203.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  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.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  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. "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.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Inhibitor_cystine_knot&oldid=847601447"