Amerikanische Gesellschaft für Hirudotherapie

Ornatins: potent glycoprotein IIb-IIIa antagonists and platelet aggregation inhibitors from the leech Placobdella ornata

Research article published in European journal of biochemistry (1991)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Observational studyGenomik & ProteomikMazur P et al. · European journal of biochemistry, 1991

Abstract

The purification and characterization of six isoforms of ornatin, potent glycoprotein IIb-IIIa (GP IIb-IIIa) antagonists and platelet aggregation inhibitors are described. These isoforms were purified from whole leech homogenates of the leech Placobdella ornata, a North American leech commonly known as the turtle leech, by trichloroacetic acid precipitation, Sephadex G-50 size exclusion chromatography, GP IIb-IIIa affinity chromatography, and C18 reverse-phase HPLC. Each of the five completely sequenced isoforms, which range from 41 to 52 residues in length, contains the Arg-Gly-Asp (RGD) sequence, a common recognition sequence in adhesion proteins, as well as 6 cysteine residues; the positions of both of these features are conserved in the primary sequences. The amino acid sequences of ornatin isoforms B, C, D, and E are highly conserved, whereas ornatin A2 and A3 are less similar and lack 9 residues at the N-terminus. The ornatins are approximately 40% identical with decorsin, a GP IIb-IIIa antagonist isolated from the leech Macrobdella decora [Seymour, J. L., Henzel, W. J., Nevins, B., Stults, J. T. & Lazarus, R. A. (1990) J. Biol. Chem. 265, 10143-10147]; furthermore, the RGD sequence and 5 out of 6 cysteine residues are maintained in the same relative positions in both decorsin and ornatin. The ornatin isoforms do not exhibit significant similarity to any members of the snake-venom-derived family of GP IIb-IIIa antagonists [Dennis, M. S., Henzel, W. J., Pitti, R. M., Lipari, M. T., Napier, M. A., Deisher, T. A., Bunting, S. & Lazarus, R. A. (1990) Proc. Natl Acad. Sci. USA 87, 2471-2475] except in the RGD region of these proteins. The ornatin isoforms inhibit the binding of GP IIb-IIIa to immobilized fibrinogen with IC50 values ranging over 2.9-5.3 nM; ornatin isoforms A2, C, and E inhibit ADP-induced human platelet aggregation with IC50 values of about 130, 280, and 440 nM, respectively.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeComparative StudyJournal Article
Indexed MeSH termsAmino Acid SequenceAnimalsChromatography, AffinityChromatography, GelChromatography, High Pressure LiquidHumansInvertebrate HormonesLeechesMolecular Sequence DataMolecular WeightPlatelet AggregationPlatelet Aggregation Inhibitors

Zusammenfassung

The purification and characterization of six isoforms of ornatin, potent glycoprotein IIb-IIIa (GP IIb-IIIa) antagonists and platelet aggregation inhibitors are described.

Warum dies für die Hirudotherapie relevant ist

This study purified and characterized six isoforms of ornatin — potent glycoprotein IIb-IIIa (GP IIb-IIIa) antagonists and platelet aggregation inhibitors — from whole-leech homogenates of Placobdella ornata (the North American turtle leech). The five fully sequenced isoforms (41–52 residues) each contain a conserved RGD motif and six cysteine residues, share approximately 40% identity with decorsin from Macrobdella decora, and inhibit fibrinogen binding to GP IIb-IIIa with IC50 values of 2.9–5.3 nM, with selected isoforms inhibiting ADP-induced human platelet aggregation at nanomolar-to-submicromolar concentrations. This is directly relevant to ASH's domain as a characterization of bioactive antiplatelet compounds from the leech secretome. The honest caveat is that this is an in vitro biochemical purification and characterization study with no in vivo or clinical data.

Zitation

Ornatins: potent glycoprotein IIb-IIIa antagonists and platelet aggregation inhibitors from the leech Placobdella ornata

Mazur P et al. · European journal of biochemistry, 1991

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