Amerikanische Gesellschaft für Hirudotherapie

New anticoagulant protein from medicinal leech

Discovery study published in Biochem Biophys Res Commun (2024)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: In vitro / laboratoryArzneimittelentwicklungSpeichel-PharmakologieManuvera VA et al. · Biochemical and biophysical research communications, 2024

Abstract

The saliva of the medicinal leech contains various anticoagulants. Some of them, such as hirudin, are well known. However, it is reasonable to believe that not all anticoagulant proteins from medicinal leech saliva have been identified. We previously performed a comprehensive study of the transcriptome, genome, and proteome of leech salivary gland cells, which led to the discovery of several previously unknown hypothetical proteins that may have anticoagulant properties. Subsequently, we obtained a series of recombinant proteins and investigated their impact on coagulation in in vitro assays. We identified a previously undescribed protein that exhibited a high ability to suppress coagulation. The His-tagged recombinant protein was expressed in Escherichia coli and purified using metal chelate chromatography. To determine its activity, commonly used coagulation methods were used: activated partial thromboplastin time, prothrombin time, and thrombin inhibition clotting assay. Clotting and chromogenic assays for factor Xa inhibition were performed to evaluate anti-Xa activity. We used recombinant hirudin as a control anticoagulant protein in all experiments. The new protein showed significantly greater inhibition of coagulation than hirudin at the same molar concentrations in the activated partial thrombin time assay. However, hirudin demonstrated better results in the direct thrombin inhibition test, although the tested protein also exhibited the ability to inhibit thrombin. The chromogenic analysis of factor Xa inhibition revealed no activity, whereas the clotting test for factor Xa showed the opposite result. Thus, a new powerful anticoagulant protein has been discovered in the medicinal leech. This protein is homologous to antistatin, with 28 % identical amino acid residues. The recombinant protein was expressed in E. coli. This protein is capable of directly inhibiting thrombin, and based on indirect evidence, other proteases of the blood coagulation cascade have been identified.

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

Publication typeJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAnticoagulantsHirudinsThrombinFactor XaEscherichia coliRecombinant Proteins

Zusammenfassung

Newly discovered medicinal leech anticoagulant protein homologous to antistasin (28% identity) with stronger aPTT inhibition than hirudin at equimolar concentrations; expressed in E. coli for evaluation.

Warum dies für die Hirudotherapie relevant ist

This study reports the discovery and in vitro characterization of a previously undescribed anticoagulant protein from medicinal leech saliva, identified through prior transcriptome, genome, and proteome analysis of leech salivary gland cells. The recombinant protein, expressed in E. coli and homologous to antistatin (28% amino acid identity), showed significantly greater coagulation inhibition than recombinant hirudin at equimolar concentrations in the activated partial thromboplastin time assay, exhibited some direct thrombin inhibition (though less potent than hirudin), and gave mixed results in factor Xa assays. For ASH's domain, this is highly relevant as it expands the known repertoire of leech-secreted anticoagulants beyond hirudin, suggesting additional pharmacological potential within the leech secretome. However, all findings are from in vitro coagulation assays only; no in vivo, animal, or clinical data are presented, and the protein's therapeutic relevance remains entirely unestablished.

Zitation

New anticoagulant protein from medicinal leech.

Manuvera VA et al. · Biochemical and biophysical research communications, 2024

Verwandter klinischer Kontext

Zur ASH-Bibliothek hinzugefügt: May 27, 2026 · Letzte Aktualisierung der Website: June 18, 2026

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