New anticoagulant protein from medicinal leech
Discovery study published in Biochem Biophys Res Commun (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.
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
Diese Studie berichtet über die Entdeckung und In-vitro-Charakterisierung eines zuvor unbeschriebenen antikoagulatorischen Proteins aus dem Speichel medizinischer Blutegel, das mittels vorausgegangener Transkriptom-, Genom- und Proteomanalysen von Speicheldrüsenzellen des Blutegels identifiziert wurde. Das rekombinante, in E. coli exprimierte Protein, das zu Antistasin homolog ist (28 % Aminosäureidentität), zeigte im activated partial thromboplastin time assay (aPTT-Test) eine signifikant stärkere Gerinnungshemmung als rekombinantes Hirudin bei äquimolaren Konzentrationen, wies eine gewisse direkte Thrombinhemmung auf (wenn auch weniger potent als Hirudin) und ergab gemischte Resultate in Faktor-Xa-Assays. Für den Bereich der ASH ist dies in hohem Maße relevant, da es das bekannte Repertoire leech-sezernierter Antikoagulanzien über Hirudin hinaus erweitert und zusätzliches pharmakologisches Potenzial innerhalb des Blutegel-Sekretoms nahelegt. Allerdings stammen sämtliche Befunde ausschließlich aus In-vitro-Gerinnungsassays; es werden keine In-vivo-, tierexperimentellen oder klinischen Daten präsentiert, und die therapeutische Relevanz des Proteins ist gänzlich ungeklärt.
Zitation
New anticoagulant protein from medicinal leech.
Manuvera VA et al. · Biochemical and biophysical research communications, 2024
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