Американское общество гирудотерапии

Production, Purification, and Characterization of a Novel Cysteine-Rich Anticoagulant from the Medicinal Leech and the Functional Role of Its Disulfide Bonds

Basic science / preclinical published in Biomolecules (2025)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: In vitro / laboratoryГеномика и протеомикаФармакология секрета слюнных желёзРазработка лекарственных препаратовManuvera VA et al. · Biomolecules, 2025

Abstract

The saliva of the medicinal leech Hirudo medicinalis contains a wide range of biologically active compounds, including multiple anticoagulants. Previously, we identified a novel cysteine-rich anticoagulant protein (CRA) from leech saliva and produced it recombinantly in Escherichia coli, demonstrating its potential as a basis for new anticoagulant drugs. In this study, we developed an optimized procedure for scalable production and purification of recombinant CRA. The purified protein was analyzed for common contaminants originating from E. coli, such as endotoxins, bacterial proteins, and DNA, and its anticoagulant properties were evaluated using standard clotting assays. Across three independent experiments, the yield of purified CRA ranged from 3.7 to 5.5 mg per liter of bacterial culture, with impurity levels per milligram of protein ranging from 7.1-31.2 ng of bacterial proteins, 1.2-15.1 ng of DNA, and 60-1445 EU of endotoxins. The purified CRA displayed electrophoretic and chromatographic homogeneity and retained strong anticoagulant activity. Additionally, a truncated form of CRA lacking the C-terminal region was produced and characterized. This variant lost membrane affinity and showed altered activity profiles, with higher thrombin time activity but reduced prothrombin time and activated partial thromboplastin time activities compared with the full-length protein.

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 termsAnimalsAnticoagulantsHirudo medicinalisRecombinant ProteinsCysteineEscherichia coliLeechesBlood CoagulationSaliva

Резюме

Production, purification, and characterization of a novel cysteine-rich anticoagulant (CRA) from Hirudo medicinalis salivary secretions — a distant homolog of antistasin. The study describes recombinant expression in E. coli, refolding, and clotting-assay verification, with structural analysis of disulfide bonds essential for activity.

Почему это важно для гирудотерапии

The study reports an optimized procedure for producing and purifying recombinant cysteine-rich anticoagulant protein from medicinal leech Hirudo medicinalis saliva in Escherichia coli, including contaminant assessment and clotting-assay characterization. It found purified protein yields of 3.7 to 5.5 mg per liter of culture, measured impurity ranges for bacterial proteins, DNA, and endotoxins, electrophoretic and chromatographic homogeneity, and retained anticoagulant activity; a C-terminal-truncated variant lost membrane affinity and showed altered thrombin time, prothrombin time, and activated partial thromboplastin time activity profiles. This is directly relevant to ASH because it concerns a leech-saliva anticoagulant and its potential as a drug-development lead. The caveat is that the work is biochemical and preclinical, with no animal or human therapeutic data and no evaluation of live leech therapy.

Цитирование

Production, Purification, and Characterization of a Novel Cysteine-Rich Anticoagulant from the Medicinal Leech and the Functional Role of Its Disulfide Bonds.

Manuvera VA et al. · Biomolecules, 2025

Связанный клинический контекст

Добавлено в библиотеку ASH: May 27, 2026 · Последнее обновление сайта: June 18, 2026

Этот сайт предоставляет образовательную информацию и не является медицинской консультацией, диагнозом или рекомендацией по лечению. Гирудотерапия сопряжена с клинически значимыми рисками и должна проводиться только квалифицированными клиницистами в рамках институционально утверждённых протоколов. Разрешение FDA 510(k) для медицинских пиявок ограничено определёнными показаниями; обсуждения исследовательского и нелицензионного применения отмечены соответствующим образом. Для индивидуальных медицинских рекомендаций обратитесь к квалифицированному медицинскому специалисту.