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1.
Parasitol Res ; 121(10): 2995-3006, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36006484

ABSTRACT

Haematophagous leeches express a broad variety of secretory proteins in their salivary glands, among them are hirudins and hirudin-like factors. Here, we describe the identification, molecular and initial functional characterization of Tandem-Hirudin (TH), a novel salivary gland derived factor identified in the Asian medicinal leech, Hirudinaria manillensis. In contrast to the typical structure of hirudins, TH comprises two globular domains arranged in a tandem-like orientation and lacks the elongated C-terminal tail. Similar structures of thrombin inhibitors have so far been identified only in kissing bugs and ticks. Expression of TH was performed in both cell-based and cell-free bacterial systems. A subsequent functional characterization revealed no evidence for a thrombin-inhibitory potency of TH.


Subject(s)
Hirudo medicinalis , Leeches , Amino Acid Sequence , Animals , Hirudins/metabolism , Hirudo medicinalis/metabolism , Leeches/chemistry , Thrombin
2.
Sci Rep ; 10(1): 19818, 2020 11 13.
Article in English | MEDLINE | ID: mdl-33188246

ABSTRACT

Synthesis and purification of peptide drugs for medical applications is a challenging task. The leech-derived factor hirudin is in clinical use as an alternative to heparin in anticoagulatory therapies. So far, recombinant hirudin is mainly produced in bacterial or yeast expression systems. We describe the successful development and application of an alternative protocol for the synthesis of active hirudin based on a cell-free protein synthesis approach. Three different cell lysates were compared, and the effects of two different signal peptide sequences on the synthesis of mature hirudin were determined. The combination of K562 cell lysates and the endogenous wild-type signal peptide sequence was most effective. Cell-free synthesized hirudin showed a considerably higher anti-thrombin activity compared to recombinant hirudin produced in bacterial cells.


Subject(s)
Hirudins/biosynthesis , Hirudo medicinalis/chemistry , Animals , Antithrombins , Cell-Free System/metabolism , Humans , K562 Cells , Recombinant Proteins/biosynthesis
3.
Parasitol Res ; 119(6): 1767-1775, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32363441

ABSTRACT

The hirudin-like factors 3 (HLF3) and 4 (HLF4) belong to a new class of leech-derived factors and are present in specimens of the three European medicinal leeches, Hirudo medicinalis, Hirudo verbana, and Hirudo orientalis, respectively. Here we describe the functional analysis of natural and synthetic variants of HLF3 and HLF4. Whereas the natural variants display only very low or no detectable anti-coagulatory activities, modifications within the N-termini in combination with an exchange of the central globular domain have the potency to greatly enhance the inhibitory effects of respective HLF3 and HLF4 variants on blood coagulation. Our results support previous observations on the crucial importance of all parts (both the N- and C-termini as well as the central globular domains) of hirudin and HLF molecules for thrombin inhibition.


Subject(s)
Hirudins/metabolism , Leeches/chemistry , Amino Acid Sequence , Animals , Blood Coagulation , Hirudins/chemistry , Hirudins/genetics , Hirudo medicinalis/chemistry , Hirudo medicinalis/genetics , Leeches/classification , Leeches/genetics , Protein Domains , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Structure-Activity Relationship , Thrombin/antagonists & inhibitors
4.
FEBS Lett ; 594(5): 841-850, 2020 03.
Article in English | MEDLINE | ID: mdl-31733150

ABSTRACT

The hirudin-like factor 1 (HLF1) of Hirudo medicinalis belongs to a new class of leech-derived factors. In previous investigations, HLF1 did not exhibit anticoagulatory activities. Here, we describe the analysis of natural and synthetic variants of HLF1 and HLF-Hyb, a yet uncharacterized member of the HLF family. Modifications within the N terminus of HLF1 have a strong impact on its activity. Some variants of HLF1 exhibit thrombin-inhibiting activity comparable to hirudins, whereas others have reduced or no activity. The analyses of HLF-Hyb variants revealed a strong impact of the central globular domain on activity. Our results indicate a comparable mode of action of hirudins and thrombin-inhibiting HLF variants. Finally, we propose and discuss criteria for classifying hirudins and HLFs.


Subject(s)
Hirudins/chemistry , Hirudins/metabolism , Leeches/metabolism , Animals , Hirudins/genetics , Humans , Leeches/chemistry , Leeches/genetics , Mutagenesis, Site-Directed , Protein Domains , Protein Engineering , Saliva/metabolism , Thrombin/metabolism
5.
Parasitol Res ; 118(7): 2223-2233, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31187225

ABSTRACT

Blood coagulation in vertebrates is a complex mechanism that involves the precisely coordinated and regulated action of a cascade of factors in order to prevent excessive blood loss upon wounding. Any blood sucking ectoparasite, however, has to circumvent this mechanism to ensure the uptake of an adequate blood meal. Inhibitors of blood coagulation in the saliva are hence widespread among these animals. Thrombin as a key factor of blood coagulation is a prominent target of such inhibitors, and hirudin is probably the best known among the thrombin inhibitors. Hirudin was originally described in the genus Hirudo, but occurs in other leech genera like Hirudinaria and Macrobdella as well. Besides several isoforms of hirudin, a new class of putative leech saliva components, the hirudin-like factors (HLFs), was identified in both genera Hirudo and Hirudinaria. Here, we describe the expression, purification, and functional characterization of three HLFs (HLF5, 6, and 8, respectively) and two additional hirudins (HM3 and HM4) of Hirudinaria manillensis. While HLF6 lacked any inhibitory activity on thrombin, HLF5 as well as HLF8 clearly exhibited anticoagulatory properties. The inhibitory activity of HLF5 and HLF8, however, was much lower compared with both HM3 and HM4 of Hirudinaria manillensis as well as the hirudin variants 1 (HV1) and 2 (HV2) of Hirudo medicinalis. Neither an inhibition of trypsin nor a platelet aggregation was caused by HLF8. Our data indicates the presence of two classes (rather than isoforms) of hirudins in Hirudinaria manillensis with markedly different inhibitory activity on human thrombin.


Subject(s)
Antithrombins/metabolism , Blood Coagulation/drug effects , Hirudins/metabolism , Hirudo medicinalis/metabolism , Thrombin/antagonists & inhibitors , Amino Acid Sequence , Animals , Humans , Recombinant Proteins/metabolism , Trypsin/metabolism
6.
J Parasitol ; 105(3): 423-431, 2019 06.
Article in English | MEDLINE | ID: mdl-31163003

ABSTRACT

Blood-sucking leeches, some of which are referred to as medicinal leeches, have caught attention not only because of their medical purposes, but also as study organisms to conduct research within fields as diverse as neurobiology, osmoregulation, ecology, and phylogeny. Of particular interest is the question whether hemophagy in leeches is of single origin or evolved independently several times. A key component in the saliva of hematophagous leeches is hirudin, a strong natural inhibitor of thrombin and hence the blood coagulation cascade. Multiple isoforms of hirudin have been described within and among several leech species and genera, often based on sequence data only. The identification of hirudin-like factors (HLFs) illustrated the necessity to underpin such predictions by functional tests. We overexpressed and purified the hirudin of the North American medicinal leech, Macrobdella decora, and proved its thrombin-inhibiting activity. In addition, analysis of the gene structure of both hirudin and some of the decorsins of M. decora clearly indicated conserved exon and intron positions when compared to genes of hirudins and HLFs of Eurasian medicinal leeches. Our data provide evidence for the incorporation of decorsins into the hirudin superfamily and support the concept of a single origin of blood feeding in jawed leeches.


Subject(s)
Cell Adhesion Molecules/genetics , Hirudins/genetics , Leeches/chemistry , Amino Acid Sequence , Animals , Asia , Blood Coagulation Tests , Cell Adhesion Molecules/chemistry , DNA, Complementary/chemistry , Europe , Exons , Genotyping Techniques , Hirudins/biosynthesis , Hirudins/chemistry , Hirudins/isolation & purification , Introns , Leeches/classification , Leeches/genetics , North America , Phylogeny , Salivary Glands/metabolism , Sequence Alignment
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