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Isolation and characterization of cotiaractivase, a novel low molecular weight prothrombin activator from the venom of Bothrops cotiara

Abstract:
In this study, we isolated a novel prothrombin activator from the venom of Bothrops cotiara, a Brazilian lance-headed pit viper (Cotiara, Jararaca preta, Biocotiara), which we have designated “cotiaractivase” (prefix: cotiar- from B. cotiara; suffix: -activase, from prothrombin activating activity). Cotiaractivase was purified using a phenyl-Superose hydrophobic interaction column followed by a Mono-Q anion exchange column. It is a single-chain polypeptide with a molecular weight of 22,931 Da as measured by mass spectroscopy. Cotiaractivase generated active α-thrombin from purified human prothrombin in a Ca2+-dependent manner as assessed by S2238 chromogenic substrate assay and SDS-PAGE. Cotiaractivase cleaved prothrombin at positions Arg271–Thr272 and Arg320–Ile321, which are also cleaved by factor Xa. However, the rate of thrombin generation by cotiaractivase was approximately 60-fold less than factor Xa alone and 17 × 106-fold less than the prothrombinase complex. The enzymatic activity of cotiaractivase was inhibited by the chelating agent EDTA, whereas the serine protease inhibitor PMSF had no effect on its activity, suggesting that it is a metalloproteinase. Interestingly, S2238 inhibited cotiaractivase activity non-competitively, suggesting that this toxin contains an exosite that allows it to bind prothrombin independently of its active site. Tandem mass spectrometry and N-terminal sequencing of purified cotiaractivase identified peptides that were identical to regions of the cysteine-rich and disintegrin-like domains of known snake venom metalloproteinases. Cotiaractivase is a unique low molecular weight snake venom prothrombin activator that likely belongs to the metalloproteinase family of proteins.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.bbapap.2006.03.004

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author


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Funder identifier:
https://ror.org/00cwqg982
Funding agency for:
García, A
Prabhakar, S
Zitzmann, N
More from this funder
Funding agency for:
García, A
Prabhakar, S
Zitzmann, N


Publisher:
Elsevier
Journal:
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics More from this journal
Volume:
1764
Issue:
5
Pages:
863-871
Publication date:
2006-04-07
Acceptance date:
2006-03-08
DOI:
EISSN:
1878-1454
ISSN:
0006-3002


Language:
English
Keywords:
Pubs id:
pubs:61026
UUID:
uuid:1744ba70-d3b0-4c5e-8e6f-b4c3861e6e8d
Local pid:
pubs:61026
Source identifiers:
61026
Deposit date:
2012-12-19
ARK identifier:

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