The full-length cDNA of anticoagulant protein infestin revealed a novel releasable Kazal domain, a neutrophil elastase inhibitor lacking anticoagulant activity

The full-length cDNA of anticoagulant protein infestin revealed a novel releasable Kazal domain, a neutrophil elastase inhibitor lacking anticoagulant activity

Author Lovato, Diogo Ventura Google Scholar
Nicolau de Campos, Ivan Torres Google Scholar
Amino, Rogerio Google Scholar
Tanaka, Aparecida Sadae Google Scholar
Institution Universidade Federal de São Paulo (UNIFESP)
Abstract Infestins are Kazal-type serine proteinase inhibitors found in the midgut of the Chagas' disease vector, Triatoma infestans. in previous studies, we characterized two double-headed infestins with potent anticoagulant activity; infestin 1-2, which inhibits thrombin and infestin 3-4, a factor XIIa inhibitor. in the present work, we have cloned the full-length cDNA of infestins' precursor. the translated cDNA predicted a polypeptide containing a signal peptide and seven Kazal-type domains, four domains from infestin 1-2 and infestin 3-4, and three new domains. Northern blot analysis confirmed that infestins are synthesized in a single transcript (similar to 1800 bp) in the insect midgut, but not in salivary glands. Based on the cDNA sequence, the three new Kazal domains were named infestin 1R, 2R and 3R. Infestin 2R-3R has 77% amino acid sequence identity to infestin 1-2 and the same basic amino acid residue at PI position in the inhibitory reactive site suggesting that these two proteins have a similar inhibitory specificity. in contrast, infestin IR has two different characteristics when compared to the other infestins: i) a hydrophobic amino acid residue at PI position in the inhibitory reactive site and ii) a prediction to be processed as a single Kazal domain, These two characteristics were experimentally demonstrated by the purification of native infestin I R from T infestans midgut. Native infestin I R was shown to be processed as a single Kazal domain by mass spectrometry and it was able to inhibit neutrophil elastase, subtilisin A and chymotrypsin. To further characterize infestin IR inhibitory activity, it was expressed as a recombinant protein in bacteria. Recombinant infestin IR inhibited neutrophil elastase with the same K-i of the native inhibitor. Moreover, it inhibited subtilisin A, chymotrypsin and proteinase K but did inhibit neither thrombin nor coagulation assays. in conclusion, unlike the other described infestins, infestin IR did not present anticoagulant activity and is processed as a single Kazal domain with inhibitory specificity towards proteases that hydrolyze peptide bonds after hydrophobic amino acid residues. (c) 2006 Elsevier SAS. All rights reserved.
Keywords serine proteinase inhibitor
multidomain
blood sucking
subtilisin inhibitor
elastase inhibitor
Triatoma infestans
Language English
Date 2006-06-01
Published in Biochimie. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 88, n. 6, p. 673-681, 2006.
ISSN 0300-9084 (Sherpa/Romeo, impact factor)
Publisher Elsevier B.V.
Extent 673-681
Origin http://dx.doi.org/10.1016/j.biochi.2005.11.011
Access rights Closed access
Type Article
Web of Science ID WOS:000239617600012
URI http://repositorio.unifesp.br/handle/11600/28944

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