Literature DB >> 924384

Isolation and characterisation of a low molecular weight inhibitor (of chymotrypsin and human granulocytic elastase and cathepsin G) from leeches.

U Seemüller, M Meier, K Ohlsson, H P Müller, H Fritz.   

Abstract

Two protein proteinase inhibitors were isolated and purified from the leech Hirudo medicinalis by means of gel filtration and ion-exchange chromatography. They inhibit chymotrypsin, subtilisin and the granulocytic neutral proteases elastase and cathepsin G. They proved to be homogeneous in polyacrylamide and dodecylsulfate gel electrophoresis and by end group analysis; only threonine was found as N-terminal amino acid residue using the dansylation technique. These inhibitors, which we call eglins, are stable in neutral and weakly acid (pH 3) solutions and resist non-specific proteolysis. From the amino acid compositions, a molecular weight of 6 600 - 6 800 is calculated for both inhibitory proteins, which is in good agreement with a value of about 6000 estimated by dodecylsulfate electrophoresis. The eglins contain an unusually large amount of hydrophobic amino acid residues but no methionine, isoleucine or--a rarity--cysteine residues or disulfide bridges. To our knowledge, the eglins are the first examples of proteinase inhibitors of the protein type which are not stabilized by disulfide bridges.

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Year:  1977        PMID: 924384     DOI: 10.1515/bchm2.1977.358.2.1105

Source DB:  PubMed          Journal:  Hoppe Seylers Z Physiol Chem        ISSN: 0018-4888


  14 in total

Review 1.  Small bite, large impact-saliva and salivary molecules in the medicinal leech, Hirudo medicinalis.

Authors:  Jan-Peter Hildebrandt; Sarah Lemke
Journal:  Naturwissenschaften       Date:  2011-11-09

2.  Kinetics of the interaction of chymotrypsin with eglin c.

Authors:  B Faller; J G Bieth
Journal:  Biochem J       Date:  1991-11-15       Impact factor: 3.857

3.  Prediction of location of active sites in biologically active peptides.

Authors:  T Kikuchi
Journal:  J Protein Chem       Date:  1996-08

4.  Long-range electrostatic complementarity governs substrate recognition by human chymotrypsin C, a key regulator of digestive enzyme activation.

Authors:  Jyotica Batra; András Szabó; Thomas R Caulfield; Alexei S Soares; Miklós Sahin-Tóth; Evette S Radisky
Journal:  J Biol Chem       Date:  2013-02-19       Impact factor: 5.157

5.  Inhibition of granulocyte-derived proteases reduces the increase in plasma endothelin associated with myocardial ischemia in the pig.

Authors:  T Tønnessen; A Ilebekk; P A Naess; G Christensen
Journal:  Basic Res Cardiol       Date:  1996 Jul-Aug       Impact factor: 17.165

6.  A large fragment approach to DNA synthesis: total synthesis of a gene for the protease inhibitor eglin c from the leech Hirudo medicinalis and its expression in E. coli.

Authors:  H Rink; M Liersch; P Sieber; F Meyer
Journal:  Nucleic Acids Res       Date:  1984-08-24       Impact factor: 16.971

7.  Kinetics of the inhibition of human leucocyte elastase by eglin from the leech Hirudo medicinalis.

Authors:  A Baici; U Seemüller
Journal:  Biochem J       Date:  1984-03-15       Impact factor: 3.857

Review 8.  Novel inhibitors of factor X for use in cardiovascular diseases.

Authors:  F A Spencer; R C Becker
Journal:  Curr Cardiol Rep       Date:  2000-09       Impact factor: 2.931

9.  Inhibition of human pancreatic proteinases by mucus proteinase inhibitor, eglin c and aprotinin.

Authors:  D Belorgey; S Dirrig; M Amouric; C Figarella; J G Bieth
Journal:  Biochem J       Date:  1996-01-15       Impact factor: 3.857

10.  In-vitro cleavage of a fusion protein bound to cellulose using the soluble yscFs (Kex2) variant.

Authors:  P G Seeboth; R A Warren; J Heim
Journal:  Appl Microbiol Biotechnol       Date:  1992-08       Impact factor: 4.813

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