Literature DB >> 8732759

Interaction of subtilisins with serpins.

T Komiyama1, H Grøn, P A Pemberton, G S Salvesen.   

Abstract

Serpins are well-characterized inhibitors of the chymotrypsin family serine proteinases. We have investigated the interaction of two serpins with members of the subtilisin family, proteinases that possess a similar catalytic mechanism to the chymotrypsins, but a totally different scaffold. We demonstrate that alpha 1 proteinase inhibitor inhibits subtilisin Carlsberg and proteinase K, and alpha 1 antichymotrypsin inhibits proteinase K, but not subtilisin Carlsberg. When inhibition occurs, the rate of formation and stability of the complexes are similar to those formed between serpins and chymotrypsin family members. However, inhibition of subtilisins is characterized by large partition ratios where more than four molecules of each serpin are required to inhibit one subtilisin molecule. The partition ratio is caused by the serpins acting as substrates or inhibitors. The ratio decreases as temperature is elevated in the range 0-45 degrees C, indicating that the serpins are more efficient inhibitors at high temperature. These aspects of the subtilisin interaction are all observed during inhibition of chymotrypsin family members by serpins, indicating that serpins accomplish inhibition of these two distinct proteinase families by the same mechanism.

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Year:  1996        PMID: 8732759      PMCID: PMC2143405          DOI: 10.1002/pro.5560050509

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  37 in total

1.  An x-ray crystallographic study of the binding of peptide chloromethyl ketone inhibitors to subtilisin BPN'.

Authors:  J D Robertus; R A Alden; J J Birktoft; J Kraut; J C Powers; P E Wilcox
Journal:  Biochemistry       Date:  1972-06-20       Impact factor: 3.162

2.  Subtilisin BPN': kinetic study with oligopeptides.

Authors:  K Morihara; T Oka; H Tsuzuki
Journal:  Arch Biochem Biophys       Date:  1970-06       Impact factor: 4.013

Review 3.  Human plasma proteinase inhibitors.

Authors:  J Travis; G S Salvesen
Journal:  Annu Rev Biochem       Date:  1983       Impact factor: 23.643

4.  Amino acid sequence at the reactive site of human alpha 1-antichymotrypsin.

Authors:  M Morii; J Travis
Journal:  J Biol Chem       Date:  1983-11-10       Impact factor: 5.157

5.  Human leukocyte granule elastase: rapid isolation and characterization.

Authors:  R J Baugh; J Travis
Journal:  Biochemistry       Date:  1976-02-24       Impact factor: 3.162

6.  Studies on inhibition of neutrophil cathepsin G by alpha 1-antichymotrypsin.

Authors:  P A Patston
Journal:  Inflammation       Date:  1995-02       Impact factor: 4.092

7.  Reaction of human chymase with reactive site variants of alpha 1-antichymotrypsin. Modulation of inhibitor versus substrate properties.

Authors:  N M Schechter; L M Jordan; A M James; B S Cooperman; Z M Wang; H Rubin
Journal:  J Biol Chem       Date:  1993-11-05       Impact factor: 5.157

8.  Kinetics of association of serine proteinases with native and oxidized alpha-1-proteinase inhibitor and alpha-1-antichymotrypsin.

Authors:  K Beatty; J Bieth; J Travis
Journal:  J Biol Chem       Date:  1980-05-10       Impact factor: 5.157

9.  Human alpha 1-proteinase inhibitor. Crystal structure analysis of two crystal modifications, molecular model and preliminary analysis of the implications for function.

Authors:  H Loebermann; R Tokuoka; J Deisenhofer; R Huber
Journal:  J Mol Biol       Date:  1984-08-15       Impact factor: 5.469

10.  Ovomucoid third domains from 100 avian species: isolation, sequences, and hypervariability of enzyme-inhibitor contact residues.

Authors:  M Laskowski; I Kato; W Ardelt; J Cook; A Denton; M W Empie; W J Kohr; S J Park; K Parks; B L Schatzley
Journal:  Biochemistry       Date:  1987-01-13       Impact factor: 3.162

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  6 in total

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Authors:  Mareke Brüning; Martina Lummer; Caterina Bentele; Marcel M W Smolenaars; Kees W Rodenburg; Hermann Ragg
Journal:  Biochem J       Date:  2007-01-01       Impact factor: 3.857

2.  Activation of pro-caspase-7 by serine proteases includes a non-canonical specificity.

Authors:  Q Zhou; G S Salvesen
Journal:  Biochem J       Date:  1997-06-01       Impact factor: 3.857

3.  A novel locust (Schistocerca gregaria) serine protease inhibitor with a high affinity for neutrophil elastase.

Authors:  Michèle Brillard-Bourdet; Ahmed Hamdaoui; Eric Hajjar; Christian Boudier; Nathalie Reuter; Laurence Ehret-Sabatier; Joseph G Bieth; Francis Gauthier
Journal:  Biochem J       Date:  2006-12-15       Impact factor: 3.857

4.  Non-canonical proteolytic activation of human prothrombin by subtilisin from Bacillus subtilis may shift the procoagulant-anticoagulant equilibrium toward thrombosis.

Authors:  Giulia Pontarollo; Laura Acquasaliente; Daniele Peterle; Roberta Frasson; Ilaria Artusi; Vincenzo De Filippis
Journal:  J Biol Chem       Date:  2017-07-06       Impact factor: 5.157

5.  A proprotein convertase-inhibiting serpin with an endoplasmic reticulum targeting signal from Branchiostoma lanceolatum, a close relative of vertebrates.

Authors:  Caterina Bentele; Olaf Krüger; Ulf Tödtmann; Mareke Oley; Hermann Ragg
Journal:  Biochem J       Date:  2006-05-01       Impact factor: 3.857

6.  alpha1-Antitrypsin Portland, a bioengineered serpin highly selective for furin: application as an antipathogenic agent.

Authors:  F Jean; K Stella; L Thomas; G Liu; Y Xiang; A J Reason; G Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1998-06-23       Impact factor: 12.779

  6 in total

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