Literature DB >> 14705964

Kinetic analysis of ligand-induced autocatalytic reactions.

Jiang-Hong Liu1, Zhi-Xin Wang.   

Abstract

Protein phosphorylation and limited proteolysis are two most common regulatory mechanisms involving the energy-dependent covalent modification of regulatory enzymes. In addition to modifying other proteins, many protein kinases and proteases catalyse automodification reactions (i.e. reactions in which the kinase or zymogen serves as its own substrate), and their activities are frequently regulated by other regulatory ligands. In the present study, a kinetic analysis of autocatalytic reaction modulated by regulatory ligands is presented. On the basis of the kinetic equation, a novel procedure is developed to evaluate the kinetic parameters of the reaction. As an example of an application of this method, the effects of calcium ions on the autoacatalytic activation of trypsinogen by trypsin is re-examined. The results indicate that the binding affinity for Ca2+-bound trypsinogen to trypsin is at least two orders of magnitude higher than that for Ca2+-free trypsinogen, and therefore that the effect of Ca2+ ions on K(m*) values for trypsinogen is very much greater than that for the model peptides. Based on the experimental results, one possible molecular mechanism has been proposed.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14705964      PMCID: PMC1224100          DOI: 10.1042/BJ20031365

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  22 in total

1.  The single calcium-binding site of crystallin bovin beta-trypsin.

Authors:  W Bode; P Schwager
Journal:  FEBS Lett       Date:  1975-08-01       Impact factor: 4.124

2.  Autophosphorylation kinetics of protein kinases.

Authors:  Zhi-Xin Wang; Jia-Wei Wu
Journal:  Biochem J       Date:  2002-12-15       Impact factor: 3.857

3.  Relief by modification of carboxylate groups of the calcium requirement for the activation of trypsinogen.

Authors:  T M Radhakrishnan; K A Walsh; H Neurath
Journal:  J Am Chem Soc       Date:  1967-06-07       Impact factor: 15.419

Review 4.  Pancreatic proteinases; their activation and the disturbances of this mechanism in man.

Authors:  B Hadorn
Journal:  Med Clin North Am       Date:  1974-11       Impact factor: 5.456

5.  The mechanism of activation of trypsinogen. The role of the four N-terminal aspartyl residues.

Authors:  J P Abita; M Delaage; M Lazdunski
Journal:  Eur J Biochem       Date:  1969-04

6.  Comparative studies on the mechanism of activation of the two human trypsinogens.

Authors:  E Colomb; C Figarella
Journal:  Biochim Biophys Acta       Date:  1979-12-07

7.  On the activation of trypsinogen. A study of peptide models related to the N-terminal sequence of the zymogen.

Authors:  M Delaage; P Desnuelle; M Lazdunski; E Bricas; J Savrda
Journal:  Biochem Biophys Res Commun       Date:  1967-10-26       Impact factor: 3.575

8.  Sulfatide-dependent autoactivation of human blood coagulation Factor XII (Hageman Factor).

Authors:  G Tans; J Rosing; J H Griffin
Journal:  J Biol Chem       Date:  1983-07-10       Impact factor: 5.157

9.  Kinetic studies at high pH of the trypsin-catalyzed hydrolysis of N-alpha-benzoyl derivatives of L-arginamide, L-lysinamide, and S-2-aminoethyl-L-cysteinamide and related compounds.

Authors:  S S Wang; F H Carpenter
Journal:  J Biol Chem       Date:  1968-07-10       Impact factor: 5.157

10.  Structure of bovine trypsinogen at 1.9 A resolution.

Authors:  A A Kossiakoff; J L Chambers; L M Kay; R M Stroud
Journal:  Biochemistry       Date:  1977-02-22       Impact factor: 3.162

View more
  2 in total

Review 1.  Insights into the genetic risk factors for the development of pancreatic disease.

Authors:  Zachary Zator; David C Whitcomb
Journal:  Therap Adv Gastroenterol       Date:  2017-01-05       Impact factor: 4.409

Review 2.  Genetic risk factors for pancreatic disorders.

Authors:  David C Whitcomb
Journal:  Gastroenterology       Date:  2013-06       Impact factor: 22.682

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.