Literature DB >> 238839

The mitochondrial ATPase. Evidence for a single essential tyrosine residue.

S J Ferguson, W J Lloyd, M H Lyons, G K Radda.   

Abstract

1. Evidence is presented which indicates that inactivation of the mitochondrial ATPase from bovine heart by the reagent 4-chloro-7-nitrobenzofurazan results from modification of one tyrosine residue per enzyme molecule. Activity can be restored by a variety of sulphydryl reagents. 2. In sodium dodecyl sulphate, the nitrogenzofurazan group on tyrosine is transfered to newly exposed sulphydryl groups on the enzyme. 3. The rate of transfer of the nitrobenzofurazan moiety from theenzyme to sulphydryl compounds is compared with that for transfer from the model compound N-acetyl-tyrosine-0(7-nitrobenzo-furazan) ethyl ester, the synthesis and properties of which are also described. 4. The ligands ATP and ADP exert a protective effect on the rate of reaction between the mitochondrial ATPase and 4-chloro-7-nitrobenzofurazan. The variation in rate of this reaction with change in pH has also been examined and a pKa of 9.5 estimated for the tyrosine residue. 5. The modification does not prevent substrate binding as judged by changes in the fluorescence of aurovertin, an antibiotic with specific affinity for mitochondiral ATPases. 6. When the ATPase activity of submitochondrial particles is inhibited by 4-chloro-7-nitrobenzo-furazan, there is a parallel decrease in the extent of the energy-linked fluorescence enhancement of 1-anilino-naphthalene-8-sulphonate induced by ATP hydrolysis. Both ATPase activity and the fluorescence enhancement are restored by sluphydryl reagents.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 238839     DOI: 10.1111/j.1432-1033.1975.tb04120.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  24 in total

Review 1.  Functional sites in F1-ATPases: location and interactions.

Authors:  W S Allison; J M Jault; S Zhuo; S R Paik
Journal:  J Bioenerg Biomembr       Date:  1992-10       Impact factor: 2.945

Review 2.  ATP synthase and the actions of inhibitors utilized to study its roles in human health, disease, and other scientific areas.

Authors:  Sangjin Hong; Peter L Pedersen
Journal:  Microbiol Mol Biol Rev       Date:  2008-12       Impact factor: 11.056

Review 3.  Role of energy in oxidative phosphorylation.

Authors:  A Matsuno-Yagi; Y Hatefi
Journal:  J Bioenerg Biomembr       Date:  1988-08       Impact factor: 2.945

Review 4.  Molecular switch of F0F1-ATP synthase, G-protein, and other ATP-driven enzymes.

Authors:  H Noji; T Amano; M Yoshida
Journal:  J Bioenerg Biomembr       Date:  1996-10       Impact factor: 2.945

Review 5.  Chemical modification of active sites in relation to the catalytic mechanism of F1.

Authors:  J H Wang
Journal:  J Bioenerg Biomembr       Date:  1988-08       Impact factor: 2.945

Review 6.  The number of functional catalytic sites on F1-ATPases and the effects of quaternary structural asymmetry on their properties.

Authors:  R L Cross
Journal:  J Bioenerg Biomembr       Date:  1988-08       Impact factor: 2.945

7.  Fluorometric evidence for control of the activity of F1-adenosinetriphosphatase by ligand-induced conformation change.

Authors:  J H Wang
Journal:  J Bioenerg Biomembr       Date:  1986-04       Impact factor: 2.945

8.  Purification and Characterization of the Soluble F(1)-ATPase of Oat Root Mitochondria.

Authors:  S K Randall; Y Wang; H Sze
Journal:  Plant Physiol       Date:  1985-12       Impact factor: 8.340

Review 9.  Recent developments on structural and functional aspects of the F1 sector of H+-linked ATPases.

Authors:  P V Vignais; M Satre
Journal:  Mol Cell Biochem       Date:  1984       Impact factor: 3.396

10.  Functional importance of αIle-346 and αIle-348 in the catalytic sites of Escherichia coli ATP synthase.

Authors:  Chao Zhao; Hiba Syed; Sherif S Hassan; Vineet K Singh; Zulfiqar Ahmad
Journal:  Arch Biochem Biophys       Date:  2016-01-14       Impact factor: 4.013

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.