Literature DB >> 2203472

The role of contact sites between inner and outer mitochondrial membrane in energy transfer.

K Nicolay1, M Rojo, T Wallimann, R Demel, R Hovius.   

Abstract

Three functions have been suggested to be localized in contact sites between the inner and the outer membrane of mitochondria from mammalian cells: (i) transfer of energy from matrix to cytosol through the action of peripheral kinases; (ii) import of mitochondrial precursor proteins; and (iii) transfer of lipids between outer and inner membrane. In the contact site-related energy transfer a number of kinases localized in the periphery of the mitochondrion play a crucial role. Two examples of such kinases are relevant here: (i) hexokinase isoenzyme I which is capable of binding to the outer aspect of the outer membrane; and (ii) the mitochondrial isoenzyme of creatine kinase which is localized in the intermembrane space. Recently, evidence was presented that both hexokinase and creatine kinase are preferentially localized in contact sites (Adams, V. et al. (1989) Biochim. Biophys. Acta 981, 213-225). The aim of the present experiments was two-fold. First, to establish methods which enable the bioenergetic aspects of energy transfer mediated by kinases in contact sites to be measured. In these experiments emphasis was on hexokinase, while 31P-NMR was the major experimental technique. Second, we wanted to develop methods which can give insight into factors playing a role in the formation of contact sites involved in energy transfer. In the latter approach, mitochondrial creatine kinase was studied using monolayer techniques.

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Year:  1990        PMID: 2203472     DOI: 10.1016/0005-2728(90)90255-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  11 in total

Review 1.  Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis.

Authors:  T Wallimann; M Wyss; D Brdiczka; K Nicolay; H M Eppenberger
Journal:  Biochem J       Date:  1992-01-01       Impact factor: 3.857

Review 2.  Regulation and pharmacology of the mitochondrial permeability transition pore.

Authors:  Dmitry B Zorov; Magdalena Juhaszova; Yael Yaniv; H Bradley Nuss; Su Wang; Steven J Sollott
Journal:  Cardiovasc Res       Date:  2009-05-15       Impact factor: 10.787

3.  Binding of rat brain hexokinase to recombinant yeast mitochondria: effect of environmental factors and the source of porin.

Authors:  C Aflalo; H Azoulay
Journal:  J Bioenerg Biomembr       Date:  1998-06       Impact factor: 2.945

4.  Mitochondrial creatine kinase isoform expression does not correlate with its mode of action.

Authors:  K Anflous; V Veksler; P Mateo; F Samson; V Saks; R Ventura-Clapier
Journal:  Biochem J       Date:  1997-02-15       Impact factor: 3.857

Review 5.  Homologous and heterologous interactions between hexokinase and mitochondrial porin: evolutionary implications.

Authors:  J E Wilson
Journal:  J Bioenerg Biomembr       Date:  1997-02       Impact factor: 2.945

6.  Mitochondrial creatine kinase binding to phospholipid monolayers induces cardiolipin segregation.

Authors:  Ofelia Maniti; Marie-France Lecompte; Olivier Marcillat; Bernard Desbat; René Buchet; Christian Vial; Thierry Granjon
Journal:  Biophys J       Date:  2009-03-18       Impact factor: 4.033

7.  Cardiolipin synthesis is required to support human cholesterol biosynthesis from palmitate upon serum removal in Hela cells.

Authors:  Kristin D Hauff; Seok-Yong Choi; Michael A Frohman; Grant M Hatch
Journal:  Can J Physiol Pharmacol       Date:  2009-10       Impact factor: 2.273

8.  Structure of the mitochondrial creatine kinase octamer: high-resolution shadowing and image averaging of single molecules and formation of linear filaments under specific staining conditions.

Authors:  T Schnyder; H Gross; H Winkler; H M Eppenberger; T Wallimann
Journal:  J Cell Biol       Date:  1991-01       Impact factor: 10.539

Review 9.  Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes.

Authors:  Ya-Wen Lu; Steven M Claypool
Journal:  Front Genet       Date:  2015-02-03       Impact factor: 4.599

Review 10.  Altered Traffic of Cardiolipin during Apoptosis: Exposure on the Cell Surface as a Trigger for "Antiphospholipid Antibodies".

Authors:  Valeria Manganelli; Antonella Capozzi; Serena Recalchi; Michele Signore; Vincenzo Mattei; Tina Garofalo; Roberta Misasi; Mauro Degli Esposti; Maurizio Sorice
Journal:  J Immunol Res       Date:  2015-09-29       Impact factor: 4.818

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