Intracellular delivery of full length recombinant human mitochondrial L-Sco2 protein into the mitochondria of permanent cell lines and SCO2 deficient patient's primary cells-Reference-Cited by-同舟云学术

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Intracellular delivery of full length recombinant human mitochondrial L-Sco2 protein into the mitochondria of permanent cell lines and SCO2 deficient patient's primary cells

Published:2010-06 Issue:6 Volume:1802 Page:497-508
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Foltopoulou Parthena F.,Tsiftsoglou Asterios S.,Bonovolias Ioannis D.,Ingendoh Alexandra T.,Papadopoulou Lefkothea C.

Funder

Greek Ministry of Education

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference45 articles.

1. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene;Papadopoulou;Nat. Genet.,1999

2. Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig–Hoffmann disease;Salviati;Arch. Neurol.,2002

3. Human recombinant mutated forms of the mitochondrial COX assembly Sco2 protein differ from wild-type in physical state and copper binding capacity;Foltopoulou;Mol. Genet. Metab.,2004

4. Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts;Jaksch;Hum. Mol. Genet.,2001

5. Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase “assembly” protein;Williams;J. Biol. Chem.,2005

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