Your browser doesn't support javascript.
loading
Expression and processing of the TMEM70 protein.
Hejzlarová, Katerina; Tesarová, Markéta; Vrbacká-Cízková, Alena; Vrbacký, Marek; Hartmannová, Hana; Kaplanová, Vilma; Nosková, Lenka; Kratochvílová, Hana; Buzková, Jana; Havlícková, Vendula; Zeman, Jirí; Kmoch, Stanislav; Houstek, Josef.
Affiliation
  • Hejzlarová K; Institute of Physiology Academy of Sciences of the Czech Republic, 142 20 Prague, Czech Republic.
Biochim Biophys Acta ; 1807(1): 144-9, 2011 Jan.
Article in En | MEDLINE | ID: mdl-20937241
ABSTRACT
TMEM70 protein represents a novel ancillary factor of mammalian ATP synthase. We have investigated import and processing of this factor in human cells using GFP- and FLAG-tagged forms of TMEM70 and specific antibodies. TMEM70 is synthesized as a 29kDa precursor protein that is processed to a 21kDa mature form. Immunocytochemical detection of TMEM70 showed mitochondrial colocalization with MitoTracker Red and ATP synthase. Western blot of subcellular fractions revealed the highest signal of TMEM70 in isolated mitochondria and mitochondrial location was confirmed by mass spectrometry analysis. Based on analysis of submitochondrial fractions, TMEM70 appears to be located in the inner mitochondrial membrane, in accordance with predicated transmembrane regions in the central part of the TMEM70 sequence. Two-dimensional electrophoretic analysis did not show direct interaction of TMEM70 with assembled ATP synthase but indicated the presence of dimeric form of TMEM70. No TMEM70 protein could be found in cells and isolated mitochondria from patients with ATP synthase deficiency due to TMEM70 c.317-2A>G mutation thus confirming that TMEM70 biosynthesis is prevented in these patients.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Membrane Proteins Limits: Animals / Humans Language: En Journal: Biochim Biophys Acta Year: 2011 Type: Article Affiliation country: Czech Republic

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Membrane Proteins Limits: Animals / Humans Language: En Journal: Biochim Biophys Acta Year: 2011 Type: Article Affiliation country: Czech Republic