Cell-free synthesis of membrane subunits of ATP synthase in phospholipid bicelles: NMR shows subunit a fold similar to the protein in the cell membrane

Protein Science

Volumn 21, Issue 2, 2012, Pages 279-288

  Uhlemann, Eva Maria E ^a   Pierson, Hannah E ^a   Fillingame, Robert H ^b   Dmitriev, Oleg Y ^a  

^a UNIVERSITY OF SASKATCHEWAN   (Canada)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

ATP synthase; Cell free synthesis; Membrane protein; Protein NMR

Indexed keywords

AMINO ACID; ISOTOPE; MEMBRANE PROTEIN; PHOSPHATIDYLCHOLINE; PHOSPHOLIPID; PROTON; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ARTICLE; CELL FREE SYSTEM; CELL MEMBRANE; ENZYME SUBUNIT; ENZYME SYNTHESIS; ESCHERICHIA COLI; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLASMID; PRIORITY JOURNAL; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; PURIFICATION;

BACTERIAL PROTON-TRANSLOCATING ATPASES; CELL MEMBRANE; CELL-FREE SYSTEM; ESCHERICHIA COLI PROTEINS; MEMBRANE PROTEINS; MICELLES; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHOSPHOLIPIDS; PROTEIN FOLDING; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; PROTEIN SUBUNITS; PROTON-TRANSLOCATING ATPASES;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 84856192298     PISSN: 09618368     EISSN: 1469896X     Source Type: Journal    
DOI: 10.1002/pro.2014     Document Type: Article

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