Lysophospholipid-containing membranes modulate the fibril formation of the repeat domain of a human functional amyloid, Pmel17

Journal of Molecular Biology

Volumn 426, Issue 24, 2014, Pages 4074-4086

  Jiang, Zhiping ^a   Lee, Jennifer C ^a  

^a NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

lysolipids; melanosome; protein lipid interaction; TEM; tryptophan

Indexed keywords

AMYLOID; LYSOPHOSPHOLIPID; MELANOCYTE PROTEIN PMEL 17; MICELLE; PMEL PROTEIN, HUMAN;

AMINO ACID SEQUENCE; CELL MEMBRANE; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; CIRCULAR DICHROISM; GENETICS; HUMAN; KINETICS; MELANOSOME; METABOLISM; MICELLE; MOLECULAR GENETICS; PH; PROTEIN CONFORMATION; PROTEIN TERTIARY STRUCTURE; SEQUENCE HOMOLOGY; SPECTROFLUOROMETRY; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE;

AMINO ACID SEQUENCE; AMYLOID; CELL MEMBRANE; CIRCULAR DICHROISM; GP100 MELANOMA ANTIGEN; HUMANS; HYDROGEN-ION CONCENTRATION; KINETICS; LYSOPHOSPHOLIPIDS; MELANOSOMES; MICELLES; MICROSCOPY, ELECTRON, TRANSMISSION; MODELS, CHEMICAL; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; PROTEIN CONFORMATION; PROTEIN STRUCTURE, TERTIARY; SEQUENCE HOMOLOGY, AMINO ACID; SPECTROMETRY, FLUORESCENCE;

EID: 84914094530     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2014.10.009     Document Type: Article

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