ApoA-I mimetic peptides with differing ability to inhibit atherosclerosis also exhibit differences in their interactions with membrane bilayers

Journal of Biological Chemistry

Volumn 282, Issue 3, 2007, Pages 1980-1988

  Handattu, Shaila P ^a   Garber, David W ^a,c   Horn, Dawn C ^a   Hughes, Donald W ^b   Berno, Bob ^b   Bain, Alex D ^b   Mishra, Vinod K ^a   Palgunachari, Mayakonda N ^a   Datta, Geeta ^a   Anantharamaiah, G M ^a   Epand, Richard M ^b  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b MCMASTER UNIVERSITY   (Canada)

^c University of Alabama at Birmingham   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMPHIPATHIC HELIX; ANTI-INFLAMMATORY ACTIVITY; APOA-I MIMETIC PEPTIDES; ATHEROSCLEROSIS; INTRAPERITONEAL INJECTION; LIPOPROTEIN; MEMBRANE BILAYERS; METHYL GROUP;

AROMATIC HYDROCARBONS; DISEASE CONTROL; LIPID BILAYERS; MOLECULAR BIOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

PEPTIDES;

APOLIPOPROTEIN A1; APOLIPOPROTEIN B; AROMATIC COMPOUND; CARBON 14; HIGH DENSITY LIPOPROTEIN; METHYL GROUP; PEPTIDE 3F; PEPTIDE 3F 2; PEPTIDE DERIVATIVE; PHOSPHOLIPID; PROTON; SODIUM CHLORIDE; UNCLASSIFIED DRUG; CARBON; LIPOPROTEIN; PEPTIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIINFLAMMATORY ACTIVITY; ARTICLE; ATHEROSCLEROSIS; BILAYER MEMBRANE; BIOLOGICAL ACTIVITY; CONTROLLED STUDY; DRUG BLOOD LEVEL; DRUG DISTRIBUTION; DRUG EFFECT; DRUG ELIMINATION; DRUG HALF LIFE; FEMALE; ISOTOPE LABELING; MAXIMUM ALLOWABLE CONCENTRATION; MOTION; MOUSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NULL ALLELE; PHOSPHOLIPID BILAYER; PRIORITY JOURNAL; ANIMAL; BIOMIMETICS; C57BL MOUSE; CHEMICAL STRUCTURE; CHEMISTRY; LIPID BILAYER; METABOLISM; PROTEIN BINDING;

MUS;

ANIMALS; APOLIPOPROTEIN A-I; ATHEROSCLEROSIS; BIOMIMETICS; CARBON; FEMALE; LIPID BILAYERS; LIPOPROTEINS; MAGNETIC RESONANCE SPECTROSCOPY; MICE; MICE, INBRED C57BL; MODELS, MOLECULAR; PEPTIDES; PHOSPHOLIPIDS; PROTEIN BINDING;

EID: 33847318289     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M606231200     Document Type: Article

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