APP dimer formation is initiated in the endoplasmic reticulumand differs between APP isoforms

Cellular and Molecular Life Sciences

Volumn 69, Issue 8, 2012, Pages 1353-1375

  Isbert, Simone ^a   Wagner, Katja ^b   Eggert, Simone ^b   Schweitzer, Andrea ^a   Multhaup, Gerd ^c   Weggen, Sascha ^d   Kins, Stefan ^b   Pietrzik, Claus U ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

^b Rheinland Pfälzische Technische Universität Kaiserslautern Landau   (Germany)

^c FREIE UNIVERSITÄT BERLIN   (Germany)

^d HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

APP dimerization; Disulfide bonds; Endoplasmic reticulum; Retention motifs

Indexed keywords

AMYLOID PRECURSOR PROTEIN; CYSTEINE; DIMER; GREEN FLUORESCENT PROTEIN; SERINE PROTEINASE INHIBITOR; APLP1 PROTEIN, HUMAN; ISOPROTEIN;

ANIMAL CELL; ARTICLE; CELL SURFACE; CELLULAR DISTRIBUTION; CHO CELL; CONTROLLED STUDY; DIMERIZATION; DISULFIDE BOND; DROSOPHILA; ENDOPLASMIC RETICULUM; GENETIC TRANSFECTION; INSECT CELL; MOLECULAR CLONING; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN ISOLATION; PROTEIN LOCALIZATION; WESTERN BLOTTING; ANIMAL; CHEMISTRY; HAMSTER; HUMAN; METABOLISM; PROTEIN MULTIMERIZATION; PROTEIN TERTIARY STRUCTURE; ULTRASTRUCTURE;

AMYLOID BETA-PROTEIN PRECURSOR; ANIMALS; CHO CELLS; CRICETINAE; CYSTEINE; ENDOPLASMIC RETICULUM; HUMANS; PROTEIN ISOFORMS; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, TERTIARY;

EID: 84860869183     PISSN: 1420682X     EISSN: 14209071     Source Type: Journal    
DOI: 10.1007/s00018-011-0882-4     Document Type: Article

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