Endoplasmic reticulum-localized amyloid β-peptide is degraded in the cytosol by two distinct degradation pathways

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Volumn 5, Issue 2, 2004, Pages 89-101

  Schmitz, Anton ^a   Schneider, Andrea ^a   Kummer, Markus P ^a,b   Herzog, Volker ^a  

^a UNIVERSITY OF BONN   (Germany)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Amyloid peptide; Endoplasmic reticulum; Insulin degrading enzyme; Protein degradation; Protein translocation

Indexed keywords

ADENOSINE TRIPHOSPHATE; AMYLOID BETA PROTEIN; INSULINASE; MEMBRANE PROTEIN; PROTEASOME; RNA; SECRETORY PROTEIN;

ANIMAL CELL; BRAIN MICROSOME; CELL FREE SYSTEM; CONTROLLED STUDY; CYTOSOL; ENDOPLASMIC RETICULUM; ENZYME REGULATION; ENZYME SUBSTRATE; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; MEMBRANE RECONSTITUTION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEGRADATION; PROTEIN FOLDING; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; REVIEW; RNA INTERFERENCE; SIGNAL TRANSDUCTION;

ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; AMYLOID BETA-PROTEIN; ANIMALS; BRAIN; CHO CELLS; CRICETINAE; CYSTEINE ENDOPEPTIDASES; CYTOPLASM; ENDOPLASMIC RETICULUM; HELA CELLS; HUMANS; INSULYSIN; MEMBRANE PROTEINS; MICROSOMES; MOLECULAR SEQUENCE DATA; MULTIENZYME COMPLEXES; PEPTIDE FRAGMENTS; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN SORTING SIGNALS; PROTEIN TRANSPORT; RNA INTERFERENCE; SWINE;

EID: 1042292018     PISSN: 13989219     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0854.2004.00159.x     Document Type: Review

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