Formation of reversible disulfide bonds with the protein matrix of the endoplasmic reticulum correlates with the retention of unassembled Ig light chains

EMBO Journal

Volumn 15, Issue 9, 1996, Pages 2077-2085

  Reddy, Padmalatha ^a,b   Sparvoli, Antonella ^a   Fagioli, Claudio ^a   Fassina, Giorgio ^c   Sitia, Roberto ^a,d  

^a SAN RAFFAELE HOSPITAL   (Italy)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c Biopharmaceuticals   (Italy)

^d UNIVERSITY OF GENOA   (Italy)

Author keywords

Disulfide bonds; Endoplasmic reticulum; Immunoglobulin light chains; Protein matrix

Indexed keywords

ASPARTIC ACID; CYSTEINE; GLYCINE; IMMUNOGLOBULIN LIGHT CHAIN; LYSINE; MUTANT PROTEIN; N ETHYLMALEIMIDE;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DISULFIDE BOND; ENDOPLASMIC RETICULUM; GOLGI COMPLEX; HUMAN; HUMAN CELL; INTRACELLULAR TRANSPORT; ISOTOPE LABELING; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN SECRETION;

EID: 0029944851     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.1460-2075.1996.tb00561.x     Document Type: Article

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