The majority of H2-M3 is retained intracellularly in a peptide-receptive state and traffics to the cell surface in the presence of N-formylated peptides

Journal of Experimental Medicine

Volumn 190, Issue 3, 1999, Pages 423-434

  Chiu, Nancy M ^a   Chun, Taehoon ^a   Fay, Miriam ^a   Mandal, Manas ^a,b   Wang, Chyung Ru ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Antigen presentation; Cytotoxic T cells; Major histocompatibility complex class I; N formylated peptides; Rodent

Indexed keywords

CD1 ANTIGEN; H2 ANTIGEN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; MONOCLONAL ANTIBODY; PEPTIDE DERIVATIVE;

ANIMAL CELL; ANTIGEN PRESENTATION; ANTIGEN PRESENTING CELL; ARTICLE; CHIMERA; CYTOTOXIC T LYMPHOCYTE; ENDOPLASMIC RETICULUM; GOLGI COMPLEX; HUMAN; HUMAN CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN TRANSPORT;

ANIMALS; ANTIBODIES, MONOCLONAL; ANTIGEN PRESENTATION; ATP-BINDING CASSETTE TRANSPORTERS; BIOLOGICAL TRANSPORT; CELL LINE; CELL MEMBRANE; CRICETINAE; HISTOCOMPATIBILITY ANTIGENS CLASS I; INTRACELLULAR FLUID; KINETICS; LYMPHOID TISSUE; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; N-FORMYLMETHIONINE; OLIGOPEPTIDES; PROTEIN SYNTHESIS INHIBITORS;

EID: 0033517126     PISSN: 00221007     EISSN: None     Source Type: Journal    
DOI: 10.1084/jem.190.3.423     Document Type: Article

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