Biochemical, cell biological and immunological issues surrounding the endoplasmic reticulum chaperone GRP94/gp96

被引:118
作者
Nicchitta, CV [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
关键词
D O I
10.1016/S0952-7915(98)80039-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The past year has born witness to compelling demonstrations of the utility of peptide complexes with glucose regulated protein 94 (GRP94, also known as gp96) in cancer immunotherapy. Insights into the structural basis of peptide binding to GRP94 have been obtained and the role of the transporter for antigen presentation in defining the GRP94-bound peptide composition has been determined.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 52 条
[11]   Direct delivery of exogenous MHC class I molecule-binding oligopeptides to the endoplasmic reticulum of viable cells [J].
Day, PM ;
Yewdell, JW ;
Porgador, A ;
Germain, RN ;
Bennink, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8064-8069
[12]   ASSOCIATION OF HSP47, GRP78, AND GRP94 WITH PROCOLLAGEN SUPPORTS THE SUCCESSIVE OR COUPLED ACTION OF MOLECULAR CHAPERONES [J].
FERREIRA, LR ;
NORRIS, K ;
SMITH, T ;
HEBERT, C ;
SAUK, JJ .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (04) :518-526
[13]   PEPTIDE BINDING AND RELEASE BY PROTEINS IMPLICATED AS CATALYSTS OF PROTEIN ASSEMBLY [J].
FLYNN, GC ;
CHAPPELL, TG ;
ROTHMAN, JE .
SCIENCE, 1989, 245 (4916) :385-390
[14]  
GUPTA RS, 1995, MOL BIOL EVOL, V12, P1063
[15]  
KIM YK, 1987, J CELL PHYSL, V133, P533
[16]  
KOCH GLE, 1988, J CELL SCI, V90, P485
[17]   EFFICIENT MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I PRESENTATION OF EXOGENOUS ANTIGEN UPON PHAGOCYTOSIS BY MACROPHAGES [J].
KOVACSOVICSBANKOWSKI, M ;
CLARK, K ;
BENACERRAF, B ;
ROCK, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :4942-4946
[18]   Multiple molecular chaperones complex with misfolded large oligomeric glycoproteins in the endoplasmic reticulum [J].
Kuznetsov, G ;
Chen, LB ;
Nigam, SK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (05) :3057-3063
[19]   Protein disulfide isomerase is the dominant acceptor for peptides translocated into the endoplasmic reticulum [J].
Lammert, E ;
Stevanovic, S ;
Brunner, J ;
Rammensee, HG ;
Schild, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (07) :1685-1690
[20]   The endoplasmic reticulum resident stress protein gp96 binds peptides translocated by TAP [J].
Lammert, E ;
Arnold, D ;
Nijenhuis, M ;
Momburg, F ;
Hammerling, GJ ;
Brunner, J ;
Stevanovic, S ;
Rammensee, HG ;
Schild, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (04) :923-927