PH-DEPENDENCE AND EXCHANGE OF HIGH AND LOW RESPONDER PEPTIDES BINDING TO A CLASS-II MHC MOLECULE

被引:89
作者
REAY, PA [1 ]
WETTSTEIN, DA [1 ]
DAVIS, MM [1 ]
机构
[1] STANFORD UNIV, DEPT MICROBIOL & IMMUNOL, STANFORD, CA 94305 USA
关键词
BINDING; CLASS-II MHC; EXCHANGE; PEPTIDE; PH;
D O I
10.1002/j.1460-2075.1992.tb05350.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have compared the binding kinetics of two antigenic peptides to a soluble class II MHC molecule. One of the peptides provokes a strong T cell response and the other a much weaker one. Both show greatly increased (approximately 40-fold) association rates at pH 5 in comparison to neutral pH, consistent with the low pH environment of late endosomes being most conducive to class II MHC - peptide binding. Interestingly, the weak peptide has a much faster off-rate that is significantly increased at pH 5 and it can be entirely replaced in an exchange reaction by the stronger one. This suggests that one characteristic of immunodominant peptides is that of nearly irreversible binding, such that they will be strongly selected for in the course of class II MHC transit and recycling through endosomal compartments. Modelling the parameters of this peptide exchange also suggests that a large fraction of the GPI-chimeric MHC molecules used in this study are 'empty' with respect to endogenous peptides, or else occupied with extremely weak ones, consistent with their inability to load processed peptides intracellularly.
引用
收藏
页码:2829 / 2839
页数:11
相关论文
共 58 条
[11]   BINDING OF LABELED INFLUENZA MATRIX PEPTIDE TO HLA DR IN LIVING B-LYMPHOID CELLS [J].
CEPPELLINI, R ;
FRUMENTO, G ;
FERRARA, GB ;
TOSI, R ;
CHERSI, A ;
PERNIS, B .
NATURE, 1989, 339 (6223) :392-394
[12]  
CHESNUT RW, 1986, ADV IMMUNOL, V39, P51
[13]   PROCESSED ANTIGEN BINDS TO NEWLY SYNTHESIZED MHC CLASS II MOLECULES IN ANTIGEN-SPECIFIC LYMPHOCYTES-B [J].
DAVIDSON, HW ;
REID, PA ;
LANZAVECCHIA, A ;
WATTS, C .
CELL, 1991, 67 (01) :105-116
[14]   T-CELL RECEPTOR GENE DIVERSITY AND SELECTION [J].
DAVIS, MM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :475-496
[15]   THE MINIMAL NUMBER OF CLASS-II MHC ANTIGEN COMPLEXES NEEDED FOR T-CELL ACTIVATION [J].
DEMOTZ, S ;
GREY, HM ;
SETTE, A .
SCIENCE, 1990, 249 (4972) :1028-1030
[16]   CHARACTERIZATION OF ANTIGEN ASSOCIATION WITH ACCESSORY CELLS - SPECIFIC REMOVAL OF PROCESSED ANTIGENS FROM THE CELL-SURFACE BY PHOSPHOLIPASES [J].
FALO, LD ;
HABER, SI ;
HERRMANN, S ;
BENACERRAF, B ;
ROCK, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (02) :522-526
[17]  
FERGUSON MAJ, 1988, ANNU REV BIOCHEM, V57, P285
[18]   CO-LOCALIZATION OF MOLECULES INVOLVED IN ANTIGEN PROCESSING AND PRESENTATION IN AN EARLY ENDOCYTIC COMPARTMENT [J].
GUAGLIARDI, LE ;
KOPPELMAN, B ;
BLUM, JS ;
MARKS, MS ;
CRESSWELL, P ;
BRODSKY, FM .
NATURE, 1990, 343 (6254) :133-139
[19]   TURNOVER OF IA PEPTIDE COMPLEXES IS FACILITATED IN VIABLE ANTIGEN-PRESENTING CELLS - BIOSYNTHETIC TURNOVER OF IA VS PEPTIDE EXCHANGE [J].
HARDING, CV ;
ROOF, RW ;
UNANUE, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) :4230-4234
[20]   FUNCTIONAL AND ULTRASTRUCTURAL EVIDENCE FOR INTRACELLULAR FORMATION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II-PEPTIDE COMPLEXES DURING ANTIGEN PROCESSING [J].
HARDING, CV ;
UNANUE, ER ;
SLOT, JW ;
SCHWARTZ, AL ;
GEUZE, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5553-5557