INTERACTION OF PEPTIDES DERIVED FROM THE FAS LIGAND WITH THE FYN-SH3 DOMAIN

被引:45
作者
HANE, M
LOWIN, B
PEITSCH, M
BECKER, K
TSCHOPP, J
机构
[1] UNIV LAUSANNE, INST BIOCHEM, CH-1066 EPALINGES, SWITZERLAND
[2] GLAXO INST MOLEC BIOL, CH-1028 PLAN LES OUATES, SWITZERLAND
关键词
FYN; SH3; DOMAIN; FAS LIGAND; APO-1; APOPTOSIS;
D O I
10.1016/0014-5793(95)01051-F
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
Interaction of the widely expressed Pas with its membrane-bound ligand (Fast) leads to rapid cell death via apoptosis. To avoid pathological tissue damage, the activity of Fast requires tight regulation, Here, we report that the Src homology 3 (SH3) domain of Fyn binds to the proline-rich cytoplasmic region of Fast, Binding of the SH3 domain occurs between amino acid residues 44-71 which contains several potential SH3 interaction sites, This binding is specific, as SH3 domains of Lck, Grb2 and ras-GAP bind only weakly or not at all. We suggest that Fast activity may be modulated by SH3 domains of the src-like Fyn kinase.
引用
收藏
页码:265 / 268
页数:4
相关论文
共 22 条
[1]   THE ROLE OF PROTEIN-TYROSINE KINASES AND PROTEIN-TYROSINE PHOSPHATASES IN T-CELL ANTIGEN RECEPTOR SIGNAL-TRANSDUCTION [J].
CHAN, AC ;
DESAI, DM ;
WEISS, A .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :555-592
[2]   2 BINDING ORIENTATIONS FOR PEPTIDES TO THE SRC SH3 DOMAIN - DEVELOPMENT OF A GENERAL-MODEL FOR SH3-LIGAND INTERACTIONS [J].
FENG, SB ;
CHEN, JK ;
YU, HT ;
SIMON, JA ;
SCHREIBER, SL .
SCIENCE, 1994, 266 (5188) :1241-1247
[3]   CD4-P56LCK ASSOCIATION STUDIED INVIVO USING ANTIBODY-INDUCED CAPPING AND DOUBLE INDIRECT IMMUNOFLUORESCENCE MICROSCOPY [J].
GASSMANN, M ;
AMREIN, KE ;
BURN, P .
JOURNAL OF RECEPTOR RESEARCH, 1993, 13 (1-4) :711-724
[4]   THE GTPASE DYNAMIN BINDS TO AND IS ACTIVATED BY A SUBSET OF SH3 DOMAINS [J].
GOUT, I ;
DHAND, R ;
HILES, ID ;
FRY, MJ ;
PANAYOTOU, G ;
DAS, P ;
TRUONG, O ;
TOTTY, NF ;
HSUAN, J ;
BOOKER, GW ;
CAMPBELL, ID ;
WATERFIELD, MD .
CELL, 1993, 75 (01) :25-36
[5]   FAS AND PERFORIN PATHWAYS AS MAJOR MECHANISMS OF T-CELL-MEDIATED CYTOTOXICITY [J].
KAGI, D ;
VIGNAUX, F ;
LEDERMANN, B ;
BURKI, K ;
DEPRAETERE, V ;
NAGATA, S ;
HENGARTNER, H ;
GOLSTEIN, P .
SCIENCE, 1994, 265 (5171) :528-530
[6]   2 DISTINCT PATHWAYS OF SPECIFIC KILLING REVEALED BY PERFORIN MUTANT CYTOTOXIC T-LYMPHOCYTES [J].
KOJIMA, H ;
SHINOHARA, N ;
HANAOKA, S ;
SOMEYASHIROTA, Y ;
TAKAGAKI, Y ;
OHNO, H ;
SAITO, T ;
KATAYAMA, T ;
YAGITA, H ;
OKUMURA, K ;
SHINKAI, Y ;
ALT, FW ;
MATSUZAWA, A ;
YONEHARA, S ;
TAKAYAMA, H .
IMMUNITY, 1994, 1 (05) :357-364
[7]   REGULATION OF APOPTOSIS IN THE IMMUNE-SYSTEM [J].
KRAMMER, PH ;
BEHRMANN, I ;
DANIEL, P ;
DHEIN, J ;
DEBATIN, KM .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (02) :279-289
[8]   CELL BIOLOGY OF CYTO-TOXIC AND HELPER T-CELL FUNCTIONS - IMMUNOFLUORESCENCE MICROSCOPIC STUDIES OF SINGLE CELLS AND CELL COUPLES [J].
KUPFER, A ;
SINGER, SJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1989, 7 :309-337
[9]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[10]   STRUCTURAL DETERMINANTS OF PEPTIDE-BINDING ORIENTATION AND OF SEQUENCE SPECIFICITY IN SH3 DOMAINS [J].
LIM, WA ;
RICHARDS, FM ;
FOX, RO .
NATURE, 1994, 372 (6504) :375-379