Atypical recognition consensus of CIN85/SETA/Ruk SH3 domains revealed by target-assisted iterative screening

被引:49
作者
Kurakin, AV [1 ]
Wu, S [1 ]
Bredesen, DE [1 ]
机构
[1] Buck Inst Age Res, Novato, CA 94945 USA
关键词
D O I
10.1074/jbc.M305264200
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
Target-assisted iterative screening applied to random peptide libraries unveiled a novel and atypical recognition consensus shared by CIN85/SETA/Ruk SH3 domains, PX(P/A) XXR. Confirmed by mutagenesis and in vitro binding experiments, the novel consensus allowed for the accurate mapping of CIN85 SH3 binding sites within known CIN85 interactors, c-Cbl, BLNK, Cbl-b, AIP1/Alix, SB1, and CD2 proteins, as well as the prediction of CIN85 novel-interacting partners in protein databases. Synaptojanin 1, PAK2, ZO-2, and TAF(II)70, which contain CIN85 SH3 recognition consensus sites, were selectively precipitated from mouse brain lysates by CIN85 SH3 domains in glutathione S-transferase pull-down experiments. A direct interaction of synaptojanin 1 and PAK2 with CIN85 SH3 domains was confirmed by Far Western blotting.
引用
收藏
页码:34102 / 34109
页数:8
相关论文
共 42 条
[21]   Structural basis for specific binding of the gads SH3 domain to an RxxK motif-containing SLP-76 peptide: A novel mode of peptide recognition [J].
Liu, Q ;
Berry, D ;
Nash, P ;
Pawson, T ;
McGlade, CJ ;
Li, SSC .
MOLECULAR CELL, 2003, 11 (02) :471-481
[22]   A cortactin-CD2-associated protein (CD2AP) complex provides a novel link between epidermal growth factor receptor endocytosis and the actin cytoskeleton [J].
Lynch, DK ;
Winata, SC ;
Lyons, RJ ;
Hughes, WE ;
Lehrbach, GM ;
Wasinger, V ;
Corthals, G ;
Cordwell, S ;
Daly, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21805-21813
[23]   PAK kinases are directly coupled to the PIX family of nucleotide exchange factors [J].
Manser, E ;
Loo, TH ;
Koh, CG ;
Zhao, ZS ;
Chen, XQ ;
Tan, L ;
Tan, I ;
Leung, T ;
Lim, L .
MOLECULAR CELL, 1998, 1 (02) :183-192
[24]   Signalling to and from tight junctions [J].
Matter, K ;
Balda, MS .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (03) :225-236
[25]  
Mayer BJ, 2001, J CELL SCI, V114, P1253
[26]   A novel peptide-SH3 interaction [J].
Mongiovi, AM ;
Romano, PR ;
Panni, S ;
Mendoza, M ;
Wong, WT ;
Musacchio, A ;
Cesareni, G ;
Di Fiore, PP .
EMBO JOURNAL, 1999, 18 (19) :5300-5309
[27]   HIGH-RESOLUTION CRYSTAL-STRUCTURES OF TYROSINE KINASE SH3 DOMAINS COMPLEXED WITH PROLINE-RICH PEPTIDES [J].
MUSACCHIO, A ;
SARASTE, M ;
WILMANNS, M .
NATURE STRUCTURAL BIOLOGY, 1994, 1 (08) :546-551
[28]   Exploiting the basis of proline recognition by SH3 and WW domains: Design of n-substituted inhibitors [J].
Nguyen, JT ;
Turck, CW ;
Cohen, FE ;
Zuckermann, RN ;
Lim, WA .
SCIENCE, 1998, 282 (5396) :2088-2092
[29]   Assembly of cell regulatory systems through protein interaction domains [J].
Pawson, T ;
Nash, P .
SCIENCE, 2003, 300 (5618) :445-452
[30]   The endophilin-CIN85-Cbl complex mediates ligand-dependent downregulation of c-Met [J].
Petrelli, A ;
Gilestro, GF ;
Lanzardo, S ;
Comoglio, PM ;
Migone, N ;
Giordano, S .
NATURE, 2002, 416 (6877) :187-190