Case R D, Piccione E, Wolf G, Benett A M, Lechleider R J, Neel B G, Shoelson S E
Joslin Diabetes Center, Boston, Massachusetts 02215.
J Biol Chem. 1994 Apr 8;269(14):10467-74.
Signaling by tyrosine kinases involves direct associations between proteins with Src homology 2 (SH2) domains and sites of tyrosine phosphorylation. Specificity in signaling pathways results in part from inherent selectivity in interactions between particular SH2 domains and phosphopeptide sequences. The cytoplasmic phosphotyrosine phosphatase SH-PTP2 (Syp, PTP 1D, PTP-2C) contains two SH2 domains (N and C) which mediate its association with and activation by the platelet-derived growth factor (PDGF) and epidermal growth factor receptors and IRS-1. We have developed a competitive phosphopeptide binding assay to analyze specificity of the SH-PTP2 N-SH2 domain for phosphorylation sites of these phosphoproteins. The sequence surrounding Tyr1009 bound with greatest affinity (ID50 = 14 microM) of eight PDGF receptor-derived phosphopeptides tested. No peptides corresponding to known epidermal growth factor receptor phosphorylation sites bound with high affinity. However, an alternative sequence surrounding Tyr954 bound tightly (ID50 = 21 microM). Of the 13 IRS-1-related peptides analyzed, sequences surrounding Tyr546, Tyr895, and Tyr1172 bound with highest affinity (ID50 = 11, 4, and 1 microM, respectively). Alternative phosphopeptides generally bound with much weaker affinity (ID50 > 150 microM). These findings are consistent with recent mutational analyses of the PDGF receptor and predict site-specific interactions between SH-PTP2 and each of these phosphoproteins. Comparisons between peptide sequences suggest that the N-terminal SH2 domain of SH-PTP2 binds with highest affinity to phosphotyrosine (pY) followed by a beta-branched residue (Val, Ile, Thr) at pY+1 and a hydrophobic residue (Val, Leu, Ile) at pY+3 positions. Peptide truncation studies also indicate that residues outside of the pY-1 to pY+4 motif are required for high affinity interactions.
酪氨酸激酶信号传导涉及具有Src同源2(SH2)结构域的蛋白质与酪氨酸磷酸化位点之间的直接关联。信号通路的特异性部分源于特定SH2结构域与磷酸肽序列之间相互作用的固有选择性。细胞质酪氨酸磷酸酶SH-PTP2(Syp、PTP 1D、PTP-2C)包含两个SH2结构域(N和C),它们介导其与血小板衍生生长因子(PDGF)、表皮生长因子受体和IRS-1的结合及激活。我们开发了一种竞争性磷酸肽结合测定法,以分析SH-PTP2 N-SH2结构域对这些磷蛋白磷酸化位点的特异性。在测试的八个PDGF受体衍生的磷酸肽中,围绕Tyr1009的序列结合亲和力最高(ID50 = 14 microM)。没有与已知表皮生长因子受体磷酸化位点相对应的肽以高亲和力结合。然而,围绕Tyr954的另一个序列紧密结合(ID50 = 21 microM)。在分析的13个IRS-1相关肽中,围绕Tyr546、Tyr895和Tyr1172的序列结合亲和力最高(ID50分别为11、4和1 microM)。替代磷酸肽通常以弱得多的亲和力结合(ID50 > 150 microM)。这些发现与最近对PDGF受体的突变分析一致,并预测了SH-PTP2与这些磷蛋白中每一个之间的位点特异性相互作用。肽序列之间的比较表明,SH-PTP2的N端SH2结构域与磷酸酪氨酸(pY)结合亲和力最高,其次是pY+1处的β分支残基(Val、Ile、Thr)和pY+3处的疏水残基(Val、Leu、Ile)。肽截短研究还表明,pY-1至pY+4基序之外的残基是高亲和力相互作用所必需的。