Rackoff W R, Rubin R A, Earp H S
Mol Cell Endocrinol. 1984 Feb;34(2):113-9. doi: 10.1016/0303-7207(84)90062-5.
The 170 000 dalton hepatic epidermal growth factor (EGF) receptor is phosphorylated on serine and tyrosine residues. The evidence indicates that distinct protein kinases are involved. Since EGF and agents that elevate cAMP are believed to participate in the regulation of liver regeneration, we tested whether or not the catalytic subunit of cAMP-dependent protein kinase (catalytic subunit), a known serine kinase, would utilize the EGF receptor as a substrate. The catalytic subunit increased phosphorylation of the EGF receptor in purified rat liver plasma membranes. The serine specificity of the catalytic subunit was established by phosphoamino acid analysis of electrophoretically purified EGF receptor. The result was confirmed by catalytic subunit phosphorylation of affinity purified preparations of the EGF receptor. The rates of dephosphorylation of the membrane-associated EGF receptor phosphorylated on different residues were compared. Dephosphorylation of serine residues (after catalytic subunit phosphorylation) was considerably slower (t1/2 greater than 120 sec) than the removal of phosphotyrosine after stimulation with EGF (t1/2 less than 30 sec).
170000道尔顿的肝表皮生长因子(EGF)受体在丝氨酸和酪氨酸残基上发生磷酸化。证据表明涉及不同的蛋白激酶。由于EGF和提高cAMP的试剂被认为参与肝再生的调节,我们测试了cAMP依赖性蛋白激酶的催化亚基(催化亚基),一种已知的丝氨酸激酶,是否会将EGF受体用作底物。催化亚基增加了纯化的大鼠肝质膜中EGF受体的磷酸化。通过对电泳纯化的EGF受体进行磷酸氨基酸分析确定了催化亚基的丝氨酸特异性。通过对亲和纯化的EGF受体制剂进行催化亚基磷酸化证实了该结果。比较了在不同残基上磷酸化的膜相关EGF受体的去磷酸化速率。丝氨酸残基(催化亚基磷酸化后)的去磷酸化比EGF刺激后磷酸酪氨酸的去除(t1/2小于30秒)要慢得多(t1/2大于120秒)。