Donella Deana A, Mac Gowan C H, Cohen P, Marchiori F, Meyer H E, Pinna L A
Dipartimento di Chimica Biologica, Universitá di Padova, Italy.
Biochim Biophys Acta. 1990 Feb 19;1051(2):199-202. doi: 10.1016/0167-4889(90)90194-i.
The synthetic phosphopeptide RRATpVA was found to be the most effective substrate for protein phosphatase 2C (PP2C) so far identified. Replacement of phosphothreonine by phosphoserine decreased activity over 20-fold and a striking preference for phosphothreonine was also observed with two other substrates (RRSTpTpVA and casein) that were phosphorylated on both serine and threonine. Replacement of the C-terminal valine in RRATpVA by proline abolished dephosphorylation, while exchanging the N-terminal alanine by proline had no effect. The preference for phosphothreonine and the effect of proline are similar to protein phosphatase 2A (PP2A). However, the peptide RRREEETpEEEAA, an excellent substrate for PP2A, was not dephosphorylated by PP2C, and substitution of the C-terminal valine in RRATpVA by glutamic acid reduced the rate of dephosphorylation by PP2C over 10-fold, without affecting dephosphorylation by PP2A. Addition of two extra N-terminal arginine residues to RRASpVA increased PP2A catalysed dephosphorylation 4- to 5-fold, without altering dephosphorylation by PP2C. These results represent the first study of the specificity of PP2C using synthetic peptides, and strengthen the view that this approach may lead to the development of more effective and specific substrates for the serine/threonine-specific protein phosphatases.
合成磷酸肽RRATpVA被发现是迄今为止所鉴定出的蛋白磷酸酶2C(PP2C)最有效的底物。将磷酸苏氨酸替换为磷酸丝氨酸会使活性降低20倍以上,并且在另外两个丝氨酸和苏氨酸均被磷酸化的底物(RRSTpTpVA和酪蛋白)中也观察到对磷酸苏氨酸有显著偏好。将RRATpVA中的C末端缬氨酸替换为脯氨酸会消除去磷酸化作用,而将N末端丙氨酸替换为脯氨酸则没有影响。对磷酸苏氨酸的偏好以及脯氨酸的作用与蛋白磷酸酶2A(PP2A)相似。然而,PP2A的优良底物肽RRREEETpEEEAA不能被PP2C去磷酸化,并且将RRATpVA中的C末端缬氨酸替换为谷氨酸会使PP2C的去磷酸化速率降低10倍以上,而不影响PP2A的去磷酸化作用。在RRASpVA的N末端添加两个额外的精氨酸残基会使PP2A催化的去磷酸化增加4至5倍,而不会改变PP2C的去磷酸化作用。这些结果代表了使用合成肽对PP2C特异性的首次研究,并强化了这样一种观点,即这种方法可能会导致开发出更有效和特异的丝氨酸/苏氨酸特异性蛋白磷酸酶底物。