Dean A M, Lee M H, Koshland D E
Department of Biochemistry, University of California, Berkeley 94720.
J Biol Chem. 1989 Dec 5;264(34):20482-6.
Equilibrium binding studies demonstrate that purified Escherichia coli isocitrate dehydrogenase binds isocitrate, alpha-ketoglutarate, NADP, and NADPH at 1:1 ratios of substrate to enzyme monomer. The phosphorylated enzyme, which is completely inactive, is unable to bind isocitrate but retains the ability to bind NADP and NADPH. Replacement of serine 113, which is the site of phosphorylation, by aspartate results in an inactive enzyme that is unable to bind isocitrate. Replacement of the same serine with other amino acids (lysine, threonine, cysteine, tyrosine, and alanine) produces active enzymes that bind both substrates. Hence, the negative charge of an aspartate or a phosphorylated serine at site 113 inactivates the enzyme by preventing the binding of isocitrate.
平衡结合研究表明,纯化的大肠杆菌异柠檬酸脱氢酶以底物与酶单体1:1的比例结合异柠檬酸、α-酮戊二酸、NADP和NADPH。完全无活性的磷酸化酶无法结合异柠檬酸,但保留了结合NADP和NADPH的能力。将作为磷酸化位点的丝氨酸113替换为天冬氨酸会产生一种无活性的酶,该酶无法结合异柠檬酸。用其他氨基酸(赖氨酸、苏氨酸、半胱氨酸、酪氨酸和丙氨酸)替换同一丝氨酸会产生能结合两种底物的活性酶。因此,位点113处天冬氨酸或磷酸化丝氨酸的负电荷通过阻止异柠檬酸的结合使酶失活。