Dauterive R, Laroux S, Bunn R C, Chaisson A, Sanson T, Reed B C
Department of Biochemistry and Molecular Biology, Louisiana State University School of Medicine, Shreveport 71130, USA.
J Biol Chem. 1996 May 10;271(19):11414-21. doi: 10.1074/jbc.271.19.11414.
Turnover numbers for 3-O-methylglucose transport by the homologous glucose transporters GLUT1 and GLUT4 were compared to those for truncated and chimeric transporters expressed in Xenopus oocytes to assess potential regulatory properties of the C-terminal domain. The ability of high intracellular sugar concentrations to increase the turnover number for sugar entry ("accelerated exchange") by GLUT1 and not by GLUT4 was maintained in oocytes. Replacing the GLUT1 C terminus with that of GLUT4 stimulated turnover 1.6-fold, but abolished accelerated exchange. Thus, the GLUT1 C terminus permits accelerated exchange by GLUT1, but in doing so must interact with other GLUT1 specific sequences since the GLUT4ctrm1 chimera did not exhibit this kinetic property. Removal of 38 C-terminal amino acids from GLUT4 reduced its turnover number by 40%, whereas removing only 20 residues or replacing its C terminus with that of GLUT1 increased its turnover number 3.5-3.9 fold. Therefore, using mechanisms independent of those which alter transporter targeting to the plasma membrane, C-terminal mutations in either GLUT1 or GLUT4 can activate transport normally restricted by the native C-terminal domain. These results implicate the C termini as targets of physiological factors, which through covalent modification or direct binding might alter C-terminal interactions to regulate intrinsic GLUT1 and GLUT4 transporter activity.
将同源葡萄糖转运蛋白GLUT1和GLUT4转运3 - O - 甲基葡萄糖的转换数与非洲爪蟾卵母细胞中表达的截短型和嵌合型转运蛋白的转换数进行比较,以评估C末端结构域的潜在调节特性。在卵母细胞中,高细胞内糖浓度增加GLUT1而非GLUT4的糖进入转换数(“加速交换”)的能力得以维持。用GLUT4的C末端替换GLUT1的C末端可使转换数提高1.6倍,但消除了加速交换。因此,GLUT1的C末端允许GLUT1进行加速交换,但这样做时必须与其他GLUT1特异性序列相互作用,因为GLUT4ctrm1嵌合体未表现出这种动力学特性。从GLUT4中去除38个C末端氨基酸使其转换数降低40%,而仅去除20个残基或用GLUT1的C末端替换其C末端则使其转换数增加3.5 - 3.9倍。因此,通过与改变转运蛋白靶向质膜的机制无关的机制,GLUT1或GLUT4中的C末端突变可激活通常受天然C末端结构域限制的转运。这些结果表明C末端是生理因子的作用靶点,这些生理因子可能通过共价修饰或直接结合来改变C末端相互作用,从而调节GLUT1和GLUT4转运蛋白的内在活性。