Chiles T C, Laine R O, Shay N F, Handlogten M E, Nick H S, Kilberg M S
Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, Gainesville 32610.
Biochem Biophys Res Commun. 1993 Jun 30;193(3):1068-75. doi: 10.1006/bbrc.1993.1734.
Biosynthesis of several rat liver proteins is enhanced by amino acid deprivation of cultured hepatocytes or hepatoma cells. One of these proteins, MP-73, was synthesized at a rate 2- to 3-fold greater when cells were incubated for 3-9 h under conditions of amino acid deprivation versus amino acid supplementation. Immunoblotting with polyclonal antibodies prepared against MP-73 localized it to the inner mitochondrial membrane. MP-73 appears to be a hydrophobic, integral membrane protein. MP-73 antibody was used to identify a partial cDNA (NS3.2) of approximately 2 kb. A probe prepared from pNS3.2 identified a transcript in rat Fao hepatoma cells of approximately 4.4 kb that was increased in abundance by more than 20-fold following amino acid starvation of the cells.
培养的肝细胞或肝癌细胞中氨基酸缺乏会增强几种大鼠肝脏蛋白质的生物合成。其中一种蛋白质MP-73,当细胞在氨基酸缺乏条件下培养3至9小时时,其合成速率比在氨基酸补充条件下快2至3倍。用针对MP-73制备的多克隆抗体进行免疫印迹分析,将其定位到线粒体内膜。MP-73似乎是一种疏水性整合膜蛋白。MP-73抗体用于鉴定一个约2 kb的部分cDNA(NS3.2)。从pNS3.2制备的探针在大鼠Fao肝癌细胞中鉴定出一个约4.4 kb的转录本,在细胞氨基酸饥饿后其丰度增加了20倍以上。