CHARACTERIZATION OF GLUT3 PROTEIN EXPRESSED IN CHINESE-HAMSTER OVARY CELLS

被引:34
作者
ASANO, T
KATAGIRI, H
TAKATA, K
TSUKUDA, K
LIN, JL
ISHIHARA, H
INUKAI, K
HIRANO, H
YAZAKI, Y
OKA, Y
机构
[1] UNIV TOKYO,FAC MED,DEPT INTERNAL MED 3,TOKYO 113,JAPAN
[2] KYORIN UNIV,SCH MED,DEPT ANAT,MITAKA,TOKYO 181,JAPAN
关键词
D O I
10.1042/bj2880189
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have expressed GLUT3 protein, an isoform of a facilitative glucose transporter, in Chinese hamster ovary cells by transfection of its cDNA using an expression vector. The expressed GLUT3 protein was detected by Western-blot analysis as a broad band of 45-65 kDa, indicating intensive glycosylation of the protein. The expressed GLUT3 protein was observed, by immunofluorescence staining, to be located mainly at the plasma membrane, and its expression was associated with a marked increase in glucose-transport activity. Kinetic analysis revealed that the K(m) value of GLUT3 protein for 3-O-methylglucose uptake was approx. 35% of that of GLUT1 protein, whereas the K(m) value of GLUT3 protein for 2-deoXy-D-glucose uptake was very similar to that of GLUT1 protein. The V(max.) value of GLUT3 protein for 3-O-methylglucose and 2-deoxyglucose uptake was approx. 20-50% of that of GLUT1 protein. GLUT3 protein was well photolabelled with [H-3]cytochalasin B or a mannose derivative, 2-N-4-[H-3](1-azi-2,2,2-trifluoroethyl)benzoyl-1,3-bis-(D-mannos-4-yloxy)-2-propylamine. Thus GLUT3 protein has very similar characteristics to GLUT1 protein including its subcellular localization, but exhibits lower K(m) and V(max.) values for 3-O-methylglucose uptake.
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页码:189 / 193
页数:5
相关论文
共 28 条
[1]  
ASANO T, 1989, J BIOL CHEM, V264, P3416
[2]   CLONING OF A RABBIT BRAIN GLUCOSE TRANSPORTER CDNA AND ALTERATION OF GLUCOSE TRANSPORTER MESSENGER-RNA DURING TISSUE-DEVELOPMENT [J].
ASANO, T ;
SHIBASAKI, Y ;
KASUGA, M ;
KANAZAWA, Y ;
TAKAKU, F ;
AKANUMA, Y ;
OKA, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 154 (03) :1204-1211
[3]   MOLECULAR-BIOLOGY OF MAMMALIAN GLUCOSE TRANSPORTERS [J].
BELL, GI ;
KAYANO, T ;
BUSE, JB ;
BURANT, CF ;
TAKEDA, J ;
LIN, D ;
FUKUMOTO, H ;
SEINO, S .
DIABETES CARE, 1990, 13 (03) :198-208
[4]   TRANSPORT OF SUGARS IN CHICK-EMBRYO FIBROBLASTS - EVIDENCE FOR A LOW-AFFINITY SYSTEM AND A HIGH-AFFINITY SYSTEM FOR GLUCOSE-TRANSPORT [J].
CHRISTOPHER, CW ;
KOHLBACHER, MS ;
AMOS, H .
BIOCHEMICAL JOURNAL, 1976, 158 (02) :439-450
[5]  
CLARKE DD, BASIC NEUROCHEMISTRY, P541
[6]   PHOSPHORYLATION BUT NOT TRANSPORT OF SUGARS IS ENHANCED IN VIRUS-TRANSFORMED MOUSE 3T3 CELLS [J].
COLBY, C ;
ROMANO, AH .
JOURNAL OF CELLULAR PHYSIOLOGY, 1975, 85 (01) :15-23
[7]   KINETICS OF 3-ORTHO-METHYL-D-GLUCOSE TRANSPORT IN ISOLATED RAT HEPATOCYTES [J].
CRAIK, JD ;
ELLIOTT, KRF .
BIOCHEMICAL JOURNAL, 1979, 182 (02) :503-508
[8]   HEXOSE-TRANSPORT IN L6 RAT MYOBLASTS .1. RATE-LIMITING STEP, KINETIC-PROPERTIES, AND EVIDENCE FOR 2 SYSTEMS [J].
DAMORE, T ;
LO, TCY .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 127 (01) :95-105
[9]   BLOOD-BRAIN-BARRIER GLUCOSE TRANSPORTER IS ASYMMETRICALLY DISTRIBUTED ON BRAIN CAPILLARY ENDOTHELIAL LUMENAL AND ABLUMENAL MEMBRANES - AN ELECTRON-MICROSCOPIC IMMUNOGOLD STUDY [J].
FARRELL, CL ;
PARDRIDGE, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) :5779-5783
[10]   RATE-LIMITING STEPS OF 2-DEOXYGLUCOSE UPTAKE IN RAT ADIPOCYTES [J].
FOLEY, JE ;
FOLEY, R ;
GLIEMANN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 599 (02) :689-698