THE CONVERSION OF EIF-2.GDP TO EIF-2.GTP BY EIF-2B REQUIRES MET-TRANSFER RNAFMET

被引:15
作者
GROSS, M
RUBINO, MS
HESSEFORT, SM
机构
[1] Department of Pathology, The University of Chicago, Chicago, IL 60637
关键词
D O I
10.1016/0006-291X(91)92109-W
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 investigated why the recycling of eIF-2·GDP to eIF-2·GTP, mediated by the guanine nucleotide exchange factor eIF-2B, is rapid in rabbit reticulocyte lysate, reconstituted for optimal protein synthesis, but slow in an isolated reaction with purified eIF-2B. We have found that purified eIF-2B dissociates eIF-2·[3H]GDP as efficiently in the presence of GTP as it does in the presence of GDP provided Met-tRNAfMet is added. tRNAfMed is ineffective, and there is no Met-tRNAfMet requirement for exchange with GDP. Exchange of eIF-2 bound GDP for GTP is completely dependent upon Met-tRNAfMet in the presence of ATP, suggesting that under physiological conditions efficient recycling of eIF-2·GDP to eIF-2·GTP requires conversion of the latter, a relatively unstable complex, to a more stable Met-tRNAfMet·eIF-2·GTP complex. © 1991.
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页码:1500 / 1507
页数:8
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共 34 条
[11]  
GROSS M, 1988, J BIOL CHEM, V263, P12486
[13]  
GROSS M, 1989, J BIOL CHEM, V264, P21879
[14]  
GROSS M, 1980, J BIOL CHEM, V255, P6270
[15]  
GROSS M, 1979, J BIOL CHEM, V254, P2370
[16]   CHARACTERIZATION OF A RABBIT RETICULOCYTE SUPERNATANT FACTOR THAT REVERSES THE TRANSLATIONAL INHIBITION OF HEMIN DEFICIENCY [J].
GROSS, M ;
WATTMORSE, P ;
KAPLANSKY, DA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 654 (02) :219-226
[17]   CONTROL OF PROTEIN-SYNTHESIS BY HEMIN - ISOLATION AND CHARACTERIZATION OF A SUPERNATANT FACTOR FROM RABBIT RETICULOCYTE LYSATE [J].
GROSS, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 447 (04) :445-459
[18]   ADDITIONAL EVIDENCE THAT HEMIN-CONTROLLED TRANSLATIONAL REPRESSOR FROM RABBIT RETICULOCYTES IS A PROTEIN-KINASE [J].
GROSS, M ;
MENDELEWSKI, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 74 (02) :559-569
[19]  
GROSS M, 1991, J CELL BIOCHEM, V15, P194