5S Ribonucleic acid-protein complex extracted from rat liver ribosomes by formamide

Biochemistry ◽  
1972 ◽  
Vol 11 (12) ◽  
pp. 2323-2326 ◽  
Author(s):  
Mary L. Petermann ◽  
Mary G. Hamilton ◽  
Amalia Pavlovec
Biochemistry ◽  
1973 ◽  
Vol 12 (20) ◽  
pp. 3859-3865 ◽  
Author(s):  
Joan S. Tscherne ◽  
Bernard Weinstein ◽  
Karl W. Lanks ◽  
Naola B. Gersten ◽  
Charles R. Cantor

1972 ◽  
Vol 126 (4) ◽  
pp. 923-931 ◽  
Author(s):  
J. Hradec

1. Transferase I of rat liver binds aminoacyl-tRNA to form a relatively stable complex, which is retained on cellulose nitrate filters. This reaction proceeds at both 0°C and 37°C and is inhibited by GTP. The resulting product is stabilized by GTP and Mg2+. 2. Only very low quantities of deacylated tRNA are bound by transferase I. 3. Methods are described for the preparative isolation of the transferase I–aminoacyl-tRNA complex from incubation mixtures by using ion-exchange procedures. 4. The transferase I–aminoacyl-tRNA complex becomes readily bound to ribosomes. The presence of Mg2+ is essential for the binding. GTP stimulates this reaction but is not absolutely required. 5. It is concluded that the formation of the transferase I–aminoacyl-tRNA complex may be the primary reaction in the binding of aminoacyl-tRNA to mammalian ribosomes and that, unlike in bacterial systems, GTP is not absolutely required for this step.


1975 ◽  
Vol 145 (2) ◽  
pp. 169-176 ◽  
Author(s):  
M Ariatti ◽  
A O Hawtrey

1. Cyclohexylpuromycin, an anlogue of puromycin in which a cyclohexane ring replaces the aromatic benzene ring of the L-phenylalanyl moeity of the nucleoside., has been synthesized and examined for its ability to release N-acetylphenylalanine from tRNA attached to rat liver ribosomes. 2.dl-Cyclohexylpuromycin was active in reacting with N-[3H]acetylphenylalanyl-tRNA on rat liver ribosomes to form N-E13H]lacetylphenylalanycyclohexypuromycin. 3. The reaction product N-acetylphenylalanylcyclohexylpuromycin and the corresponding analogue N-acetylphenylalanylpuromycin were chemically synthesized for evaluation of the structure of the released N-acetylphenylalanyl-containing material. 4. The results obtained suggest that the model of Raacke (1971) for purmycin reactivity needs further examination with regard to the role played by the aromatic ring system of the Lphenylalanyl moiety of the nucleoside


1964 ◽  
Vol 91 (3) ◽  
pp. 21C-32C ◽  
Author(s):  
A. J. Munro

Nature ◽  
1963 ◽  
Vol 199 (4892) ◽  
pp. 489-490 ◽  
Author(s):  
A. KORNER ◽  
A. J. MUNRO

RNA ◽  
2008 ◽  
Vol 14 (3) ◽  
pp. 491-502 ◽  
Author(s):  
W. Chang ◽  
R. F. Zaarour ◽  
S. Reck-Peterson ◽  
J. Rinn ◽  
R. H. Singer ◽  
...  

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