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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 74 (1969), S. 103-116 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Partially purified preparations of two protein factors, one of which is stable at 50°C (FIs) and the other unstable at 50°C (FIu), are required for the GTP-dependent, mRNA-directed binding of aminoacyl-tRNA to ribosomes, as well as for polypeptide synthesis in the presence of a third factor, FII. Both FIs and FIu are required for maximal interaction with GTP to form a GTP•protein complex that subsequently interacts with aminoacyl-tRNA, but not with deacylated tRNA or with N-(substituted)-aminoacyl-tRNA, to form an aminoacyl-tRNA•GTP•protein complex. A mixture of FIs and FIu also interacts with GDP to form a GDP•protein complex; however, no subsequent interaction with aminoacyl-tRNA is observed. In addition to aminoacyl-tRNA and GTP, Mg2+ and NH4+ are required for the formation of the aminoacyl-tRNA•GTP•protein complex. Although both protein factors, FIs and FIu, are required for the formation of this complex, only the heat-labile protein, FIu, is a component of the complex. Very little dissociation of the GTP moiety of the complex occurs in the presence of Mg2+, and no detectable exchange is observed with GTP, GDP, or Pi. In contrast, appreciable dissociation of the aminoacyl-tRNA from the GTP•protein occurs even in the presence of Mg2+, and exchange with other aminoacyl-tRNA's can be readily demonstrated. In the absence of Mg2+, complete dissociation of both the GTP and the aminoacyl-tRNA from the protein occurs. Evidence has been obtained to demonstrate that the aminoacyl-tRNA•GTP•protein complex is an intermediate in the GTP-dependent binding of aminoacyl-tRNA to ribosomes. The binding of the aminoacyl-tRNA to the ribosome occurs with the concomitant formation of Pi and a GDP • protein complex. Incorporation of the bound aminoacyl-tRNA into polypeptide requires additional GTP and the third transfer factor, FII.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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