KIRROMYCIN-INDUCED MODIFICATIONS FACILITATE THE SEPARATION OF EF-TU SPECIES AND REVEAL INTERMOLECULAR INTERACTIONS

被引:20
作者
ANBORGH, PH [1 ]
SWART, GWM [1 ]
PARMEGGIANI, A [1 ]
机构
[1] ECOLE POLYTECH,BIOCHEM LAB,YODOGAWA KU,UNITE SDI 61840,F-91128 PALAISEAU,FRANCE
关键词
PROTEIN SYNTHESIS; ELONGATION FACTOR TU; KIRROMYCIN;
D O I
10.1016/0014-5793(91)80874-3
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
A simplified method for the separation of a kirromycin-sensitive tufB-encoded elongation factor Tu (EF-TuBs) from a kirromycin-resistant tufA product (EF-TuAr) was obtained by exploiting the specific increase of positive charges induced by the antibiotic, resulting in a retarded elution of kirromycin-bound EF-TuBs on ionic chromatography. The kirromycin-free EF-TuBs is active in poly(Phe) synthesis and shows similar properties to EF-TuAsBs. As expected for these two distinct species, the dissociation of the EF-TuArBs.GTP complex in the presence of kirromycin shows a biphasic curve; in contrast, a monophasic GTP dissociation rate was found for a combination of two mutated EF-Tu species, EF-TuArBo, revealing the existence of intermolecular interactions. These observations prove for the first time the existence of cooperative phenomena between EF-Tu species in vitro, as suggested earlier by in vivo experiments.
引用
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页码:232 / 236
页数:5
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