Literature DB >> 12643896

Inhibition of bacterial IF2 binding to fMet-tRNA((fMet)) by aminoglycosides.

J M Evans1, B A Turner, S Bowen, A M Ho, R W Sarver, E Benson, C N Parker.   

Abstract

Screening for inhibitors of bacterial protein synthesis Initiation Factor 2 (IF2) binding to N-formyl-Methionyl-transfer RNA (fMet-tRNA((fMet))) identified a series of aminoglycosides, that included amikacin and kanamycin A1, as inhibitors of this interaction. Subsequent testing revealed that aminoglycosides displayed a wide range of inhibitory activity. However, the failure of these compounds to completely inhibit binding of IF2 to fMet-tRNA((fMet)), the known ability of aminoglycosides to bind RNA, and the ability of the aminoglycosides to displace PicoGreen bound to fMet-tRNA((fMet)) suggest these compounds act by binding fMet-tRNA((fMet)). This hypothesis is further supported by isothermal denaturation experiments that failed to show any interaction between the IF2 protein and the aminoglycosides.

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Year:  2003        PMID: 12643896     DOI: 10.1016/s0960-894x(03)00085-4

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Specific, efficient, and selective inhibition of prokaryotic translation initiation by a novel peptide antibiotic.

Authors:  Letizia Brandi; Attilio Fabbretti; Anna La Teana; Monica Abbondi; Daniele Losi; Stefano Donadio; Claudio O Gualerzi
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-27       Impact factor: 11.205

  1 in total

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