Literature DB >> 9601031

rRNA chemical groups required for aminoglycoside binding.

S C Blanchard1, D Fourmy, R G Eason, J D Puglisi.   

Abstract

Through an affinity chromatography based modification-interference assay, we have identified chemical groups within Escherichia coli 16S ribosomal RNA sequence that are required for binding the aminoglycoside antibiotic paromomycin. Paromomycin was covalently linked to solid support via a nine atom spacer from the 6"'-amine of ring IV, and chemical modifications to an A-site oligonucleotide that disrupted binding were identified. Positions in the RNA oligonucleotide that correspond to G1405(N7), G1491(N7), G1494(N7), A1408(N7), A1493(N7), A1408(N1), A1492(N1), and A1493(N1), as well as the pro-R phosphate oxygens of A1492 and A1493 in 16S rRNA are chemical groups that are essential for a high-affinity RNA-paromomycin interaction. These data are consistent with genetic, biochemical, and structural studies related to neomycin-class antibiotics and provide additional information for establishing an exact model for their interaction with the ribosome.

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Year:  1998        PMID: 9601031     DOI: 10.1021/bi973125y

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  8 in total

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Authors:  Maciej Długosz; Jan M Antosiewicz; Joanna Trylska
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4.  Binding of tobramycin leads to conformational changes in yeast tRNA(Asp) and inhibition of aminoacylation.

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5.  The designer aminoglycoside NB84 significantly reduces glycosaminoglycan accumulation associated with MPS I-H in the Idua-W392X mouse.

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7.  In vivo labelling of functional ribosomes reveals spatial regulation during starvation in Podospora anserina.

Authors:  H Lalucque; P Silar
Journal:  BMC Genet       Date:  2000-11-16       Impact factor: 2.797

8.  Structural origins of gentamicin antibiotic action.

Authors:  S Yoshizawa; D Fourmy; J D Puglisi
Journal:  EMBO J       Date:  1998-11-16       Impact factor: 11.598

  8 in total

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