AI Article Synopsis

  • Aminoglycoside antibiotics bind to the A site of 16S ribosomal RNA, leading to misreading of the genetic code and inhibiting the process of translocation during protein synthesis.
  • Researchers determined the structures of an A site RNA oligonucleotide both in isolation and when bound to aminoglycosides like paromomycin and gentamicin C1a using NMR techniques.
  • The study compares the high-precision NMR structure of the oligonucleotide-paromomycin complex with the X-ray crystal structure of the 30S ribosomal subunit, highlighting significant differences at position A1493 and confirming the critical interactions that influence ribosome function.

Article Abstract

Aminoglycoside antibiotics that bind to 16S ribosomal RNA in the aminoacyl-tRNA site (A site) cause misreading of the genetic code and inhibit translocation. Structures of an A site RNA oligonucleotide free in solution and bound to the aminoglycosides paromomycin or gentamicin C1a have been determined by NMR. Recently, the X-ray crystal structure of the entire 30S subunit has been determined, free and bound to paromomycin. Distinct differences were observed in the crystal structure, particularly at A1493. Here, the NMR structure of the oligonucleotide-paromomycin complex was determined with higher precision and is compared with the X-ray crystal structure of the 30S subunit complex. The comparison shows the validity of both structures in identifying critical interactions that affect ribosome function.

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Source
http://dx.doi.org/10.1016/s0969-2126(02)00934-6DOI Listing

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