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The tightest non-aminoglycoside ligand for the bacterial ribosomal RNA A-site

Date:
October 15, 2018
Source:
Tohoku University
Summary:
A research group has made a significant discovery with positive implications for the development of bacteria-fighting drugs. The aminoacyl-tRNA site (A-site) of the 16S RNA decoding region in the bacterial ribosome looks promising for a new era of antibiotic drug development.
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A research group at Tohoku University has made a significant discovery with positive implications for the development of bacteria-fighting drugs. The aminoacyl-tRNA site (A-site) of the 16S RNA decoding region in the bacterial ribosome looks promising for a new era of antibiotic drug development.

Traditional aminoglycoside antibiotics are problematic given their high toxicity and the potential for resistance development. The research at Tohoku University focused on bacterial A-site binding small ligands whose structures are distinct from the aminoglycoside family, which offer potential for the development of novel drugs that treat bacterial infections with a reduction in the problems associated with traditional antibiotics.

The research group led by Dr. Seiichi Nishizawa and Dr. Yusuke Sato (Department of Chemistry, Graduate School of Science) has reported a novel small ligand, ATMND-C2-NH2 that has the tightest binding affinity for the bacterial A-site among the non-aminoglycoside ligands.

ATMND-C2-NH2 shows a significant fluorescent quenching response upon selective binding to the internal loop of the bacterial (Escherichia coli) A-site-containing model RNA. ATMND-C2-NH2 has also proven useful as an indicator for assessing ligand/A-site interactions.

The results obtained by the research group offer a rational basis for the generation of novel A-site binding ligands with a view toward novel antibiotics with less toxicity and minimum resistance development.


Story Source:

Materials provided by Tohoku University. Note: Content may be edited for style and length.


Journal Reference:

  1. Yusuke Sato, Masafumi Rokugawa, Sho Ito, Sayaka Yajima, Hiroki Sugawara, Norio Teramae, Seiichi Nishizawa. Fluorescent Trimethylated Naphthyridine Derivative with an Aminoalkyl Side Chain as the Tightest Non-aminoglycoside Ligand for the Bacterial A-site RNA. Chemistry - A European Journal, 2018; 24 (52): 13862 DOI: 10.1002/chem.201802320

Cite This Page:

Tohoku University. "The tightest non-aminoglycoside ligand for the bacterial ribosomal RNA A-site." ScienceDaily. ScienceDaily, 15 October 2018. <www.sciencedaily.com/releases/2018/10/181015104542.htm>.
Tohoku University. (2018, October 15). The tightest non-aminoglycoside ligand for the bacterial ribosomal RNA A-site. ScienceDaily. Retrieved April 25, 2024 from www.sciencedaily.com/releases/2018/10/181015104542.htm
Tohoku University. "The tightest non-aminoglycoside ligand for the bacterial ribosomal RNA A-site." ScienceDaily. www.sciencedaily.com/releases/2018/10/181015104542.htm (accessed April 25, 2024).

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