Chemically related 4,5-linked aminoglycoside antibiotics drive subunit rotation in opposite directions Journal Article


Authors: Wasserman, M. R.; Pulk, A.; Zhou, Z.; Altman, R. B.; Zinder, J. C.; Green, K. D.; Garneau-Tsodikova, S.; Doudna Cate, J. H.; Blanchard, S. C.
Article Title: Chemically related 4,5-linked aminoglycoside antibiotics drive subunit rotation in opposite directions
Abstract: Dynamic remodelling of intersubunit bridge B2, a conserved RNA domain of the bacterial ribosome connecting helices 44 (h44) and 69 (H69) of the small and large subunit, respectively, impacts translation by controlling intersubunit rotation. Here we show that aminoglycosides chemically related to neomycin - paromomycin, ribostamycin and neamine - each bind to sites within h44 and H69 to perturb bridge B2 and affect subunit rotation. Neomycin and paromomycin, which only differ by their ring-I 6′-polar group, drive subunit rotation in opposite directions. This suggests that their distinct actions hinge on the 6′-substituent and the drugâ €™ s net positive charge. By solving the crystal structure of the paromomycin-ribosome complex, we observe specific contacts between the apical tip of H69 and the 6′-hydroxyl on paromomycin from within the drugâ €™ s canonical h44-binding site. These results indicate that aminoglycoside actions must be framed in the context of bridge B2 and their regulation of subunit rotation.
Keywords: complex formation; molecular dynamics; bacteria (microorganisms); binding site; crystal structure; drug binding; neomycin; rotation; aminoglycoside antibiotic agent; article; neamine; paromomycin; ribostamycin
Journal Title: Nature Communications
Volume: 6
ISSN: 2041-1723
Publisher: Nature Publishing Group  
Date Published: 2015-07-01
Start Page: 7896
Language: English
DOI: 10.1038/ncomms8896
PROVIDER: scopus
PMCID: PMC4522699
PUBMED: 26224058
DOI/URL:
Notes: Export Date: 2 September 2015 -- Source: Scopus
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  1. John C Zinder
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