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Exploration of the L18 binding site on 5S RNA by deletion mutagenesis

  • Yale University

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Several deletion variants of E. coli 5S RNA have been constructed and produced either in vivo or in vitro using T7 RNA Polymerase. Their structures and ribosomal protein L18 binding properties have been examined. All of them are similar to wild-type 5S RNA in their helix II-III regions, where L18 binds [Huber, P.W. and Wool, LG. (1984) Proc. Natl. Acad. Sci. (USA) 81, 322-326; Douthwaite, S., Christensen, A., and Garrett, R.A. (1982) Biochemistry 21, 2313-2320.], by NMR criteria. However, none of the molecules examined that lack the helix IV-helix V stem bind L18 efficiendy, even though that portion of 5S RNA is outside tbe L18 footprint. Tbe L18 binding site is clearly more than a simple hairpin loop.

Original languageEnglish
Pages (from-to)10717-10732
Number of pages16
JournalNucleic Acids Research
Volume16
Issue number22
DOIs
StatePublished - Nov 25 1988

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