Literature DB >> 6162473

Distances between 3' ends of ribosomal ribonucleic acids reassembled into Escherichia coli ribosomes.

O W Odom, D J Robbins, J Lynch, D Dottavio-Martin, G Kramer, B Hardesty.   

Abstract

The three ribonucleic acids (RNAs) from Escherichia coli ribosomes were isolated and then labeled at their 3' ends by oxidation with periodate followed by reaction with thiosemicarbazides of fluorescein or eosin. Ribosomal subunits reconstituted with the labeled RNAs were active for polyphenylalanine synthesis. The distances between the 3' ends of the RNAs in 70S ribosomes were estimated by nonradiative energy transfer from fluorescein to eosin. The percentage of energy transfer was calculated from the decrease in fluorescence lifetime of fluorescein in the quenched sample compared to the unquenched sample. Fluorescence lifetime was measured in real time by using a mode-locked laser for excitation and a high-speed electrostatic photomultiplier tube for detection of fluorescence. The distances between fluorophores attached to the 3' ends of 16S RNA and 5S RNA or 23S RNA were estimated to be about 55 and 71 A, respectively. The corresponding distance between the 5S RNA and 23S RNA was too large to be measured reliably with the available probes but was estimated to be greater than 65 A. Comparison of the quantum yields of the labeled RNAs free in solution and reconstituted into ribosomal subunits suggests that the 3' end of 16S RNA does not interact appreciably with other ribosomal components and may be in a relatively exposed position, whereas the 3' ends of the 5S RNA and 23S RNA may be buried in the 70S ribosomal subunit.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6162473     DOI: 10.1021/bi00567a001

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


  19 in total

1.  The estimation of distances between specific backbone-labeled sites in DNA using fluorescence resonance energy transfer.

Authors:  H Ozaki; L W McLaughlin
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

2.  Protein synthesis by single ribosomes.

Authors:  Francesco Vanzi; Serguei Vladimirov; Charlotte R Knudsen; Yale E Goldman; Barry S Cooperman
Journal:  RNA       Date:  2003-10       Impact factor: 4.942

3.  DNA-catalyzed reactivity of a phosphoramidate functional group and formation of an unusual pyrophosphoramidate linkage.

Authors:  Amit Sachdeva; Scott K Silverman
Journal:  Org Biomol Chem       Date:  2011-11-01       Impact factor: 3.876

4.  Trypanosoma brucei 20 S editosomes have one RNA substrate-binding site and execute RNA unwinding activity.

Authors:  Cordula Böhm; Venkata Subbaraju Katari; Michael Brecht; H Ulrich Göringer
Journal:  J Biol Chem       Date:  2012-06-01       Impact factor: 5.157

5.  Efficient RNA 5'-adenylation by T4 DNA ligase to facilitate practical applications.

Authors:  Yangming Wang; Scott K Silverman
Journal:  RNA       Date:  2006-04-17       Impact factor: 4.942

6.  Theory of measurement of Förster-type energy transfer in macromolecules.

Authors:  B Epe; K G Steinhäuser; P Woolley
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

7.  Chemical methods of DNA and RNA fluorescent labeling.

Authors:  D Proudnikov; A Mirzabekov
Journal:  Nucleic Acids Res       Date:  1996-11-15       Impact factor: 16.971

8.  Fluorimetric distance determination by resonance energy transfer. Ribosome-bound transfer RNA.

Authors:  K Friedrich; P Woolley; K G Steinhäuser
Journal:  Eur Biophys J       Date:  1988       Impact factor: 1.733

Review 9.  Structure and function of ribosomal RNA.

Authors:  R Brimacombe; W Stiege
Journal:  Biochem J       Date:  1985-07-01       Impact factor: 3.857

10.  Localization of 3' ends of 5S and 23S rRNAs in reconstituted subunits of Escherichia coli ribosomes.

Authors:  M Stöffler-Meilicke; G Stöffler; O W Odom; A Zinn; G Kramer; B Hardesty
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.