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Immunoelectron Microscopy of Ribosomes Carrying a Fluorescence Label in a Defined Position. Location of Proteins S17 and L6 in the Ribosome of Escherichia Coli

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Journal FEBS Lett
Specialty Biochemistry
Date 1983 Oct 31
PMID 6354754
Citations 4
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Abstract

By coupling fluorescein to a defined amino acid of a single ribosomal protein and incorporating this protein into the ribosome, we have obtained ribosomes labelled at a single, defined position. A fluorescein-specific antibody preparation was used to locate the fluorescein residues bound to the two cysteines at positions 58 and 63 of protein S17 and to the cysteine at position 86 of protein L6. This study demonstrates the advantages which accrue from the combination of electron microscopy and fluorimetry.

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Characterisation of a mutant from Escherichia coli lacking protein L15 and localisation of protein L15 by immuno-electron microscopy.

Lotti M, Dabbs E, Hasenbank R, Stoffler-Meilicke M, Stoffler G Mol Gen Genet. 1983; 192(3):295-300.

PMID: 6197616 DOI: 10.1007/BF00392165.


Location of protein S4 on the small ribosomal subunit of E. coli and B. stearothermophilus with protein- and hapten-specific antibodies.

Stoffler-Meilicke M, Epe B, Woolley P, Lotti M, Littlechild J, Stoffler G Mol Gen Genet. 1984; 197(1):8-18.

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Localization of ribosomal protein L27 at the peptidyl transferase centre of the 50 S subunit, as determined by immuno-electron microscopy.

Lotti M, Stoffler-Meilicke M, Stoffler G Mol Gen Genet. 1987; 210(3):498-503.

PMID: 3123891 DOI: 10.1007/BF00327203.


Localization of proteins L4, L5, L20 and L25 on the ribosomal surface by immuno-electron microscopy.

Lotti M, Noah M, Stoffler-Meilicke M, Stoffler G Mol Gen Genet. 1989; 216(2-3):245-53.

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