AbstractWe have previously developed [(1987) Biochemistry 26, 5200–5208] the use of trans-diamminedichloroplatinum(II) to induce reversible RNA-protein crosslinks in the ribosomal 30 S subunit. Protein S18 and, to a lesser extent, proteins S13/S14, S11, S4 and S3 could be crosslinked to the 16 S rRNA. The aim of the present work was to identify the crosslinking sites of protein S18. Three sites could be detected: a major one located in region 825–858, and two others located in regions 434–500 and 233–297. This result is discussed in the light of current knowledge of the topographical localization of S18 in the 30 S subunit and of its relation with function
A series of P-site probes, chlorambucilyl-(Pro)-Phe-tRNA, were pre-pared and reacted with poly(U)-di...
AbstractThe E. coli 16 S rRNA with single-site breaks centered at position 777 or 785 was obtained b...
To gain a better understanding of the architecture of the ribosome in general, and the structure of ...
AbstractWe have previously developed [(1987) Biochemistry 26, 5200–5208] the use of trans-diamminedi...
Abstract30 S protein-16 S rRNA crosslinking by reaction with 1-ethyl-3-dimethylaminopropylcarbodiimi...
AbstractThe 30S ribosomal P site serves several functions in translation. It must specifically bind ...
AbstractTranslation initiation complexes consisting of 30S ribosomal subunits, 32P-labelled mRNA (00...
AbstractThe cleavable homobifunctional reagent dichloro[N,N,N′,N′-tetrakis(2-aminoethyl)-1,6-hexamet...
AbstractRibosomal proteins participating in intersubunit RNA-protein contacts (directly interacting ...
AbstractrRNA-protein cross-links in free E. Coli35S-labeled 70 S ribosomes and in the initiation com...
(1) N-Acetyl{(\u273)H}lysyl-tRNA(\u27Lys) and N-acetyl{(\u273)H}glutamyl-tRNA(,2)(\u27Glu) were cros...
AbstractSaccharomyces carlsbergensis 60 S ribosomal subunits were treated with the hetero-bifunction...
AbstractEscherichia coli 50 S ribosomal subunits were reconstituted with and without protein L16 pre...
Evidence is presented in three separate cases for the forma-tion of RNA-RNA cross-links in intact E....
AbstractRNA—protein interactions in the 60 S subunits of rat liver ribosomes were studied using 1-et...
A series of P-site probes, chlorambucilyl-(Pro)-Phe-tRNA, were pre-pared and reacted with poly(U)-di...
AbstractThe E. coli 16 S rRNA with single-site breaks centered at position 777 or 785 was obtained b...
To gain a better understanding of the architecture of the ribosome in general, and the structure of ...
AbstractWe have previously developed [(1987) Biochemistry 26, 5200–5208] the use of trans-diamminedi...
Abstract30 S protein-16 S rRNA crosslinking by reaction with 1-ethyl-3-dimethylaminopropylcarbodiimi...
AbstractThe 30S ribosomal P site serves several functions in translation. It must specifically bind ...
AbstractTranslation initiation complexes consisting of 30S ribosomal subunits, 32P-labelled mRNA (00...
AbstractThe cleavable homobifunctional reagent dichloro[N,N,N′,N′-tetrakis(2-aminoethyl)-1,6-hexamet...
AbstractRibosomal proteins participating in intersubunit RNA-protein contacts (directly interacting ...
AbstractrRNA-protein cross-links in free E. Coli35S-labeled 70 S ribosomes and in the initiation com...
(1) N-Acetyl{(\u273)H}lysyl-tRNA(\u27Lys) and N-acetyl{(\u273)H}glutamyl-tRNA(,2)(\u27Glu) were cros...
AbstractSaccharomyces carlsbergensis 60 S ribosomal subunits were treated with the hetero-bifunction...
AbstractEscherichia coli 50 S ribosomal subunits were reconstituted with and without protein L16 pre...
Evidence is presented in three separate cases for the forma-tion of RNA-RNA cross-links in intact E....
AbstractRNA—protein interactions in the 60 S subunits of rat liver ribosomes were studied using 1-et...
A series of P-site probes, chlorambucilyl-(Pro)-Phe-tRNA, were pre-pared and reacted with poly(U)-di...
AbstractThe E. coli 16 S rRNA with single-site breaks centered at position 777 or 785 was obtained b...
To gain a better understanding of the architecture of the ribosome in general, and the structure of ...