Table 1.
tRNA substrate | Ribosomes or subunits* | Protected bases† | Ref. |
---|---|---|---|
N-Ac-Phe-tRNAPhe | 70S | A1916, A1918, U1926, G2252, G2253, A2439, A2451, G2505, U2506, U2584, U2585, A2602↑‡ | 2 |
CACCA-(Ac-Phe)§ | 70S¶ | G2251‖, G2252, | 3 |
UACCA-(Ac-Leu) | G2253, A2439, | ||
CAACCA-(Ac-Met) | A2451, U2506, U2584, U2585, A2602↑ | ||
N-Ac-Tyr-tRNABiotTyr | 50S** | G2251, G2252, G2253, A2439, A2451, U2506, U2584, U2585 | This paper |
E. coli 70S ribosomes or 50S large ribosomal subunits.
Refers to relative reactivity of individual 23S rRNA bases to chemical modification.
Binding of the P site substrates to 70S ribosomes increases accessibility of A2602 to modification with dimethyl sulfate.
Refers to 3′-terminal fragments generated by RNase T1 hydrolysis of corresponding N-acyl-aminoacyl-tRNAs.
Binding of tRNA fragments to 70S ribosomes was performed in the fragment reaction conditions.
Protection of G2251 was reported in ref. 22.
Binding of biotinylated N-Ac-Tyr-tRNABiotTyr to 50S ribosomal subunits was performed in the fragment reaction conditions.