Abstract
It is well established that when E. coli 30S ribosomal subunits are irradiated with ultraviolet light under mild conditions a specific cross-link is formed between protein S7 and the 16S RNA. Methodology is presented for the analysis of the single nucleotide residue concerned in this cross-link. Firstly, the identity of the ribonuclease T1 octanucleotide attached to S7 is confirmed by a new method, which involves isolation and analysis of S7-polynucleotide complexes containing 30 -- 40 nucleotides. Secondly, the isolated S7-octanucleotide complex is digested successively with ribonuclease A, proteinase K and ribonuclease T2, and the nucleotides liberated are identified. The results show unambiguously that uridine residue number 1239 in the 16S RNA sequence is cross-linked to protein S7.
MeSH Terms
Base Sequence
Escherichia coli/analysis
Molecular Weight
Nucleoproteins/analysis
Oligoribonucleotides/analysis
Protein Binding
RNA, Ribosomal/radiation effects
Ribonucleoproteins/analysis
Ribosomal Proteins/radiation effects
Ribosomes/analysis
Ultraviolet Rays
Chemicals
Nucleoproteins
Oligoribonucleotides
RNA, Ribosomal
Ribonucleoproteins
Ribosomal Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zwieb C
Brimacombe R
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